Highly enantioselective intramolecular copper catalyzed C-H insertion reactions of alpha-diazosulfones.

Typeset version

 

TY  - JOUR
  - Flynn, CJ; Elcoate, CJ; Lawrence, SE; Maguire, AR
  - 2010
  - February
  - Journal of the American Chemical Society
  - Highly enantioselective intramolecular copper catalyzed C-H insertion reactions of alpha-diazosulfones.
  - Validated
  - ()
  - 132
  - 4
  - 1184
  - 1185
  - Excellent enantiocontrol (up to 98% ee) is achieved in copper catalyzed C-H insertions of alpha-diazosulfones to form thiopyrans, with up to 60% ee in C-H insertions leading to sulfolanes.
  - 10.1021/ja909713a
DA  - 2010/02
ER  - 
@article{V5956739,
   = {Flynn, CJ and  Elcoate, CJ and  Lawrence, SE and  Maguire, AR},
   = {2010},
   = {February},
   = {Journal of the American Chemical Society},
   = {Highly enantioselective intramolecular copper catalyzed C-H insertion reactions of alpha-diazosulfones.},
   = {Validated},
   = {()},
   = {132},
   = {4},
  pages = {1184--1185},
   = {{Excellent enantiocontrol (up to 98% ee) is achieved in copper catalyzed C-H insertions of alpha-diazosulfones to form thiopyrans, with up to 60% ee in C-H insertions leading to sulfolanes.}},
   = {10.1021/ja909713a},
  source = {IRIS}
}
AUTHORSFlynn, CJ; Elcoate, CJ; Lawrence, SE; Maguire, AR
YEAR2010
MONTHFebruary
JOURNAL_CODEJournal of the American Chemical Society
TITLEHighly enantioselective intramolecular copper catalyzed C-H insertion reactions of alpha-diazosulfones.
STATUSValidated
TIMES_CITED()
SEARCH_KEYWORD
VOLUME132
ISSUE4
START_PAGE1184
END_PAGE1185
ABSTRACTExcellent enantiocontrol (up to 98% ee) is achieved in copper catalyzed C-H insertions of alpha-diazosulfones to form thiopyrans, with up to 60% ee in C-H insertions leading to sulfolanes.
PUBLISHER_LOCATION
ISBN_ISSN
EDITION
URL
DOI_LINK10.1021/ja909713a
FUNDING_BODY
GRANT_DETAILS