(Q37018384)

17 August 2017

Application of the Rh(II) cyclization/cycloaddition cascade for the total synthesis of (+/-)-aspidophytine (English)

1 reference

17 August 2017

1 reference

2

Albert Padwa

1 reference

17 August 2017

José M Mejía-Oneto

1

1 reference

17 August 2017

language of work or name

English

0 references

publication date

1 July 2006

1 reference

17 August 2017

1 reference

17 August 2017

8

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17 August 2017

15

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17 August 2017

3275-3278

1 reference

Total synthesis of (-)- and ent-(+)-vindoline

17 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2604816

Exploiting the palladium[0]-catalysed Ullmann cross-coupling reaction in natural products chemistry: application to a total synthesis of the alkaloid (+/-)-aspidospermidine

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2604816

Enantioselective total synthesis of aspidophytine

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2604816

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2604816

Cycloaddition chemistry of 2-vinyl-substituted indoles and related heteroaromatic systems

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2604816

A new strategy toward indole alkaloids involving an intramolecular cycloaddition/rearrangement cascade

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2604816

Thionation with the reagent combination of phosphorus pentasulfide and hexamethyldisiloxane

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2604816

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

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2604816

A Biomimetic Approach to the Discorhabdin Alkaloids: Total Syntheses of Discorhabdins C and E and Dethiadiscorhabdin D.

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2604816

Total synthesis of (+/-)-aspidospermidine

4 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2604816

Synthesis of the Pentacyclic Skeleton of the Aspidosperma Alkaloids Using Rhodium Carbenoids as Reactive Intermediates

4 September 2018

1 reference

12 December 2020

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

1 reference

12 December 2020

Intramolecular [3 + 2]-cycloaddition reaction of push-pull dipoles across heteroaromatic pi-systems

1 reference

12 December 2020

Cascade Processes of Metallo Carbenoids

1 reference

12 December 2020

Regiocontrol in an intramolecular Schmidt reaction: total synthesis of (+)-aspidospermidine

1 reference

12 December 2020

Tandem radical cyclizations with iodoaryl azides: formal total synthesis of (+/-)-aspidospermidine

1 reference

12 December 2020

Identifiers

DOI

10.1021/OL061137I

1 reference

release_473qgbckhnbt7fnclcgsbjmbna

17 August 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/473qgbckhnbt7fnclcgsbjmbna

24 November 2022

mapped directly with Wikidata item

1 reference

17 August 2017

PubMed publication ID

16836384

1 reference