The role of 1,3-dithianes in natural product synthesis (Q57099056)

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Generation and synthetic applications of 2-lithio-1,3-dithianes

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Methods of Reactivity Umpolung

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Umpolung of the Reactivity of Carbonyl Compounds Through Sulfur-Containing Reagents

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Antibiotika aus Gleitenden Bakterien, XXVI. Konstitution und absolute Konfiguration der epimeren Myxovirescine A1 und A2

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

ML-236A, ML-236B, and ML-236C, new inhibitors of cholesterogenesis produced by Penicillium citrinium

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Crystal and molecular structure of compactin, a new antifungal metabolite from Penicillium brevicompactum

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Structure of FK506, a novel immunosuppressant isolated from Streptomyces

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

FK-506, a novel immunosuppressant isolated from a Streptomyces. I. Fermentation, isolation, and physico-chemical and biological characteristics

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Octalactins A and B: cytotoxic eight-membered-ring lactones from a marine bacterium, Streptomyces sp

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Histrionicotoxins: roentgen-ray analysis of the novel allenic and acetylenie spiroalkaloids isolated from a Colombian frog, Dendrobates histrionicus

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Pinnatoxin A: a toxic amphoteric macrocycle from the Okinawan bivalve Pinna muricata

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

A stereoselective synthesis of the C10-C31 (BCDEF ring) portion of pinnatoxin A

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

An efficient route to 3-deoxy-d-manno-2-octulosonic acid (KDO) derivatives via a 1,4-cyclic sulfate approach

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

First Total Synthesis of the Re-Type Lipopolysaccharide This work was supported by the Research for the Future Program (No. 97L00502) from the Japan Society for the Promotion of Science. H.Y. is grateful for a JSPS Research Fellowship for Young Scie

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Stereocontrolled total synthesis of the Stemona alkaloid (-)-stenine

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Asymmetric synthesis of the northern half C1-C16 of the bryostatins

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Versatile 8-oxabicyclo[3.2.1]oct-6-en-3-one: stereoselective methodology for generating C-glycosides, delta-valerolactones, and polyacetate segments

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

An enantio- and stereocontrolled synthesis of (-)-mycestericin E via cinchona alkaloid-catalyzed asymmetric Baylis-Hillman reaction

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Fungal metabolites. Part 14. Novel potent immunosuppressants, mycestericins, produced by Mycelia sterilia

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Determination of absolute configuration and biological activity of new immunosuppressants, mycestericins D, E, F and G

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Metabolic products of microorganisms. 224. Bafilomycins, a new group of macrolide antibiotics. Production, isolation, chemical structure and biological activity

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

The structure of the bafilomycins, a new group of macrolide antibiotics

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Total synthesis of bafilomycin A(1) relying on iterative 1,2-induction in acyclic precursors

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

A New Antifungal Substance of Fungal Origin

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

The isolation, identification, and bioassay of the antifungal metabolites produced by Monocillium nordinii

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Concise asymmetric syntheses of radicicol and monocillin I.

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Synthesis of gem-dideuterated tetradecanoic acids and their use in investigating the enzymatic transformation of (Z)-11-tetradecenoic acid into (E,E)-10,12-tetradecadienoic acid

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Pinellic acid from the tuber of Pinellia ternata Breitenbach as an effective oral adjuvant for nasal influenza vaccine

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Sex pheromone components of the spring hemlock looper,Lambdina athasaria (Walker) (Lepidoptera: Geometridae).

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Dioxolane-to-bridged acetal-to-spiroketal via ring-closing metathesis and rearrangement: a novel route to 1,7-dioxaspiro[5.5]undecanes

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

A formal total synthesis of leucascandrolide A

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Design, synthesis, and evaluation of 6-carboxyalkyl and 6-phosphonoxyalkyl derivatives of 7-oxo-8-ribitylaminolumazines as inhibitors of riboflavin synthase and lumazine synthase

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Manzamine A, a novel antitumor alkaloid from a sponge

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Synthesis of the ABC ring system of manzamine A.

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Tedanolide: a potent cytotoxic macrolide from the Caribbean sponge Tedania ignis

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Synthesis of tedanolide and 13-deoxytedanolide. Assembly of a common C(1)-C(11) subtarget

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Total synthesis of (+)-13-deoxytedanolide

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Dithiane additions to vinyl epoxides: steric control over the SN2 and SN2' manifolds

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Hennoxazoles, bioactive bisoxazoles from a marine sponge

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Aplysiatoxin and debromoaplysiatoxin, constituents of the marine mollusk Stylocheilus longicauda

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Pironetin, a novel plant growth regulator produced by Streptomyces sp. NK10958. I. Taxonomy, production, isolation and preliminary characterization.

