Synthesis of 2-substituted 3,4-dihydroquinazoline derivatives via regioselective addition of a carbon nucleophile to a carbodiimide

Authors
Lee, BHLee, JYChung, BYLee, YS
Issue Date
2004-01-01
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Citation
HETEROCYCLES, v.63, no.1, pp.95 - +
Abstract
Synthesis of 2-alkyl or phenyl-substituted 3,4-dihydroquinazoline derivatives (6) is described via regioselective carbon nucleophilic addition (RMgBr and RM) to a carbodiimide (4) followed by intramolecular conjugate addition.
Keywords
CONJUGATED HETEROCUMULENES; STRATEGY; FACILE; CONJUGATED HETEROCUMULENES; STRATEGY; FACILE; 3,4-dihydroquinazoline; carbon nucleophile; Grignard reagent; carbodiimide; regioselectivity
ISSN
0385-5414
URI
https://pubs.kist.re.kr/handle/201004/137945
Appears in Collections:
KIST Article > 2004
Files in This Item:
There are no files associated with this item.
Export
RIS (EndNote)
XLS (Excel)
XML

qrcode

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

BROWSE