STEREOSELECTIVE MICHAEL ADDITIONS OF NITROMETHANE YIELDING 3R(1S N-SUBSTITUTED AMINOETHYL)PYRROLIDINES

Authors
PLUMMER JS EMERY LA STIER MA SUTO MJ
Citation
Js. Plummer et al., STEREOSELECTIVE MICHAEL ADDITIONS OF NITROMETHANE YIELDING 3R(1S N-SUBSTITUTED AMINOETHYL)PYRROLIDINES, Tetrahedron letters, 34(47), 1993, pp. 7529-7532
Citations number
8
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron letters → ACNP
ISSN journal
00404039
Volume
34
Issue
47
Year of publication
1993
Pages
7529 - 7532
Database
ISI
SICI code
0040-4039(1993)34:47<7529:SMAONY>2.0.ZU;2-A
Abstract
The 1,4-addition of nitromethane to vinylogous esters of N-protected a mino acids proceeded with good to excellent yields and with good diast ereoselectivity.