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Journal article

Total asymmetric synthesis of sperabillins B and D.

Abstract:
A concise route to the core fragment of sperabillins B and D, methyl (3R,5R,6R)-3,6-diamino-5-hydroxyheptanoate, has been developed with a subsequent novel protection strategy allowing the total asymmetric synthesis of sperabillins B and D.
Publication status:
Published

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Publisher copy:
10.1039/b305740b

Authors


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Institution:
University of Oxford
Department:
Oxford, MPLS, Chemistry, Organic Chemistry
Mortimer, AJ More by this author
Journal:
Chemical communications (Cambridge, England)
Volume:
9
Issue:
17
Pages:
2132-2133
Publication date:
2003-09-05
DOI:
EISSN:
1364-548X
ISSN:
1359-7345
URN:
uuid:581b4fed-1757-4944-9fc2-888357bc405e
Source identifiers:
110537
Local pid:
pubs:110537
Language:
English

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