Skip to content
RDL
Network
Ekosistem
Uygulama değiştir
EN
Hakkımızda
SSS
Giriş yap
Başla
Enantioselective Synthesis of γ‐Hydroxyenones by Chiral Base‐Catalyzed Kornblum DeLaMare Rearrangement. — Steven T. Staben (2007) | RDL Network
Back
Cite
Save
Save for later
Share
Home
Publications
Enantioselective Synthesis of γ‐Hydroxyenones by Chiral Base‐Catalyzed Kornblum DeLaMare Rearrangement.
Shared by
Dean Toste
University of California, Berkeley
Enantioselective Synthesis of γ‐Hydroxyenones by Chiral Base‐Catalyzed Kornblum DeLaMare Rearrangement.
Article
2007
en
Authors
SS
Steven T. Staben
XL
Xin Linghu
Dean Toste
University of California, Berkeley
Abstract
1 min read
Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
Discussion
(0)
Sign in
to like and join the discussion.
No comments yet. Be the first to comment.
Related publications
Article
2006
Stereoselective Synthesis of Vinylsilanes by a Gold(I)‐Catalyzed Acetylenic Sila‐Cope Rearrangement.
Yoshikazu Horino
,
Michael R. Luzung
,
Dean Toste
Article
2007
Rearrangement of Alkynyl Sulfoxides Catalyzed by Gold(I) Complexes.
Nathan D. Shapiro
,
Dean Toste
Article
2007
Rearrangement of Alkynyl Sulfoxides Catalyzed by Gold(I) Complexes.
Nathan D. Shapiro
,
Dean Toste
Article
2006
Enantioselective Synthesis of Cyclic Ethers Through a Vanadium‐Catalyzed Resolution/Oxidative Cyclization.
Aurélien Blanc
,
Dean Toste
Article
2007
Regioselective and Enantioselective Iridium‐Catalyzed Allylation of Enamines.
Daniel J. Weix
,
John F Hartwig
Discussion(0)
No comments yet. Be the first to comment.