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Pironetin, a novel plant growth regulator produced by Streptomyces sp. NK10958. II. Structural elucidation

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

A new antibiotic, tautomycin

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Bioactive marine metabolites. Part 16. Calyculin A. A novel antitumor metabolite from the marine sponge Discodermia calyx

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Discodermolide: a new bioactive polyhydroxylated lactone from the marine sponge Discodermia dissoluta

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Gram-scale synthesis of (+)-discodermolide

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Total synthesis of the antiviral marine natural product (-)-hennoxazole A

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Kurzilactone from Cryptocarya kurzii

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Fostriecin, an antitumor antibiotic with inhibitory activity against serine/threonine protein phosphatases types 1 (PP1) and 2A (PP2A), is highly selective for PP2A.

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Purification of protein phosphatase 4 catalytic subunit: inhibition by the antitumour drug fostriecin and other tumour suppressors and promoters

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Total Synthesis of Fostriecin (CI-920) We thank Professor Andrew G. Myers and Scott E. Schaus for helpful discussions, and Dr. Alexandra E. Gould and Isabel K. Reichardt for important preliminary experimental work. We also thank Dr. Robert J. Schult

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Apicularens A and B, new cytostatic macrolides from Chondromyces species (myxobacteria): production, physico-chemical and biological properties

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Apicularen A and B, Cytotoxic 10-Membered Lactones with a Novel Mechanism of Action fromChondromyces Species (Myxobacteria): Isolation, Structure Elucidation, and Biosynthesis

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Synthesis of the core structure of apicularen a by transannular cyclization

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Multicomponent linchpin couplings of silyl dithianes: synthesis of the Schreiber C(16-28) trisacetonide subtarget for mycoticins A and B

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

The Spongistatins: Architecturally Complex Natural Products-Part One: A Formal Synthesis of (+)-Spongistatin 1 by Construction of an Advanced ABCD Fragment Financial support was provided by the National Institutes of Health (National Cancer Institut

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

The Spongistatins: Architecturally Complex Natural Products-Part Two: Synthesis of the C(29-51) Subunit, Fragment Assembly, and Final Elaboration to (+)-Spongistatin 2

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Spongistatin synthetic studies. An efficient, second-generation construction of an advanced ABCD intermediate

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Control of olefin geometry in the bryostatin B-ring through exploitation of a C(2)-symmetry breaking tactic and a Smith-Tietze coupling reaction

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Total synthesis of (+)-spongistatin 1. An effective second-generation construction of an advanced EF Wittig salt, fragment union, and final elaboration

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Galbonolides A and B--two non-glycosidic antifungal macrolides

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Total Synthesis of (+)-Zaragozic Acid C

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

The Synthesis of CP-263,114 and CP-225,917: Striking Long-Range Stereocontrol in the Fashioning of C7 Financial support was provided by the National Institutes of Health (Grant nos. CA-28824 and HL-25848 for S.J.D., CA-08748 for the Sloan-Kettering

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Total Synthesis of the CP Molecules CP-263,114 and CP-225,917- Part 1: Synthesis of Key Intermediates and Intelligence Gathering

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Total synthesis of the CP-molecules (CP-263,114 and CP-225,917, phomoidrides B and A). 1. Racemic and asymmetric synthesis of bicyclo[4.3.1] key building blocks

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Total synthesis of the CP-molecules (CP-263,114 and CP-225,917, phomoidrides B and A). 2. Model studies for the construction of key structural elements and first-generation strategy

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Total synthesis of the CP-molecules (CP-263,114 and CP-225,917, phomoidrides B and A). 3. Completion and synthesis of advanced analogues

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

The CP molecule labyrinth: a paradigm of how endeavors in total synthesis lead to discoveries and inventions in organic synthesis

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Ciguatoxin: isolation and chemical nature

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Reactions of metallated 1,3-dithianes with carboxylic acid derivatives

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Studies on marine microorganisms. IV. A new antibiotic SS-228 Y produced by Chainia isolated from shallow sea mud

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Total synthesis of aplasmomycin

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

12-Oxo-LTB4, a Key Pivotal Intermediate in LTB4 Metabolism

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

The regioselectivity of addition of organolithium reagents to enones and enals: the role of HMPA.

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Synthetic Applications of 2-(1,3-Dithian-2-yl)indoles. 7. Synthesis of Aspidospermidine

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Acylvinyl and vinylogous synthons

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Deprotecting dithiane-containing alkaloids

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Stereodivergent synthesis of enantiopure cis- and trans-3-Ethyl-4-piperidineacetates

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

trans-Addition of two carbon substituents across a benzene double bond in [(eta6-benzene)Mo(CO)3].

