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ID 70009
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Author
Hanaya, Tadashi Department of Chemistry, Faculty of Science, Okayama University Kaken ID publons researchmap
Schürrle, Karsten Department of Chemistry, Faculty of Science, Okayama University
Yamamoto, Hiroshi Department of Chemistry, Faculty of Science, Okayama University
Abstract
Treatment of 1,4-di-O-mesyl-2,3-di-O-methyl-L-threitol (8b) with phenylphosphine in the presence of sodium hydride in DMSO, followed by the action of hydrogen peroxide, afforded 3,4-dimethoxy-1-phenylphospholane 1- oxide (7), while the same treatment of 1,5-di-O-mesyl-2,3,4-tri-O-methyl-meso- xylitol (11b) provided 2,3,4-trimethoxy-1-phenylphosphorinane 1-oxide (14).
Published Date
2006
Publication Title
HETEROCYCLES
Volume
volume69
Issue
issue1
Publisher
The Japan Institute of Heterocyclic Chemistry
Start Page
283
End Page
294
ISSN
0385-5414
NCID
AA00663739
Content Type
Journal Article
language
English
OAI-PMH Set
岡山大学
Copyright Holders
© The Japan Institute of Heterocyclic Chemistry
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publisher
DOI
Web of Science KeyUT
Related Url
isVersionOf https://doi.org/10.3987/com-06-s(o)28
License
https://creativecommons.org/licenses/by-nc-nd/4.0/