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Studies Toward Communesin F: A Diels-Alder Approach.

Danielsson, Jakob LU and Somfai, Peter LU (2014) In Organic Letters 16(3). p.784-787
Abstract
A Diels-Alder reaction is used as a key step in a synthetic study toward communesin F, in order to simultaneously introduce both of the all-carbon quaternary stereocenters with complete control of relative stereochemistry. Further manipulations of the cycloadduct, toward the hexacyclic core-structure of communesin F, are also disclosed.
Please use this url to cite or link to this publication:
author
and
organization
publishing date
type
Contribution to journal
publication status
published
subject
in
Organic Letters
volume
16
issue
3
pages
784 - 787
publisher
The American Chemical Society (ACS)
external identifiers
  • pmid:24446678
  • wos:000331163900037
  • scopus:84893842050
  • pmid:24446678
ISSN
1523-7052
DOI
10.1021/ol403516s
language
English
LU publication?
yes
id
c2207252-1aca-422e-b076-8f90531f018f (old id 4290992)
date added to LUP
2016-04-01 09:53:20
date last changed
2025-10-14 11:43:56
@article{c2207252-1aca-422e-b076-8f90531f018f,
  abstract     = {{A Diels-Alder reaction is used as a key step in a synthetic study toward communesin F, in order to simultaneously introduce both of the all-carbon quaternary stereocenters with complete control of relative stereochemistry. Further manipulations of the cycloadduct, toward the hexacyclic core-structure of communesin F, are also disclosed.}},
  author       = {{Danielsson, Jakob and Somfai, Peter}},
  issn         = {{1523-7052}},
  language     = {{eng}},
  number       = {{3}},
  pages        = {{784--787}},
  publisher    = {{The American Chemical Society (ACS)}},
  series       = {{Organic Letters}},
  title        = {{Studies Toward Communesin F: A Diels-Alder Approach.}},
  url          = {{http://dx.doi.org/10.1021/ol403516s}},
  doi          = {{10.1021/ol403516s}},
  volume       = {{16}},
  year         = {{2014}},
}