An approach was developed for the synthesis of 5'-branched neplanocin A, as potential inhibitors against S-adenosyl-L-homocysteine hydrolase. The vinyl-stannane system of the key synthetic intermediate (14) in the present study, was prepared by radical-mediated sulfur-extrusive stannylation.
Synthesis of 5'-branched neplanocin A analogues based on radical-mediated sulfur-extrusive stannylation. Publishing Authors By Initials
Synthesis of 5'-branched neplanocin A analogues based on radical-mediated sulfur-extrusive stannylation. Journal Published:
PUBLICATION TYPE: Research Support, Non-U.S. Gov
Journal: Nucleic acids symposium series (2004)
VOLUME:
Page Numbers: 145-6
Journal Abbreviation: Nucleic Acids Symp Ser (Oxf)
ISSN: 1746-8272
DAY: 21
MONTH: 11
YEAR: 2007
Synthesis of 5'-branched neplanocin A analogues based on radical-mediated sulfur-extrusive stannylation. Information
Number of References:
LANGUAGE: eng
NlmUniqueID: 101259965
Synthesis of 5'-branched neplanocin A analogues based on radical-mediated sulfur-extrusive stannylation. Keywords Mesh Terms:
KEYWORDS:
MESH TERMS:
Chemical & Substance for Abstract: Synthesis of 5'-branched neplanocin A analogues based on radical-mediated sulfur-extrusive stannylation. Information
Substance Name:
Registry Number:
Grant and Affiliation Information for Synthesis of 5'-branched neplanocin A analogues based on radical-mediated sulfur-extrusive stannylation.
AFFILIATION: School of Pharmaceutical Sciences, Showa University, 1-5-8 Hatanodai, Shinagawa-ku, Tokyo 142-8555, Japan. kumamoto@pharm.showa-u.ac.jp
Country: England
AGENCY:
GRANT:
ACRONYM:
MEDLINETA: Nucleic Acids Symp Ser (Oxf)
REFSOURCE:
DATABASENAME:
ACCESSION NUMBER:
Number Hits: 0
Synthesis of 5'-branched neplanocin A analogues based on radical-mediated sulfur-extrusive stannylation Related Publications