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Enantioselective Synthesis of Benzyl (1 S ,2 R ,4 R )-4-( tert -Butoxycarbonylamino)-2-(hydroxymethyl)cyclohexylcarbamate Using an Iodolactamization As the Key Step

✍ Scribed by Campbell, Carlton L.; Hassler, Carla; Ko, Soo S.; Voss, Matthew E.; Guaciaro, Michael A.; Carter, Percy H.; Cherney, Robert J.


Book ID
126994624
Publisher
American Chemical Society
Year
2009
Tongue
English
Weight
758 KB
Volume
74
Category
Article
ISSN
0022-3263

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## An efficient stereoselective synthesis of Z-(2S)-and Z-(2R)-2-tert-butoxycarbonylamino -6-hydroxyhex-4-enoic acid, key intermediates in the synthesis of (2S,4S,5R)-(-)-and (2R,4R,5S)-(+)-bulgecinine