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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
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
external identifiers
  • pmid:24446678
  • wos:000331163900037
  • scopus:84893842050
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
2014-02-27 12:48:03
date last changed
2017-08-06 03:01:55
@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},
  series       = {Organic Letters},
  title        = {Studies Toward Communesin F: A Diels-Alder Approach.},
  url          = {http://dx.doi.org/10.1021/ol403516s},
  volume       = {16},
  year         = {2014},
}