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Synthesis and Identification of a Novel 6,5,6-Tricyclic Lactam.

✍ Scribed by Joel P. Cooper; Jeff E. Cobb; Barry G. Shearer; Douglas J. Minick; Randy D. Rutkowske


Publisher
John Wiley and Sons
Year
2003
Weight
131 KB
Volume
34
Category
Article
ISSN
0931-7597

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The stereoselective synthesis of two precursors of tricyclic Ξ²-ring-forming reaction followed by the reduction of a functionalized aromatic substituent at C-4 of the Ξ²-lactam lactam antibiotics (trinems) has been attempted by a novel approach that involves a highly stereoselective azetidinone nucleu

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