(Q41787537)

English

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

scientific article published on January 2009

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

9 October 2017

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

1 reference

Europe PubMed Central

PMC publication ID

9 October 2017

natural product

1 reference

based on heuristic

inferred from title

David MacMillan

3

object named as

David W C MacMillan

1 reference

Europe PubMed Central

PMC publication ID

9 October 2017

author name string

Bryon Simmons

1

1 reference

Europe PubMed Central

PMC publication ID

9 October 2017

Abbas M Walji

2

1 reference

Europe PubMed Central

PMC publication ID

9 October 2017

language of work or name

0 references

publication date

1 January 2009

1 reference

Europe PubMed Central

PMC publication ID

9 October 2017

Angewandte Chemie International Edition

0 references

48

1 reference

Europe PubMed Central

PMC publication ID

9 October 2017

24

1 reference

Europe PubMed Central

PMC publication ID

9 October 2017

4349-4353

1 reference

Europe PubMed Central

PMC publication ID

9 October 2017

Hydroamination: direct addition of amines to alkenes and alkynes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3057093

6 June 2018

Asymmetric enamine catalysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3057093

6 June 2018

Asymmetric Organocatalytic Domino Reactions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3057093

6 June 2018

A highly enantioselective Brønsted acid catalyzed cascade reaction: organocatalytic transfer hydrogenation of quinolines and their application in the synthesis of alkaloids

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3057093

6 June 2018

Catalytic asymmetric tandem transformations triggered by conjugate additions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3057093

6 June 2018

Asymmetric multicomponent domino reactions and highly enantioselective conjugated addition of thiols to alpha,beta-unsaturated aldehydes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3057093

6 June 2018

Enantioselective organo-cascade catalysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3057093

6 June 2018

Direct and enantioselective organocatalytic alpha-chlorination of aldehydes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3057093

6 June 2018

A Facile and Rapid Route to Highly Enantiopure 1,2‐Diols by Novel Catalytic Asymmetric α‐Aminoxylation of Aldehydes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3057093

6 June 2018

The direct and enantioselective organocatalytic alpha-oxidation of aldehydes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3057093

6 June 2018

Organocatalytic asymmetric synthesis of alpha,alpha-disubstituted alpha-amino acids and derivatives

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3057093

18 August 2018

One-pot multi-component asymmetric cascade reactions catalyzed by soluble star polymers with highly branched non-interpenetrating catalytic cores.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3057093

18 August 2018

A powerful chiral counterion strategy for asymmetric transition metal catalysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3057093

18 August 2018

Enantioselective organocatalytic amine conjugate addition

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3057093

18 August 2018

The importance of iminium geometry control in enamine catalysis: identification of a new catalyst architecture for aldehyde-aldehyde couplings

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3057093

18 August 2018

The first enantioselective organocatalytic Mukaiyama-Michael reaction: a direct method for the synthesis of enantioenriched gamma-butenolide architecture

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3057093

18 August 2018

Direct L-proline-catalyzed asymmetric alpha-amination of ketones.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3057093

18 August 2018

Direct catalytic asymmetric alpha-amination of aldehydes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3057093

18 August 2018

A highly enantioselective amino acid-catalyzed route to functionalized alpha-amino acids

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3057093

18 August 2018

Enantioselective organocatalytic indole alkylations. Design of a new and highly effective chiral amine for iminium catalysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3057093

18 August 2018

The constituents of the root and stem of Aristolochia heterophylla Hemsl

1 reference

https://pubmed.ncbi.nlm.nih.gov/19434637

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Organocatalysed asymmetric beta-amination and multicomponent syn-selective diamination of alpha,beta-unsaturated aldehydes

1 reference

https://pubmed.ncbi.nlm.nih.gov/19434637

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Catalytic asymmetric diamination of conjugated dienes and triene

1 reference

https://pubmed.ncbi.nlm.nih.gov/19434637

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enamine catalysis is a powerful strategy for the catalytic generation and use of carbanion equivalents

1 reference

https://pubmed.ncbi.nlm.nih.gov/19434637

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Organocatalytic enantioselective aminosulfenylation of alpha,beta-unsaturated aldehydes

1 reference

https://pubmed.ncbi.nlm.nih.gov/19434637

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Sharpless Asymmetric Aminohydroxylation -Scope and Limitation

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1002/ANIE.200900220

Identifiers

10.1002/ANIE.200900220

1 reference

Europe PubMed Central

PMC publication ID

9 October 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

9 October 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

9 October 2017

ResearchGate publication ID

0 references

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