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Iridium/NMDPP Catalyzed Asymmetric Ring‐Opening Reaction of Oxabenzonorbornadienes with Phenolic or Naphtholic Nucleophiles

Iridium/NMDPP Catalyzed Asymmetric Ring‐Opening Reaction of Oxabenzonorbornadienes with Phenolic... Open up: An (Ir(COD)Cl)2/ (S)‐NMDPP (COD=1,5‐cyclooctadiene; NMDPP=neomenthyldiphenylphosphine) complex catalyzes asymmetric ring‐opening reactions of oxabenzonorbornadienes with phenolic or naphtholic nucleophiles efficiently. Up to 96 % yield and 88 % ee was achieved. DMF=N,N‐dimethylformamide. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Asian Journal of Organic Chemistry Wiley

Iridium/NMDPP Catalyzed Asymmetric Ring‐Opening Reaction of Oxabenzonorbornadienes with Phenolic or Naphtholic Nucleophiles

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References (51)

Publisher
Wiley
Copyright
Copyright © 2013 Wiley Subscription Services, Inc., A Wiley Company
ISSN
2193-5807
eISSN
2193-5815
DOI
10.1002/ajoc.201300077
Publisher site
See Article on Publisher Site

Abstract

Open up: An (Ir(COD)Cl)2/ (S)‐NMDPP (COD=1,5‐cyclooctadiene; NMDPP=neomenthyldiphenylphosphine) complex catalyzes asymmetric ring‐opening reactions of oxabenzonorbornadienes with phenolic or naphtholic nucleophiles efficiently. Up to 96 % yield and 88 % ee was achieved. DMF=N,N‐dimethylformamide.

Journal

Asian Journal of Organic ChemistryWiley

Published: Jun 1, 2013

Keywords: ; ; ; ;

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