| Literature DB >> 21894881 |
Andrew G Schafer1, Joshua M Wieting, Anita E Mattson.
Abstract
Silanediols are introduced as a new class of hydrogen bond donor catalysts for the activation of nitroalkenes toward nucleophilic attack. Excellent yields of product are obtained for the conjugate addition of indole to β-nitrostyrene catalyzed with a stable, storable dinaphthyl-derived silanediol. The preparation and structural characterization of a C(2)-symmetric chiral silanediol is also reported along with its ability to catalyze the conjugate addition reaction.Entities:
Year: 2011 PMID: 21894881 DOI: 10.1021/ol2021115
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005