171612-78-5Relevant articles and documents
Organocatalytic Multicomponent Synthesis of α/β-Dipeptide Derivatives
Martzel, Thomas,Annibaletto, Julien,Millet, Pierre,Pair, Etienne,Sanselme, Morgane,Oudeyer, Sylvain,Levacher, Vincent,Brière, Jean-Fran?ois
supporting information, p. 8541 - 8545 (2020/06/24)
A straightforward multicomponent Knoevenagel-aza-Michael-cyclocondensation reaction involving readily available hydroxamic acid-derived from naturally occurring α-amino acids allows a diversity-oriented synthesis of novel isoxazolidin-5-ones possessing an N-protected α-amino acid pendant with good to high diastereoselectivities thanks to a match effect with a chiral organocatalyst. These diversely substituted heterocycles, easily isolated as a single diastereoisomer, proved to be versatile platforms for the formation of an array of α/β-dipeptide fragments.
COMPOSITIONS HAVING ANTIMYCROBIAL ACTIVITY INCLUDING A HYDROXAMATE OR A HYDROXAMATE AND A HYDROXYLAMINE
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Page/Page column 23, (2008/06/13)
Antimycorbacterial compositions are disclosed comprising at least one hydroxamate or at least one hydroxamate and at least one hydroxylamine. The preferred ratio of hydroxamate to hydroxylamines is about 100:1 to about 1:1. A method for inhibiting mycobacterial growth is also disclosed comprising the step of administering the compositions of this invention to an animal including a human.