Highly enantioselective organocatalytic formation of a quaternary carbon center via chiral Brønsted acid catalyzed self-coupling of enamides

Christine Baudequin; Alexandru Zamfir; Svetlana Tsogoeva

doi:10.1039/B804477E

Journal Articles Chemical Communications Year : 2008

Highly enantioselective organocatalytic formation of a quaternary carbon center via chiral Brønsted acid catalyzed self-coupling of enamides

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Christine Baudequin

Function : Author
PersonId : 184145
IdHAL : christine-baudequin
ORCID : 0000-0002-7390-9042
IdRef : 09023801X

Chimie Organique et Bioorganique : Réactivité et Analyse

Alexandru Zamfir

Function : Author

Friedrich-Alexander Universität Erlangen-Nürnberg

Svetlana Tsogoeva

Function : Author

Friedrich-Alexander Universität Erlangen-Nürnberg

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Chemical Sciences Catalysis Chemical Sciences Organic chemistry

Christine Baudequin : Connect in order to contact the contributor

https://hal-normandie-univ.archives-ouvertes.fr/hal-02385370

Submitted on : Thursday, November 28, 2019-5:31:19 PM

Last modification on : Saturday, June 25, 2022-9:54:48 AM

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hal-02385370 , version 1 (28-11-2019)

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HAL Id : hal-02385370 , version 1
DOI : 10.1039/B804477E

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Christine Baudequin, Alexandru Zamfir, Svetlana Tsogoeva. Highly enantioselective organocatalytic formation of a quaternary carbon center via chiral Brønsted acid catalyzed self-coupling of enamides. Chemical Communications, 2008, 38, pp.4637-4639. ⟨10.1039/B804477E⟩. ⟨hal-02385370⟩

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Highly enantioselective organocatalytic formation of a quaternary carbon center via chiral Brønsted acid catalyzed self-coupling of enamides

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