Action of (2-benzothiazolyl) methyllithium with organic polar functions

@inproceedings{Costa1991ActionO,
  title={Action of (2-benzothiazolyl) methyllithium with organic polar functions},
  author={Maria Virg{\'i}nia Costa and Alain Brembilla and Denis Roizard and Pierre Lochon},
  year={1991}
}
  • Maria Virgínia Costa, Alain Brembilla, +1 author Pierre Lochon
  • Published 1991
  • Chemistry
  • (2-Benzothiazolyl)methyllithium reacts quickly at low temperature (-78 o ) with a variety of organic electrophiles like aldehydes, ketones, carboxylic esters, nitriles and acyl chlorides. Such reactions lead to an easy introduction of alcohol, keto-enol or amine-enamine functional groups in extracyclic position with a stereoselective preference. These polyfunctional compounds whose synthesis is difficult by other pathways, are interesting, in particular, because of their ability to form… CONTINUE READING

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