Lessons Learned while Traversing the Welwitindolinone Alkaloids Obstacle Course (Q36212300)

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12 February 2020

title

Lessons Learned while Traversing the Welwitindolinone Alkaloids Obstacle Course (English)

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12 February 2020

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2

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author name string

Vikram Bhat

series ordinal

1

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Viresh H Rawal

series ordinal

3

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publication date

24 September 2011

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12 February 2020

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volume

67

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issue

52

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page(s)

100997-110104

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

12 February 2020

cites work

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

1 October 2017

1 reference

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Total synthesis of N-methylwelwitindolinone D isonitrile

1 October 2017

1 reference

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Palladium-catalyzed conversion of aryl and vinyl triflates to bromides and chlorides

1 October 2017

1 reference

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

1 October 2017

1 reference

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

1 October 2017

1 reference

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

1 October 2017

1 reference

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

1 October 2017

1 reference

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An approach to the total synthesis of welwistatin

1 October 2017

1 reference

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pi-Allylpalladium-Mediated Catalytic Synthesis of Functionalized Allenes This work was supported by the "Research for the Future" Program, the Japan Society for the Promotion of Science, and a Grant-in-Aid for Scientific Research from the Ministry o

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3434954

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

1 October 2017

1 reference

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

29 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3434954

Ruthenium-catalyzed transformation of alkenyl triflates to alkenyl halides

22 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3434954

Access to a welwitindolinone core using sequential cycloadditions

22 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3434954

Bridgehead enolates and bridgehead alkenes in a welwistatin model series

22 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3434954

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

22 September 2018

1 reference

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

22 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3434954

Total synthesis of (+/-)-welwitindolinone a isonitrile

22 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3434954

Enantioselective total syntheses of welwitindolinone A and fischerindoles I and G.

22 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3434954

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

22 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3434954

Reverse aromatic cope rearrangement of 2-allyl-3-alkylideneindolines driven by olefination of 2-allylindolin-3-ones: synthesis of alpha-allyl-3-indole acetate derivatives

22 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3434954

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

22 September 2018

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12 December 2020

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

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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

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

1 reference

12 December 2020

Oxidized welwitindolinones from terrestrial fischerella spp

1 reference

12 December 2020

A mild and efficient synthesis of oxindoles: progress towards the synthesis of welwitindolinone A isonitrile

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12 December 2020

An Expedient Construction of Seven-Membered Rings Adjoining Aromatic Systems

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12 December 2020

10.1016/J.TET.2011.09.088

Identifiers

DOI

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12 February 2020

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12 February 2020

PubMed publication ID

22962500

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22962500%20AND%20SRC:MED&resulttype=core&format=json