(Q33989232)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20550127%20AND%20SRC:MED&resulttype=core&format=json

5 February 2020

title

An enantioselective Claisen rearrangement catalyzed by N-heterocyclic carbenes (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20550127%20AND%20SRC:MED&resulttype=core&format=json

5 February 2020

1 reference

Jessada Mahatthananchai

series ordinal

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20550127%20AND%20SRC:MED&resulttype=core&format=json

5 February 2020

Juthanat Kaeobamrung

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20550127%20AND%20SRC:MED&resulttype=core&format=json

5 February 2020

Pinguan Zheng

series ordinal

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20550127%20AND%20SRC:MED&resulttype=core&format=json

5 February 2020

Jeffrey W Bode

series ordinal

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20550127%20AND%20SRC:MED&resulttype=core&format=json

5 February 2020

language of work or name

English

0 references

publication date

1 July 2010

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20550127%20AND%20SRC:MED&resulttype=core&format=json

Journal of the American Chemical Society

5 February 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20550127%20AND%20SRC:MED&resulttype=core&format=json

5 February 2020

volume

132

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20550127%20AND%20SRC:MED&resulttype=core&format=json

5 February 2020

issue

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20550127%20AND%20SRC:MED&resulttype=core&format=json

5 February 2020

page(s)

8810-8812

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20550127%20AND%20SRC:MED&resulttype=core&format=json

Enantioselective Claisen rearrangements with a hydrogen-bond donor catalyst

5 February 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2902991

Observation of an acryloyl-thiamin diphosphate adduct in the first step of clavulanic acid biosynthesis.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2902991

N-heterocyclic carbene-catalyzed generation of alpha,beta-unsaturated acyl imidazoliums: synthesis of dihydropyranones by their reaction with enolates

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2902991

Stereodivergency of triazolium and imidazolium-derived NHCs for catalytic, enantioselective cyclopentane synthesis

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2902991

Catalytic enantioselective Meerwein-Eschenmoser Claisen rearrangement: asymmetric synthesis of allyl oxindoles

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2902991

Biomimetic carbene-catalyzed oxidations of aldehydes using TEMPO.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2902991

Enantioselective, NHC-catalyzed bicyclo-beta-lactam formation via direct annulations of enals and unsaturated N-sulfonyl ketimines

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2902991

N-heterocyclic carbene-catalyzed redox amidations of alpha-functionalized aldehydes with amines

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2902991

Nucleophilic carbene and HOAt relay catalysis in an amide bond coupling: an orthogonal peptide bond forming reaction

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2902991

Enantioselective, cyclopentene-forming annulations via NHC-catalyzed benzoin-oxy-cope reactions

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2902991

Lewis acid-Lewis acid heterobimetallic cooperative catalysis: mechanistic studies and application in enantioselective aza-Michael reaction

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2902991

Imidazolinium salts as catalysts for the aza-Diels-Alder reaction

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2902991

Catalytic generation of activated carboxylates: direct, stereoselective synthesis of beta-hydroxyesters from epoxyaldehydes.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2902991

Kinetics of the thiazolium ion-catalyzed benzoin condensation

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2902991

Enantioselective Claisen rearrangements: development of a first generation asymmetric acyl-Claisen reaction

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2902991

Tandem oxidation of allylic and benzylic alcohols to esters catalyzed by N-heterocyclic carbenes

29 October 2018

1 reference

12 December 2020

NHC catalyzed oxidations of aldehydes to esters: chemoselective acylation of alcohols in presence of amines

1 reference

12 December 2020

Modular synthesis of candidate indole-based insulin mimics by Claisen rearrangement

1 reference

12 December 2020

N-heterocyclic carbene-catalyzed amidation of unactivated esters with amino alcohols

1 reference

12 December 2020

Organocatalytic asymmetric 5-hydroxyisoxazolidine synthesis: a highly enantioselective route to beta-amino acids

1 reference

12 December 2020

Function-oriented synthesis: studies aimed at the synthesis and mode of action of 1alpha-alkyldaphnane analogues

1 reference

12 December 2020

Synthesis of an N-mesityl substituted chiral imidazolium salt for NHC-catalyzed reactions

1 reference

12 December 2020

The Catalytic Enantioselective Claisen Rearrangement of an Allyl Vinyl Ether This work was financially supported by the Deutsche Forschungsgemeinschaft, the Fonds der Chemischen Industrie, and the Dr. Otto Röhm Gedächtnisstiftung. M.H. thanks Prof.

1 reference

12 December 2020

Stereoselective synthesis of (E)-alpha,beta-unsaturated esters via carbene-catalyzed redox esterification

1 reference

12 December 2020

Unexpected steric effects of "remote" alkyl groups on the rate of conjugate additions to alkyl alpha,beta-ethylenic sulfones, sulfoxides, and esters

1 reference

12 December 2020

Conversion of alpha-haloaldehydes into acylating agents by an internal redox reaction catalyzed by nucleophilic carbenes

1 reference

12 December 2020

Catalytic generation of activated carboxylates from enals: a product-determining role for the base

1 reference

12 December 2020

Identifiers

DOI

10.1021/JA103631U

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20550127%20AND%20SRC:MED&resulttype=core&format=json

5 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20550127%20AND%20SRC:MED&resulttype=core&format=json

5 February 2020

PubMed publication ID

20550127

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20550127%20AND%20SRC:MED&resulttype=core&format=json