Selective Protonation at a C−F Bond in the Presence of an Iridium−Methyl Bond Gives Diastereoselective Carbon−Fluorine Bond Activation and Carbon−Carbon Bond Formation. A New Path to Carbon Stereocenters Bearing Fluorine Atoms-Reference-Cited by-同舟云学术

Selective Protonation at a C−F Bond in the Presence of an Iridium−Methyl Bond Gives Diastereoselective Carbon−Fluorine Bond Activation and Carbon−Carbon Bond Formation. A New Path to Carbon Stereocenters Bearing Fluorine Atoms

Published:2002-10-11 Issue:23 Volume:21 Page:4902-4904
ISSN:0276-7333
Container-title:Organometallics
language:en
Short-container-title:Organometallics

Author:

Hughes Russell P.¹,Zhang Donghui¹,Zakharov Lev N.¹,Rheingold Arnold L.¹

Affiliation:

1. Departments of Chemistry, 6128 Burke Laboratory, Dartmouth College, Hanover, New Hampshire 03755, and University of Delaware, Newark, Delaware 19716

Publisher

American Chemical Society (ACS)

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/om020718i

Reference34 articles.

1. Synthetic Applications of Electrophilic Fluorodesilylation

2. Electrophilic Fluorination Mediated by Cinchona Alkaloids: Highly Enantioselective Synthesis of α-Fluoro-α-phenylglycine Derivatives

3. The Mechanism of Catalytic Enantioselective Fluorination: Computational and Experimental Studies

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