Synthesis of optically active ene carbamates from chromium carbene complexes: use in palladium(II)-assisted synthesis of relays to (+)-thienamycin

1990 ◽  
Vol 112 (17) ◽  
pp. 6255-6263 ◽  
Author(s):  
John Montgomery ◽  
Gary M. Wieber ◽  
Louis S. Hegedus
1990 ◽  
Vol 112 (3) ◽  
pp. 1109-1117 ◽  
Author(s):  
Louis S. Hegedus ◽  
Rene Imwinkelried ◽  
Marie Alarid-Sargent ◽  
Dalimil Dvorak ◽  
Yoshitaka Satoh

The photochemical reaction of chromium carbene complexes with imines has been developed into an efficient process for the synthesis of β-lactams. A new route to aminocarbene complexes, involving the reaction of Na 2 Cr(CO) 5 with amides and trimethylsilyl chloride has been developed. By using this procedure, chiral, optically active aminocarbene complexes have been prepared, and their photochemical reactions with imines developed. Chiral, optically active β-lactams have been prepared with more than 90% diastereoselectivity by this procedure. Chiral, optically active aminocarbene complexes containing pendent alcohol groups have also been prepared. Photolysis of these produces aminolactones, which can be cleaved to natural and unnatural α-amino acids.


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