scholarly journals Synthetic Studies of Carbapenem and Penem Antibiotics. VI. Stereoselective Reduction of Enamino Ketone and Lactonization of the Reduction Product for the Synthesis of 1.BETA.-Methylcarbapenem.

1994 ◽  
Vol 42 (12) ◽  
pp. 2467-2471 ◽  
Author(s):  
Haruki MATSUMURA ◽  
Yoshihito NOZAKI ◽  
Makoto SUNAGAWA
Keyword(s):  
Reduction Product ◽  
Enamino Ketone ◽  
Stereoselective Reduction ◽  
Synthetic Studies

ChemInform Abstract: Synthetic Studies of Carbapenem and Penem Antibiotics. Part 4. Stereoselective Reduction of 3-Acetyl-2-azetidinone with Aminoalkoxyborane.

ChemInform ◽  
2010 ◽  
Vol 24 (40) ◽  
pp. no-no
Author(s):  
M. SUNAGAWA ◽  
T. YANO ◽  
S. TAKATA ◽  
T. INOUE ◽  
A. SASAKI ◽  
...  
Keyword(s):  
Stereoselective Reduction ◽  
Synthetic Studies

scholarly journals Synthetic Studies of Carbapenem and Penem Antibiotics. IV. Stereoselective Reduction of 3-Acetyl-2-azetidinone with Aminoalkoxyborane.

1992 ◽  
Vol 40 (11) ◽  
pp. 3076-3078 ◽  
Author(s):  
Makoto SUNAGAWA ◽  
Tsuneo YANO ◽  
Shinji TAKATA ◽  
Takaaki INOUE ◽  
Akira SASAKI ◽  
...  
Keyword(s):  
Stereoselective Reduction ◽  
Synthetic Studies

Synthetic studies toward inducamide C

2021 ◽  
Author(s):  
Ardalan A. Nabi ◽  
Lydia M. Scott ◽  
Daniel P. Furkert ◽  
Jonathan Sperry
Keyword(s):  
Natural Product ◽  
Structural Revision ◽  
Synthetic Studies

The rare benzoxazepine ring in the alkaloid inducamide C is unstable and prone to rearrangement, indicating that structural revision of the natural product may be necessary.

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