88816-46-0Relevant academic research and scientific papers
Stereoselective Synthesis of a (5R,6S)-6--2-thioxopenam Ester through a Hydroxy Group Directed Chlorinolysis
Daniels, Nick,Johnson, Graham,Ross, Barry C.
, p. 1006 - 1007 (1983)
Hydroxy group directed chlorinolysis of (3S,4R)-3--4-ethylthioazetidin-2-one (4) gives predominantly the corresponding (4S)-4-chloroazetidinone (5) which is cyclised to the (5R,6S)-6--2-thioxopenam (1).
7-Oxo-4-thia-1-azabicyclo(3,2,0)heptane derivatives
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, (2008/06/13)
Compounds of the formula Ia and their tautomers Ib STR1 in which formulae R represents a carboxyl esterifying group are described, as well as processes for their manufacture. Ia and Ib are valuable starting materials for the preparation of various derivatives substituted at position 3 that possess antibacterial properties.
