(Q42631146)

4 November 2017

Rate limiting step precedes C-C bond formation in the archetypical proline-catalyzed intramolecular aldol reaction (English)

1 reference

4 November 2017

3

K N Houk

1 reference

4 November 2017

Hui Zhu

1

1 reference

4 November 2017

Fernando R Clemente

series ordinal

2

1 reference

4 November 2017

Matthew P Meyer

series ordinal

4

1 reference

4 November 2017

language of work or name

English

0 references

publication date

1 February 2009

1 reference

Journal of the American Chemical Society

4 November 2017

1 reference

4 November 2017

131

1 reference

4 November 2017

1632-1633

1 reference

4 November 2017

5

1 reference

Asymmetric enamine catalysis

4 November 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3044651

Asymmetric organocatalysis

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3044651

In the Golden Age of Organocatalysis

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3044651

Enamine-based organocatalysis with proline and diamines: the development of direct catalytic asymmetric Aldol, Mannich, Michael, and Diels-alder reactions

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3044651

Asymmetric Catalysis Special Feature Part II: New mechanistic studies on the proline-catalyzed aldol reaction

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3044651

Kinetic and Stereochemical Evidence for the Involvement of Only One Proline Molecule in the Transition States of Proline-Catalyzed Intra- and Intermolecular Aldol Reactions

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3044651

Development of the Colle-Salvetti correlation-energy formula into a functional of the electron density

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3044651

A mechanistic probe for asymmetric reactions: deuterium isotope effects at enantiotopic groups

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3044651

Quantum mechanical continuum solvation models.

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3044651

Theory of asymmetric organocatalysis of Aldol and related reactions: rationalizations and predictions

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3044651

Quantum mechanical predictions of the stereoselectivities of proline-catalyzed asymmetric intermolecular aldol reactions

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3044651

Chemistry. The simplest "enzyme".

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3044651

The origin of stereoselectivity in proline-catalyzed intramolecular aldol reactions

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3044651

Transition states of amine-catalyzed aldol reactions involving enamine intermediates: theoretical studies of mechanism, reactivity, and stereoselectivity

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3044651

Catalytic asymmetric conjugate addition of nitroalkanes to cycloalkenones

16 August 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19191687

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

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

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19191687

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1021/JA806672Y

1 reference

4 November 2017

1 reference

4 November 2017

1 reference