Formal syntheses of naturally occurring welwitindolinones (Q36154505)

12 August 2017

Formal syntheses of naturally occurring welwitindolinones (English)

1 reference

12 August 2017

Tsung-hao Fu

1

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12 August 2017

William T McElroy

series ordinal

2

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12 August 2017

Mariam Shamszad

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3

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12 August 2017

Stephen F Martin

series ordinal

4

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12 August 2017

language of work or name

English

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publication date

25 July 2012

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12 August 2017

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12 August 2017

14

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12 August 2017

15

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12 August 2017

3834-3837

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Lessons Learned while Traversing the Welwitindolinone Alkaloids Obstacle Course

12 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3416027

Total synthesis of oxidized welwitindolinones and (-)-N-methylwelwitindolinone C isonitrile

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3416027

A unified route to the welwitindolinone alkaloids: total syntheses of (-)-N-methylwelwitindolinone C isothiocyanate, (-)-N-methylwelwitindolinone C isonitrile, and (-)-3-hydroxy-N-methylwelwitindolinone C isothiocyanate

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3416027

Total synthesis of (-)-N-methylwelwitindolinone C isothiocyanate

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3416027

Directed oxidative cyclizations to C2- or C4-positions of indole: efficient construction of the bicyclo[4.3.1]decane core of welwitindolinones.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3416027

Total synthesis of N-methylwelwitindolinone D isonitrile

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3416027

Approaches to N-methylwelwitindolinone C isothiocyanate: facile synthesis of the tetracyclic core

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3416027

Synthesis of β-Heteroaryl Propionates via Trapping of Carbocations with π-Nucleophiles

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3416027

Synthesis of the bicyclic welwitindolinone core via an alkylation/cyclization cascade reaction

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3416027

Enantiospecific total synthesis of the hapalindoles, fischerindoles, and welwitindolinones via a redox economic approach

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3416027

Welwistatin support studies: expansion and limitation of aryllead(IV) coupling reactions

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3416027

An approach to the total synthesis of welwistatin

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3416027

Evolution of the vinylogous Mannich reaction as a key construction for alkaloid synthesis

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3416027

Microtubule effects of welwistatin, a cyanobacterial indolinone that circumvents multiple drug resistance

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3416027

Welwitindolinone analogues that reverse P-glycoprotein-mediated multiple drug resistance.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3416027

Welwitindolinone C synthetic studies. Construction of the welwitindolinone carbon skeleton via a transannular nitrone cycloaddition

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3416027

Asymmetric Transition Metal-Catalyzed Allylic Alkylations

2 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3416027

Total syntheses of the elusive welwitindolinones with bicyclo[4.3.1] cores

2 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3416027

Concise and very efficient synthesis of the N-methylwelwistatin tetracyclic core based on an anionic domino process

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3416027

Access to a welwitindolinone core using sequential cycloadditions

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3416027

Bridgehead enolates and bridgehead alkenes in a welwistatin model series

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3416027

First catalytic and green synthesis of aryl-(Z)-vinyl chlorides and its plausible addition-elimination mechanism.

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3416027

A mild synthesis of vinyl halides and gem-dihalides using triphenyl phosphite-halogen-based reagents.

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3416027

Aryllead(IV) reagents in synthesis: formation of the C11 quaternary center of N-methylwelwitindolinone C isothiocyanate.

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3416027

Rapid access to the Welwitindolinone alkaloid skeleton by cyclization of indolecarboxaldehyde substituted cyclohexanones

23 September 2018

1 reference

12 December 2020

Stereocontrolled synthesis of 20,21-dihydro N-methylwelwitindolinone B isothiocyanate

1 reference

12 December 2020

STUDIES ON STEROIDAL COMPOUNDS. X. PREPARATION OF 17BETA-CHLORO STEROIDS

1 reference

12 December 2020

A synthesis of the welwistatin core

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12 December 2020

Rapid synthesis of the N-methylwelwitindolinone skeleton

1 reference

12 December 2020

Synthetic studies on quinine: quinuclidine construction via a ketone enolate regio- and diastereoselective Pd-mediated allylic alkylation

1 reference

12 December 2020

Concise synthesis of the bicyclic scaffold of N-methylwelwitindolinone C isothiocyanate via an indolyne cyclization

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12 December 2020

Total synthesis: Welwitindolinone is well worth it

1 reference

12 December 2020

Practical and robust method for regio- and stereoselective preparation of (E)-ketene tert-butyl TMS acetals and beta-ketoester-derived tert-butyl (1Z,3E)-1,3-bis(TMS)dienol ethers

1 reference

12 December 2020

Oxidized welwitindolinones from terrestrial fischerella spp

1 reference

12 December 2020

Metal-catalyzed enantioselective allylation in asymmetric synthesis

1 reference

12 December 2020

Easily Prepared Air- and Moisture-Stable Pd–NHC (NHC=N-Heterocyclic Carbene) Complexes: A Reliable, User-Friendly, Highly Active Palladium Precatalyst for the Suzuki–Miyaura Reaction

1 reference

12 December 2020

Identifiers

DOI

10.1021/OL301424H

1 reference

12 August 2017

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12 August 2017

PubMed publication ID

22830424

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