(Q79758502)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16787080%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

title

Enantioselective synthesis of bridged- or fused-ring bicyclic ketones by a catalytic asymmetric Michael addition pathway (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16787080%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

1 reference

3

E J Corey

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16787080%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

author name string

Duan Liu

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16787080%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

Sungwoo Hong

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16787080%20AND%20SRC:MED&resulttype=core&format=json

Journal of the American Chemical Society

25 December 2019

language of work or name

English

1 reference

inferred from

publication date

1 June 2006

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16787080%20AND%20SRC:MED&resulttype=core&format=json

Journal of the American Chemical Society

25 December 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16787080%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

volume

128

1 reference

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25 December 2019

issue

25

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16787080%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

page(s)

8160-8161

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16787080%20AND%20SRC:MED&resulttype=core&format=json

Enantioselective and structure-selective Diels-Alder reactions of unsymmetrical quinones catalyzed by a chiral oxazaborolidinium cation. Predictive selection rules.

25 December 2019

cites work

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JA063332Y

Triflimide activation of a chiral oxazaborolidine leads to a more general catalytic system for enantioselective Diels-Alder addition.

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JA063332Y

Application of chiral cationic catalysts to several classical syntheses of racemic natural products transforms them into highly enantioselective pathways

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JA063332Y

Broad-spectrum enantioselective diels-alder catalysis by chiral, cationic oxazaborolidines.

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JA063332Y

Concise total syntheses of palominol, dolabellatrienone, beta-araneosene, and isoedunol via an enantioselective Diels-Alder macrobicyclization

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JA063332Y

Asymmetric Diels-Alder reactions catalyzed by a triflic acid activated chiral oxazaborolidine

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JA063332Y

Asymmetric Dearomatization of η2-Arene Complexes: Synthesis of Stereodefined Functionalized Cyclohexenones and Cyclohexenes

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JA063332Y

Enantioselective mukaiyama-michael reactions of 2-carbomethoxy cyclopentenone catalyzed by chiral bis(Oxazoline)-Cu(II) complexes

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JA063332Y

Identifiers

DOI

10.1021/JA063332Y

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16787080%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

1 reference