English
 
Help Privacy Policy Disclaimer
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT

Released

Journal Article

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

MPS-Authors
/persons/resource/persons4008

Lauchli,  R.
Department of Bioorganic Chemistry, MPI for Chemical Ecology, Max Planck Society;

/persons/resource/persons3812

Boland,  W.
Department of Bioorganic Chemistry, MPI for Chemical Ecology, Max Planck Society;

External Resource
No external resources are shared
Fulltext (public)
There are no public fulltexts stored in PuRe
Supplementary Material (public)
There is no public supplementary material available
Citation

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.


Cite as: http://hdl.handle.net/11858/00-001M-0000-0012-A180-C
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