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  Efficient synthesis of [2CH2]-tetrahydrodicranenone B and a 3-oxa-analogue resistant against ß-oxidation

Lauchli, R., & Boland, W. (2003). Efficient synthesis of [2CH2]-tetrahydrodicranenone B and a 3-oxa-analogue resistant against ß-oxidation. Tetrahedron, 59(2), 149-153. doi:10.1016/S0040-4020(02)01484-9.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-0012-A180-C Version Permalink: https://hdl.handle.net/21.11116/0000-0005-D938-8
Genre: Journal Article

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 Creators:
Lauchli, R.1, Author           
Boland, W.1, Author           
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1Department of Bioorganic Chemistry, MPI for Chemical Ecology, Max Planck Society, ou_24028              

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 Abstract: A short efficient synthesis of two analogues of tetrahydrodicranenone B as well as a formal synthesis of tetrahydrodicranenone B (1) itself has been devised. The approach is based on an addition/elimination sequence of in situ prepared organocuprates to

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 Dates: 2003
 Publication Status: Issued
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 Identifiers: Other: BOL367
DOI: 10.1016/S0040-4020(02)01484-9
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Title: Tetrahedron
  Other : Tetrahedron
Source Genre: Journal
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Publ. Info: Oxford : Pergamon
Pages: - Volume / Issue: 59 (2) Sequence Number: - Start / End Page: 149 - 153 Identifier: ISSN: 0040-4020
CoNE: https://pure.mpg.de/cone/journals/resource/954925448773