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Ptilocaulin and isoptilocaulin, antimicrobial and cytotoxic cyclic guanidines from the Caribbean sponge Ptilocaulis aff. P. spiculifer (Lamarck, 1814)

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

The structure of roflamycoin, a new polyene macrolide antifungal antibiotic

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Lasiodiplodin, a potent antileukemic macrolide from Euphorbia splendens

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Enantioselective synthesis of attenols A and B

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

A diastereoselective intramolecular hydroamination approach to the syntheses of (+)-, (+/-)-, and (-)-pinidinol

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Organolanthanide-catalyzed intramolecular hydroamination/cyclization of amines tethered to 1,2-disubstituted alkenes

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Azaspiracid, a New Marine Toxin Having Unique Spiro Ring Assemblies, Isolated from Irish Mussels,Mytilus edulis

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Synthesis of the ABCD Ring System of Azaspiracid We thank Drs. D. H. Huang and G. Siuzdak for NMR spectroscopic and mass spectrometric assistance, respectively. This work was financially supported by the National Institutes of Health (USA), The Skag

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Synthesis and Determination of the Absolute Configuration of Pyrenophorin and Vermiculin

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Phyllanthocin, a novel bisabolane aglycone from the antileukemic glycoside, phyllanthoside

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

X-Ray crystal structure of rocaglamide, a novel antileulemic 1H-cyclopenta[b]benzofuran from Aglaia elliptifolia

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Total Synthesis of Apoptolidin: Part 2. Coupling of Key Building Blocks and Completion of the Synthesis We thank Dr. C. Khosla and Dr. Y. Hayakawa for generous gifts of apoptolidin, and Dr. D. H. Huang and Dr. G. Siuzdak for NMR spectroscopic and ma

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Apoptolidin, a new apoptosis inducer in transformed cells from Nocardiopsis sp

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Total Synthesis of Apoptolidin: Part 1. Retrosynthetic Analysis and Construction of Building Blocks We thank Dr. D. H. Huang and Dr. G. Siuzdak for NMR spectroscopic and mass spectrometric assistance, respectively. This work was financially supporte

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Total Synthesis of (-)-Maytansinol.

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Letter: A revised structure of vermiculine. A novel macrolide dilactone antibiotic from Penicillium vermiculatum.

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Novel antibiotics, furaquinocins A and B. Taxonomy, fermentation, isolation and physico-chemical and biological characteristics.

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Mevinolin: a highly potent competitive inhibitor of hydroxymethylglutaryl-coenzyme A reductase and a cholesterol-lowering agent

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Cationic cyclization of ketene dithioacetals. A general synthesis of pyrrolizidine, indolizidine, and quinolizidine alkaloid ring systems

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

A Convergent Synthesis of (±)-Eldanolide Based on Reaction of Aldehyde with Dithio-Substituted Crotyllithium Compound

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Sulfur-Stabilized Carbanions: Electrophilic Reactions of an Allylic Anion Containing Propanedithio and Phenylthio Substituents

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Pyrrolizidine alkaloids. XX. Nemorensine, an alkaloid from Senecio nemorensis L.

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Oxidative cyclization based on reversing the polarity of enol ethers and ketene dithioacetals. Construction of a tetrahydrofuran ring and application to the synthesis of (+)-nemorensic Acid

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

XESTOQUINONE. A NOVEL CARDIOTONIC MARINE NATURAL PRODUCT ISOLATED FROM THE OKINAWAN SEA SPONGEXESTOSPONGIA SAPRA

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Isolation of an Anabolic, Uterotrophic Compound from Corn infected with Gibberella zeae

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

The chemistry of azadirachtin

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Chelation, activation, and proximity effects in the deprotection of dithianes with ZnBr(2): applications in the polyketide field

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Synthetic studies of the HIV-1 protease inhibitive didemnaketals: stereocontrolled synthetic approach to the key mother spiroketals

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Didemnaketals A and B, HIV-1 protease inhibitors from the ascidian Didemnum sp

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

A Reinvestigation of the Didemnaketals from the Palauan AscidianDidemnumsp

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Inhibition of UDP-Gal Mutase and Mycobacterial Galactan Biosynthesis by Pyrrolidine Analogues of Galactofuranose

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Antiprotozoal Activity and Cytotoxicity of Novel 1,7-Dioxadispiro[5.1.5.2]pentadeca-9,12-dien-11-one Derivatives fromAmomum aculeatum

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Minor cytotoxic and antibacterial compounds from the rhizomes of Amomum aculeatum

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Synthesis of (+/-)-aculeatins A and B.

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Mucocin: A New Annonaceous Acetogenin Bearing a Tetrahydropyran Ring

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Stereoselective total synthesis of mucocin, an antitumor agent

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Development of β-keto 1,3-dithianes as versatile intermediates for organic synthesis

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021

Reaction of 1,3-dithienium fluoroborate with 1,3-dienes. Synthesis of .DELTA.3-cyclopenten-1-ones

1 reference

https://api.crossref.org/works/10.1016%2FS0040-4020%2803%2900955-4

7 January 2021