Stereocontrolled synthesis of anticancer β-lactams via the Staudinger reaction

2005 ◽  
Vol 13 (11) ◽  
pp. 3611-3622 ◽  
Author(s):  
Bimal K. Banik ◽  
Indrani Banik ◽  
Frederick F. Becker
ChemInform ◽  
2010 ◽  
Vol 33 (19) ◽  
pp. no-no
Author(s):  
Seema Kanwar ◽  
Aarti Saluja ◽  
J. P. S. Khurana ◽  
S. D. Sharma

1985 ◽  
Vol 50 (14) ◽  
pp. 2416-2423 ◽  
Author(s):  
Joseph P. Michael ◽  
Pauline C. Ting ◽  
Paul A. Bartlett

ACS Omega ◽  
2021 ◽  
Author(s):  
Kazuki Sato ◽  
Tomoya Hagio ◽  
Michi Sano ◽  
Kazumasa Muramoto ◽  
Aya Yaoita ◽  
...  

ChemInform ◽  
2010 ◽  
Vol 31 (5) ◽  
pp. no-no
Author(s):  
Alessandra Maria Nocioni ◽  
Carmela Papa ◽  
Claudia Tomasini

Molecules ◽  
2019 ◽  
Vol 24 (11) ◽  
pp. 2177
Author(s):  
Antonia Di Mola ◽  
Consiglia Tedesco ◽  
Antonio Massa

Herein we describe a very useful application of the readily available trifunctional aromatic ketone methyl-2-(2-bromoacetyl)benzoate in reactions with primary amines. An unexpected in situ air oxidation that follows a cascade process allowed the access to a series of isoquinoline-1,3,4(2H)-triones, a class of heterocyclic compounds of great interest containing an oxygen-rich heterocyclic scaffold. A modification of the original protocol, utilizing a Staudinger reaction in the presence of trimethylphosphine, was necessary for the synthesis of Caspase inhibitor trione with free NH group.


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