4.8 Article

Nickel-Catalyzed Enantioselective C-C Bond Formation through C-sp2-O Cleavage in Aryl Esters

Journal

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
Volume 54, Issue 13, Pages 4075-4078

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201412051

Keywords

aryl esters; C-O cleavage; C-O electrophiles; nickel catalysis

Funding

  1. ICIQ foundation
  2. European Research Council [ERC-277883]
  3. MINECO [CTQ2012-34054]
  4. MINECO (Severo Ochoa Excellence Accreditation) [SEV-2013-0319]
  5. CELLEX Foundation through the CELLEX-ICIQ high-throughput experimentation platform
  6. European Union [FP7-PEOPLE-2012-IEF-328381]
  7. Rackham Graduate School
  8. ICREA Funding Source: Custom

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We report the first enantioselective C-C bond formation through C-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.

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