View : 13 Download: 0

Stereoselective synthesis of 3-hydroxymethyl-D-cyclopentenone, the versatile intermediate for the synthesis of carbocyclic nucleosides

Title
Stereoselective synthesis of 3-hydroxymethyl-D-cyclopentenone, the versatile intermediate for the synthesis of carbocyclic nucleosides
Authors
Choi W.J.Moon H.R.Kim H.O.Ko Y.M.Kim H.J.Lee J.A.Lee K.M.Yun M.K.Shin D.H.Chun M.W.Sheen Y.Y.Kim K.Jeong L.S.
Ewha Authors
이강만신윤용정낙신
SCOPUS Author ID
이강만scopus; 신윤용scopus
Issue Date
2005
Journal Title
Nucleosides, Nucleotides and Nucleic Acids
ISSN
1525-7770JCR Link
Citation
vol. 24, no. 41401, pp. 611 - 613
Indexed
SCIE; SCOPUS WOS scopus
Abstract
The preparative and stereoselective synthesis (45-50% overall yields, >50 g scale) of the key carbasugars 7a-d was achieved from D-ribose via stereoselective Grignard reaction and oxidative rearrangement as key reactions. Copyright © Taylor & Francis, Inc.
DOI
10.1081/NCN-200061832
Appears in Collections:
약학대학 > 약학과 > Journal papers
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