Collective synthesis of natural products by means of organocascade catalysis (Q34200273)

31 July 2017

title

Collective synthesis of natural products by means of organocascade catalysis (English)

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31 July 2017

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ChEBI release 2020-05-28

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ChEBI release 2020-05-28

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4

David W C MacMillan

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31 July 2017

Spencer B Jones

1

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31 July 2017

Bryon Simmons

series ordinal

2

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31 July 2017

Anthony Mastracchio

series ordinal

3

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31 July 2017

language of work or name

English

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publication date

13 July 2011

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31 July 2017

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31 July 2017

volume

475

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31 July 2017

issue

7355

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31 July 2017

page(s)

183-188

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Organocatalytic cascade reactions as a new tool in total synthesis

31 July 2017

cites work

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3439143

Total synthesis and evaluation of a key series of C5-substituted vinblastine derivatives

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3439143

Concise total syntheses of (+/-)-strychnine and (+/-)-akuammicine.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3439143

Nine-step enantioselective total synthesis of (+)-minfiensine

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3439143

Cycle-specific organocascade catalysis: application to olefin hydroamination, hydro-oxidation, and amino-oxidation, and to natural product synthesis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3439143

Enantioselective organo-cascade catalysis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3439143

Total synthesis of (+)-aspidospermidine: a new strategy for the enantiospecific synthesis of aspidosperma alkaloids

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3439143

5 July 2018

Synthesis of Strychnine.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3439143

Synthesis applications of cationic aza-Cope rearrangements. 26. Enantioselective total synthesis of (-)-strychnine

5 July 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE10232

A novel and general synthetic pathway to strychnos indole alkaloids: total syntheses of (-)-tubifoline, (-)-dehydrotubifoline, and (-)-strychnine using palladium-catalyzed asymmetric allylic substitution

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE10232

A synthesis of strychnine by a longest linear sequence of six steps

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE10232

An efficient approach to Aspidosperma alkaloids via [4 + 2] cycloadditions of aminosiloxydienes: stereocontrolled total synthesis of (+/-)-tabersonine. Gram-scale catalytic asymmetric syntheses of (+)-tabersonine and (+)-16-methoxytabersonine. Asymm

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE10232

Nitrogen heterocycles by palladium-catalyzed cyclization of amino-tethered vinyl halides and ketone enolates

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21753848

12 December 2020

inferred from PubMed ID database lookup

Total Synthesis of (-)-Strychnine via the Wieland-Gumlich Aldehyde

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21753848

12 December 2020

inferred from PubMed ID database lookup

The Mizoroki–Heck Reaction

1 reference

https://api.crossref.org/works/10.1038%2FNATURE10232

7 January 2021

inferred from DOI database lookup

Synthesis of (.+-.)-kopsanone and (.+-.)-10,22-dioxokopsane, hetacyclic indole alkaloids

1 reference

https://api.crossref.org/works/10.1038%2FNATURE10232

7 January 2021

inferred from DOI database lookup

Ringschlussreaktionen anPleiocarpa-Alkaloiden

1 reference

https://api.crossref.org/works/10.1038%2FNATURE10232

7 January 2021

inferred from DOI database lookup

Identifiers

DOI

10.1038/NATURE10232

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Dimensions Publication ID

31 July 2017

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31 July 2017

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