| Literature DB >> 10814147 |
.
Abstract
On the basis of a pyrrolidine tweezer 1, a library of peptidosulfonamide tweezers (15a-e, 16a-e) was synthesized on the solid phase. This library was screened in a simultaneous substrate screening procedure for the ability to enantioselectively catalyze the Ti(O-i-Pr)(4)-mediated addition of diethylzinc to aldehydes. One of the best solid-phase tweezer catalyst (i.e., 16d, giving an ee of 32% in solid-phase catalysis) was resynthesized in solution (compounds 20 and 21). The now homogeneous solution-phase catalysis showed even better enantioselectivity (i.e., up to 66%).Entities:
Year: 2000 PMID: 10814147 DOI: 10.1021/jo991628z
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354