Enantioselective total syntheses of (-)-palau'amine, (-)-axinellamines, and (-)-massadines (Q38433980)

3 September 2017

Enantioselective total syntheses of (-)-palau'amine, (-)-axinellamines, and (-)-massadines (English)

1 reference

3 September 2017

1 reference

Ian B Seiple

1

1 reference

3 September 2017

Shun Su

2

1 reference

3 September 2017

Ian S Young

3

1 reference

3 September 2017

Akifumi Nakamura

4

1 reference

3 September 2017

Junichiro Yamaguchi

5

1 reference

3 September 2017

Lars Jørgensen

6

1 reference

3 September 2017

Rodrigo A Rodriguez

7

1 reference

3 September 2017

Daniel P O'Malley

8

1 reference

3 September 2017

Tanja Gaich

9

1 reference

3 September 2017

Matthias Köck

10

1 reference

3 September 2017

Phil S Baran

11

1 reference

3 September 2017

language of work or name

English

0 references

publication date

23 August 2011

1 reference

Journal of the American Chemical Society

3 September 2017

1 reference

3 September 2017

133

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3 September 2017

37

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3 September 2017

14710-14726

1 reference

Protecting-group-free synthesis as an opportunity for invention

3 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173569

Practical C-H functionalization of quinones with boronic acids

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173569

Synthetic Studies on Palau'amine. Construction of the Cyclopentane Core via an Asymmetric 1,3-Dipolar Cycloaddition

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173569

Revisiting the Kinnel-Scheuer hypothesis for the biosynthesis of palau'amine

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173569

Bromopyrrole alkaloids as lead compounds against protozoan parasites

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173569

Sceptrin, a marine natural compound, inhibits cell motility in a variety of cancer cell lines

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173569

Toward palau'amine: Hg(OTf)2-catalyzed synthesis of the cyclopentane core.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173569

Enantiospecific Total Syntheses of Kapakahines B and F

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173569

EVALUATION OF STRATEGIES FOR THE SYNTHESIS OF THE GUANIDINE HEMIAMINAL PORTION OF PALAU'AMINE.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173569

Identification of the binding of sceptrin to MreB via a bidirectional affinity protocol.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173569

On the structure of palau'amine: evidence for the revised relative configuration from chemical synthesis

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173569

Reaction mechanism and kinetics of the traceless Staudinger ligation

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173569

Short total synthesis of (+/-)-sceptrin.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173569

Triflimide activation of a chiral oxazaborolidine leads to a more general catalytic system for enantioselective Diels-Alder addition.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173569

Marine natural products as prototype agrochemical agents.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173569

Axinellamines A-D, Novel Imidazo-Azolo-Imidazole Alkaloids from the Australian Marine Sponge Axinella sp.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173569

Total syntheses of the Securinega alkaloids (+)-14,15-dihydronorsecurinine, (-)-norsecurinine, and phyllanthine

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173569

Staudinger ligation: a peptide from a thioester and azide.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173569

Determination of the complete three-dimensional structure of the trypsin inhibitor from squash seeds in aqueous solution by nuclear magnetic resonance and a combination of distance geometry and dynamical simulated annealing

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173569

Molecular dynamics simulation techniques for determination of molecular structures from nuclear magnetic resonance data

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173569

Protein structures from NMR.

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173569

Aiming for the ideal synthesis

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173569

Exploring symmetry-based logic for a synthesis of palau'amine

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173569

Facile synthesis of the trans-fused azabicyclo[3.3.0]octane core of the palau'amines and the tricyclic core of the axinellamines from a common intermediate

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173569

Direct C−H Arylation of Electron-Deficient Heterocycles with Arylboronic Acids

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173569

Total synthesis of palau'amine

23 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173569

Total syntheses of (+/-)-massadine and massadine chloride

23 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173569

A "traceless" Staudinger ligation for the chemoselective synthesis of amide bonds

23 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173569

Anti-muscarinic activity of a family of C11N5 compounds isolated from Agelas sponges

23 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173569

Rational design of highly effective asymmetric Diels-Alder catalysts bearing 4,4'-sulfonamidomethyl groups

23 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173569

Studies toward the total synthesis of the oroidin dimers.

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173569

A synthesis of Tamiflu by using a barium-catalyzed asymmetric Diels-Alder-type reaction.

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173569

Synthetic access to the chlorocyclopentane cores of the proposed original and revised structures of palau'amine

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173569

Sceptrin as a potential biosynthetic precursor to complex pyrrole-imidazole alkaloids: the total synthesis of ageliferin

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173569

Density functional theory guided design of exo-selective dehydroalanine dienophiles for application toward the synthesis of palau'amine

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173569

Antifouling activity of bromotyrosine-derived sponge metabolites and synthetic analogues.

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173569

Oxidation of secondary amines catalyzed by dirhodium caprolactamate.

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173569

Mechanism of the vinylcyclobutane rearrangement of sceptrin to ageliferin and nagelamide E.

