Document Detail


Enantioselective Conjugate Addition of Alkenylboronic Acids to Indole-Appended Enones.
MedLine Citation:
PMID:  21846131     Owner:  NLM     Status:  Publisher    
Abstract/OtherAbstract:
An enantioselective addition of alkenylboronic acids and alkynylboronic esters to unprotected indole-appended enones is reported. This transformation proceeds with high enantioselectivity and high product yields via the use of catalytic amounts of 3,3'-bis(pentafluorophenyl)-BINOL and Mg(Ot-Bu)(2). A range of α-branched indole derivatives are available from the transformation.
Authors:
Brian J Lundy; Santa Jansone-Popova; Jeremy A May
Publication Detail:
Type:  JOURNAL ARTICLE     Date:  2011-8-16
Journal Detail:
Title:  Organic letters     Volume:  -     ISSN:  1523-7052     ISO Abbreviation:  -     Publication Date:  2011 Aug 
Date Detail:
Created Date:  2011-8-17     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  100890393     Medline TA:  Org Lett     Country:  -    
Other Details:
Languages:  ENG     Pagination:  -     Citation Subset:  -    
Affiliation:
Department of Chemistry, University of Houston , Houston, Texas 77204-5003, United States.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Organic Triplet Excited States of Gold(I) Complexes with Oligo(o- or m-phenyleneethynylene) Ligands:...
Next Document:  Lysozyme adsorption on polyethylene surfaces: why are long simulations needed?