Chiral synthesis of 5-hydroxy-(L)-pipeco
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Patrick D Bailey; Justin S Bryans
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Article
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1988
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Elsevier Science
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French
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A stereo-and enantio-specific synthesis of the natural1 occurring cis-%hydroxy-(L)-pipecolic acid (3) is described, starting from Z-(L -glutamic the key step involves c chsation of a Y, to trans-%hydroxy-(L -pipecolic acl 3 3 rotected chlorohydrin, and also gives access acid, .