134038-71-4Relevant academic research and scientific papers
Total synthesis of the biphenomycins; II. Synthesis of protected (2S,4R)-4-hydroxyornithines
Schmidt,Meyer,Leitenberger,Stabler,Lieberknecht
, p. 409 - 413 (1991)
Improved synthetic methods for the preparation of three differently protected (2S,4R)-4-hydroxyornithine (10, 16, 24) have been developed which obviously can be used for the construction of the other stereoisomers. Formation of the corresponding α,β-dideh
Process for preparing chiral (s)-2,3-disubstituted-1-propylamine derivatives
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, (2008/06/13)
A process for the preparation of chiral (S)-2,3-disubstituted-1-propylamine derivatives, in which a carbonyl group of (S) 3,4-disubstituted-1-butanecarbonyl derivatives is converted to an amine group, and the conversion reaction is performed through Curti
The Synthesis of Biphenomycin B
Schmidt, Ulrich,Meyer, Regina,Leitenberger, Volker,Lieberknecht, Albrecht,Griesser, Helmut
, p. 275 - 277 (2007/10/02)
Biphenomycin B, a highly potent antibiotic against Gram-negative, β-lactam-resistant bacteria, which was previously isolated from culture filtrates of Streptomyces griseorubiginosus No. 43708, has now been synthesized.
