General Synthesis Route to Benanomicin??Pradimicin Antibiotics

M Tamiya, K Ohmori, M Kitamura, H Kato…

Index: Kato; Ohmori; Suzuki Synlett, 2001 , # SPEC. ISS p. 1003 - 1005

Full Text: HTML

Citation Number: 24

Abstract

Abstract A general approach to the regio-and stereoselective total synthesis of the benanomicin-pradimicin antibiotics (BpAs) is described. Construction of the aglycon has been achieved by 1) the diastereoselective ring-opening of a biaryl lactone by using (R)-

Related Articles:

1, 3, 5-Trialkyl-hexahydro-1, 3, 5-triazines–N-methylenealkylamines equilibria. 1 H NMR studies in solutions

[Adamczyk-Wozniak, Agnieszka; Bujnowski, Krzysztof; Sporzynski, Andrzej Journal of Molecular Structure, 2008 , vol. 892, # 1-3 p. 177 - 181]

1, 3, 5-Trialkyl-hexahydro-1, 3, 5-triazines–N-methylenealkylamines equilibria. 1 H NMR studies in solutions

[Adamczyk-Wozniak, Agnieszka; Bujnowski, Krzysztof; Sporzynski, Andrzej Journal of Molecular Structure, 2008 , vol. 892, # 1-3 p. 177 - 181]

More Articles...