Ni-catalyzed Enantioselective C–C Bond-Formation via C(sp2)–O Cleavage in Aryl Esters

Author

Cornella, Josep

Jackson, Evan P.

Martin, Ruben

Publication date

2015



Abstract

<p> We report the first enantioselective C<img alt="[BOND]" src="http://onlinelibrarystatic.wiley.com/undisplayable_characters/00f8ff.gif" />C bond formation through C<img alt="[BOND]" src="http://onlinelibrarystatic.wiley.com/undisplayable_characters/00f8ff.gif" />O bond cleavage using aryl ester counterparts. This method is characterized by its wide substrate scope and results in the formation of quaternary stereogenic centers with high yields and asymmetric induction.</p>

Document Type

Article

Language

English

Subject

nickel catalysis; C–O cleavage; C–O electrophiles; Aryl esters

Publisher

Wiley

Version of

Angew. Chem. Int. Ed.

Grant Agreement Number

info:eu-repo/grantAgreement/ERC/FP7/277883

(CTQ2012-34054)

(SEV-2013-0319)

info:eu-repo/grantAgreement/EC/FP7/328381

Related items

ICIQ foundation

the European Research Council

MINECO

Severo Ochoa Excellence Accreditation

European Union

MINECO,ERC

Documents

Enantioselective C-O cleavage aryl esters pdf.pdf

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Rights

© 1999 - 2016 John Wiley & Sons, Inc.

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