Synthesis of enantiopure isoprene epoxides from (S)-lactic acid via 'dispoke'intermediates
…, C Bleasdale, BT Golding, WP Watson
Index: Zhang, Daping; Bleasdale, Christine; Golding, Bernard T.; Watson, William P. Chemical Communications, 2000 , # 13 p. 1141 - 1142
Full Text: HTML
Citation Number: 9
Abstract
The mechanistic toxicology of isoprene is a subject of considerable current importance. 1 In this context, samples of single enantiomers of isoprene epoxides are required for the preparation of reference standards of DNA adducts. We describe efficient syntheses of enantiomerically pure (S)-2-ethenyl-2-methyloxirane 1 and (2R,2′S)-2-methylbioxirane 2, using as starting material the 'dispoke protected lactate' 3 derived from (S)-lactic acid. 2 An eight-step synthesis of ...
Related Articles:
[Barner; Hubscher Helvetica Chimica Acta, 1983 , vol. 66, # 3 p. 880 - 890]