Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/45411
Title: Stereoselective epoxidation of aziridin-2-acrylaldehydes and azirinols synthesized from epoxyaldehydes catalyzed by NHC catalyst
Authors: Jin, Zhunian
Keywords: Aziridine-epoxyaldehydes;Stereoselective epoxidation;Azirinols;Ring opening reaction;NHC catalyst
Issue Date: Nov-2018
Publisher: NISCAIR-CSIR, India
Abstract: Chiral aziridine-epoxyaldehydes (d.r. up to 99:1) have been obtained from stereoselective epoxidation of aziridin-2-acrylaldehyde in the presence of proline-derivatived catalyst. The desired aziridine-epoxyaldehydes can give valuable azirinols via ring opening reaction catalyzed by NHC catalyst. These azirinol derivatives are good candidates for the synthesis of more functionalized structures.
Page(s): 1409-1415
URI: http://nopr.niscair.res.in/handle/123456789/45411
ISSN: 0975-0983(Online); 0376-4699(Print)
Appears in Collections:IJC-B Vol.57B(11) [November 2018]

Files in This Item:
File Description SizeFormat 
IJCB 57B(11) 1409-1415.pdf322.14 kBAdobe PDFView/Open


Items in NOPR are protected by copyright, with all rights reserved, unless otherwise indicated.