(Q42132537)

17 October 2017

Enantioselective organo-SOMO cascade cycloadditions: a rapid approach to molecular complexity from simple aldehydes and olefins (English)

1 reference

17 October 2017

1 reference

1 reference

3

David W C MacMillan

1 reference

17 October 2017

Nathan T Jui

1

1 reference

17 October 2017

Esther C Y Lee

series ordinal

2

1 reference

17 October 2017

language of work or name

English

0 references

publication date

1 July 2010

1 reference

Journal of the American Chemical Society

17 October 2017

1 reference

17 October 2017

132

1 reference

17 October 2017

29

1 reference

17 October 2017

10015-10017

1 reference

The Diels--Alder reaction in total synthesis.

17 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3041020

Catalytic enantioselective Diels--Alder reactions: methods, mechanistic fundamentals, pathways, and applications

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3041020

Enantioselective organo-singly occupied molecular orbital catalysis: the carbo-oxidation of styrenes

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3041020

Enantioselective organocatalytic singly occupied molecular orbital activation: the enantioselective alpha-enolation of aldehydes

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3041020

Carborane acids. New "strong yet gentle" acids for organic and inorganic chemistry

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3041020

Chemical Redox Agents for Organometallic Chemistry

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3041020

Enantioselective alpha-arylation of aldehydes via organo-SOMO catalysis. An ortho-selective arylation reaction based on an open-shell pathway

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3041020

Enantioselective intramolecular Friedel-Crafts-type alpha-arylation of aldehydes.

17 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3041020

Enantioselective organo-SOMO catalysis: the alpha-vinylation of aldehydes

17 August 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20593858

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Enantioselective organocatalysis using SOMO activation

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20593858

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Synthesen in der hydroaromatischen Reihe

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JA104313X

The Stereochemistry of the Ivanov and Reformatsky Reactions. I

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JA104313X

Identifiers

DOI

10.1021/JA104313X

1 reference

17 October 2017

1 reference

17 October 2017

PubMed publication ID

20593858

1 reference