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Studies towards the synthesis of lindenene: Unexpected stereochemical outcome of an intramolecular cyclopropanation reaction and synthesis of (+/-)-epi-Lindenene and (+/-)-iso-Lindenene

Abstract:
Investigation towards the synthesis of the furanosesquiterpene Lindenene using an intramolecular cyclopropanation reaction gave unexpected ring-junction isomerisation products. These products were elaborated to (±)-epi- lindenene and (±)-iso-lindenene. © Georg Thieme Verlag Stuttgart.
Publication status:
Published

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Publisher copy:
10.1055/s-2007-991069

Authors


More by this author
Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Sub department:
Organic Chemistry
Role:
Author


Journal:
SYNLETT More from this journal
Volume:
2007
Issue:
17
Pages:
2679-2682
Publication date:
2007-10-16
DOI:
EISSN:
1437-2096
ISSN:
0936-5214


Language:
English
Keywords:
Pubs id:
pubs:40587
UUID:
uuid:19385613-2ece-47e5-8b3b-4a4aed5507b6
Local pid:
pubs:40587
Source identifiers:
40587
Deposit date:
2013-11-16

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