139397-07-2Relevant academic research and scientific papers
A practical diastereoselective synthesis of (?)-bestatin
Shang, Suisheng,Willems, Andreas V.,Chauhan, Satendra S.
, (2018/02/16)
Diastereoselective addition of nitromethane to Boc-D-Phe-H in the presence of sodium hydride in diethyl ether/hexane containing 15-crown-5 and subsequent N,O-protection with 2,2-dimethoxypropane gave trans-oxazolidine in a diastereomeric ratio of >16:1. T
Asymmetric reaction of simple nitro compounds with chiral 1,3-oxazolidin-2-ones
Kudyba, Iwona,Raczko, Jerzy,Jurczak, Janusz
, p. 1724 - 1736 (2007/10/03)
The chiral oxazolidinone 1 (=[(3aS,6R,7aR)-tetrahydro-8,8-dimethyl-2-oxo4H- 3a,6-methano-1,3-benzoxazol-3-yl](oxo)acetaldehyde) was found to react stereoselectively with simple nitro compounds in the presence of Al 2O3 or Bu4/s
Asymmetric Nitroaldol Reaction. Synthesis of Taxotere Side Chain and (-)-Bestatin Using (1R)-8-Phenylmenthyl Glyoxylate
Kudyba, Iwona,Raczko, Jerzy,Jurczak, Janusz
, p. 2844 - 2850 (2007/10/03)
The nitroaldol reaction of (1R)-8-phenylmenthyl glyoxylate (3b) with 1-nitro-1-phenylmethane (4) or with 1-nitro-2-phenylethane (13) led stereoselectively to adducts syn-2b and syn-12b, which were then transformed into the Taxotere side chain and (-)-best
Synthesis of (-)-bestatin and the Taxotere side-chain via nitroaldol reaction of (1R)-8-phenylmenthyl glyoxylate
Kudyba, Iwona,Raczko, Jerzy,Jurczak, Janusz
, p. 8685 - 8687 (2007/10/03)
The nitroaldol reaction of (1R)-8-phenylmenthyl glyoxylate 6 with 1-nitro-2-phenylethane or with phenylnitromethane led stereoselectively to adducts 4 and 12, which where then transformed into (-)-bestatin hydrochloride and the Taxotere side-chain in over
Development of selective tight-binding inhibitors of leukotriene A4 hydrolase
Yuan,Munoz,Wong,Haeggstrom,Wetterholm,Samuelsson
, p. 211 - 220 (2007/10/02)
Leukotriene A4 hydrolase is a zinc-containing enzyme which exhibits both epoxide hydrolase and aminopeptidase activities. Since the enzyme product leukotriene B4 is an inflammatory mediator, it is of interest to develop selective inh
Tuftsin derivatives
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, (2008/06/13)
Linear or cyclic tetra peptide derivatives of tuftsin which activate immunocompetent cells, i.e., macrophages and polymorphonuclear leukocyte, provide a host-mediated inhibition of the growth of tumors, provide protective effects for infectious diseases s
