Studies Toward Communesin F: A Diels-Alder Approach.
(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:
https://lup.lub.lu.se/record/4290992
- author
- Danielsson, Jakob LU and Somfai, Peter LU
- organization
- publishing date
- 2014
- 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
- 2022-04-27 08:29:54
@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}}, }