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173569

Short, enantioselective total synthesis of sceptrin and ageliferin by programmed oxaquadricyclane fragmentation

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173569

Synthesis of 3'-deoxy-3'-difluoromethyl azanucleosides from trans-4-hydroxy-l-proline

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173569

Brominated pyrrole alkaloids from marine Agelas sponges reduce depolarization-induced cellular calcium elevation

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173569

o-Iodoxybenzoic acid (IBX) as a viable reagent in the manipulation of nitrogen- and sulfur-containing substrates: scope, generality, and mechanism of IBX-mediated amine oxidations and dithiane deprotections

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173569

Enantioselective total synthesis of (+)-dibromophakellstatin

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173569

Stereocontrolled synthesis of triazacyclopenta[cd]pentalenes by intramolecular 1,3-dipolar cycloaddition reactions of azomethine imines.

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173569

A study on the mechanism of action of sceptrin, an antimicrobial agent isolated from the South Pacific sponge Agelas mauritiana.

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173569

Total synthesis of marine natural products without using protecting groups

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173569

Catalytic CC, CN, and CO Ullmann-Type Coupling Reactions

31 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3173569

New bromopyrrole alkaloids from the Indopacific sponge Agelas nakamurai

1 October 2018

1 reference

12 December 2020

Synthesis of slagenins A, B, and C

1 reference

12 December 2020

Enantioselective strategy to the spirocyclic core of Palau'amine and related bisguanidine marine alkaloids

1 reference

12 December 2020

High-Yielding Staudinger Ligation of a Phosphinothioester and Azide To Form a Peptide

1 reference

12 December 2020

Synthesis of Mauritiamine

1 reference

12 December 2020

Bromosceptrin, an alkaloid from the marine sponge Agelas conifera

1 reference

12 December 2020

Synthesis of axinohydantoins

1 reference

12 December 2020

Staudinger Ligation of α-Azido Acids Retains Stereochemistry

1 reference

12 December 2020

Highly diastereoselective desymmetrizations of cyclo(Pro,Pro): an enantioselective strategy toward phakellstatin and phakellin

1 reference

12 December 2020

Massadine, a novel geranylgeranyltransferase type I inhibitor from the marine sponge Stylissa aff. massa

1 reference

12 December 2020

Intramolecular Staudinger ligation: a powerful ring-closure method to form medium-sized lactams

1 reference

12 December 2020

Spirocycloisomerization of tethered alkylidene glycocyamidines: synthesis of a base template common to the palau'amine family of alkaloids

1 reference

12 December 2020

Highly regioselective Diels-Alder reactions toward oroidin alkaloids: use of a tosylvinyl moiety as a nitrogen masking group with adjustable electronics

1 reference

12 December 2020

Regiocontrol in MnIII-Mediated Oxidative Heterobicyclizations: Access to the Core Skeletons of Oroidin Dimers

1 reference

12 December 2020

Stylissadines A and B: the first tetrameric pyrrole-imidazole alkaloids

1 reference

12 December 2020

Chiral oxazaborolidine-aluminum bromide complexes are unusually powerful and effective catalysts for enantioselective Diels-Alder reactions

1 reference

12 December 2020

Natural Products, Stylissadines A and B, Specific Antagonists of the P2X7Receptor, an Important Inflammatory Target1

1 reference

12 December 2020

Structural assignment of tetrabromostyloguanidine: does the relative configuration of the palau'amines need revision?

1 reference

12 December 2020

A Diels-Alder approach to (-)-ovalicin

1 reference

12 December 2020

Total synthesis of dimeric pyrrole-imidazole alkaloids: sceptrin, ageliferin, nagelamide e, oxysceptrin, nakamuric acid, and the axinellamine carbon skeleton

1 reference

12 December 2020

Enantioselective total synthesis of cyathin A3

1 reference

12 December 2020

Massadine chloride: a biosynthetic precursor of massadine and stylissadine

1 reference

12 December 2020

The pursuit of palau'amine

1 reference

12 December 2020

Studies toward the total synthesis of axinellamine and massadine

1 reference

12 December 2020

Enantioselective synthesis of (+)-monobromophakellin and (+)-phakellin: a concise phakellin annulation strategy applicable to Palau'amine

1 reference

12 December 2020

Synthesis of 1,9-dideoxy-pre-axinellamine

1 reference

12 December 2020

Total synthesis of (+/-)-axinellamines A and B

1 reference

12 December 2020

Enantioselective Synthesis of the Carbocyclic D-Ring Subunit of Massadine

1 reference

12 December 2020

Stable 5-substituted cyclopentadienes for the Diels-Alder cycloaddition and their application to the synthesis of palau'amine

1 reference

12 December 2020

Ugi-4-Component Reaction Enabling Rapid Access to the Core Fragment of Massadine

1 reference

12 December 2020

Extending Pummerer reaction chemistry: studies in the palau'amine synthesis area

1 reference

12 December 2020

Transition Metal Catalyzed Synthesis of Arylamines and Aryl Ethers from Aryl Halides and Triflates: Scope and Mechanism

1 reference

12 December 2020

Determining stereo-specific 1H nuclear magnetic resonance assignments from distance geometry calculations

1 reference

12 December 2020

Axinellamines A and B, New Pyrrole Alkaloids of the Marine Sponge Axinella Sp.

1 reference

12 April 2024

https://opencitations.net/index/api/v1/citations/10.3987/COM-98-8142

Identifiers

DOI

10.1021/JA2047232

1 reference

release_mtegthqwfzdelbwwqymwnhgubq

3 September 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/mtegthqwfzdelbwwqymwnhgubq

24 November 2022

mapped directly with Wikidata item

1 reference

3 September 2017

PubMed publication ID

21861522

1 reference