Concise total syntheses of palominol, dolabellatrienone, beta-araneosene, and isoedunol via an enantioselective Diels-Alder macrobicyclization (Q82282356)

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scientific article published on 01 January 2006

Language	Label	Description	Also known as
English	Concise total syntheses of palominol, dolabellatrienone, beta-araneosene, and isoedunol via an enantioselective Diels-Alder macrobicyclization	scientific article published on 01 January 2006

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scholarly article

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Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16417362%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

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

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16417362%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

enantioselectivity

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based on heuristic

inferred from title

language of work or name

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Journal of the American Chemical Society

publication date

1 January 2006

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16417362%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

Journal of the American Chemical Society

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16417362%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

128

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16417362%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

3

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Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16417362%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

740-742

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Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16417362%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

Modulation of the reactivity profile of IBX by ligand complexation: ambient temperature dehydrogenation of aldehydes and ketones to alpha,beta-unsaturated carbonyl compounds

1 reference

11 October 2022

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Enantioselective organocatalytic intramolecular Diels-Alder reactions. The asymmetric synthesis of solanapyrone D.

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JA0576379

An Enantioselective Synthesis of FR182877 Provides a Chemical Rationalization of Its Structure and Affords Multigram Quantities of Its Direct Precursor

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JA0576379

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/JA0576379

Preparation of an optically active prostaglandin intermediate via asymmetric induction

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JA0576379

Structures and reactivities of new dolabellane diterpenoids from the Caribbean gorgonian Eunicea laciniata

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JA0576379

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

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JA0576379

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/JA0576379

Oxidation of silyl enol ethers by using IBX and IBX.N-oxide complexes: a mild and selective reaction for the synthesis of enones

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JA0576379

New bicyclic diterpenoids from the Caribbean gorgonian octocoral Eunicea calyculata

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JA0576379

Enantioselective total synthesis of isoedunol and beta-araneosene featuring unconventional strategy and methodology

1 reference

11 October 2022

https://opencitations.net/index/coci/api/v1/references/10.1021/JA0576379

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/JA0576379

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/JA0576379

Identifiers

10.1021/JA0576379

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16417362%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16417362%20AND%20SRC:MED&resulttype=core&format=json

15 January 2020

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