Hydroxycyclopentanone derivatives from D-Mannose via ring closing metathesis: An improved synthesis of a key intermediate of Tricyclo-DNA
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BORIS DOI
Publisher DOI
Description
A large scale, 10 step synthesis of cyclopentanone 1 , starting from the chiral pool compound D-mannose, is described. The synthesis proceeds via a ring closing metathesis reaction as the key step in an overall yield of 23%. Cyclopentanone 1 is a central intermediate for the synthesis of tricyclo-DNA
Date of Publication
2003
Publication Type
article
Subject(s)
500 - Science::570 - Life sciences; biology
500 - Science::540 - Chemistry
Keyword(s)
large-scale
synthesis
tricyclo-DNA
synthesis
tricyclo-DNA
Language(s)
en
Additional Credits
Departement für Chemie und Biochemie (DCB)
Series
Synthesis - journal of synthetic organic chemistry
Publisher
Thieme
ISSN
0039-7881
Access(Rights)
restricted