| Literature DB >> 28868655 |
Christian Simon Gloor1, Fabrice Dénès2, Philippe Renaud1.
Abstract
An efficient and simple radical chain reaction to convert terminal alkynes into arenesulfonylmethylcyclopentanes is described. The reaction involves a radical addition-translocation-cyclization process and necessitates solely the use of readily available arenesulfonyl chlorides in tetrahydrofuran. Interestingly, this radical-mediated C-H activation process took place with a high level of retention of configuration when an enantiomerically pure starting material was used.Entities:
Keywords: cyclization; hydrosulfonylation; radicals; sulfonyl chlorides; tetrahydofuran
Year: 2017 PMID: 28868655 DOI: 10.1002/anie.201707791
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336