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Cited by 477

The DOI matches its Crossref record; 8 of the 8 references it cites were found in a registry or an index.

Enantioselective Heck Arylations of Acyclic Alkenyl Alcohols Using a Redox-Relay Strategy

Open access
Werner, Erik W., Mei, Tian-Sheng, Burckle, Alexander J., Sigman, Matthew S.·2012·Science

Abstract

From C=C to C=O: The palladium-catalyzed Heck reaction is widely used to form carbon-carbon bonds between aryl rings and olefins, after which elimination of a hydrogen atom restores the olefin's double bond. Werner et al. (p. 1455 ; see the Perspective by Gilbertson ) present a variant of this reaction in which a hydrogen atom is instead lost from an alcohol center elsewhere in the molecule, yielding a ketone and a chiral center where the arene is bound. The process is highly enantioselective and also versatile: The alcohol can be sited one, two, or even three carbons away from the olefin.

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Metadata

Authors
Werner, E. W., Mei, T.-S., Burckle, A. J., & Sigman, M. S.
Venue
Science
Published
2012-12-14
Volume
338
Issue
6113
Pages
1455-1458
ISSN
  • 0036-8075 (ISSN-L)
  • 1095-9203
OpenAlex
W1992002089
Cited by
477
References
8
FWCI
11.96
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Enantioselective Heck Arylations of Acyclic Alkenyl Alcohols Using a Redox-Relay Strategy. https://app.cochat.ai/papers/10.1126/science.1229208
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Werner, E. W., Mei, T.-S., Burckle, A. J., & Sigman, M. S. (2012). Enantioselective Heck Arylations of Acyclic Alkenyl Alcohols Using a Redox-Relay Strategy. Science. https://doi.org/10.1126/science.1229208

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