๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Ketonization of 2-hydroxy-2,4-pentadienoate by 4-oxalocrotonate tautomerase: implications for the stereochemical course and the mechanism

โœ Scribed by Lian, Huiling; Whitman, Christian P.


Book ID
126922797
Publisher
American Chemical Society
Year
1993
Tongue
English
Weight
822 KB
Volume
115
Category
Article
ISSN
0002-7863

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


Enzymatic kinetic resolution of (ยฑ)-4-ac
โœ Antonio Cipiciani; Francesco Fringuelli; Vittorio Mancini; Oriana Piermatti; Ann ๐Ÿ“‚ Article ๐Ÿ“… 1997 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 305 KB

The enzymatic kinetic resolution of (-+)-4-acetoxy122]paracyclophane by Candida cylindracea lipase was investigated in water and in a two-phase aqueous organic system. The (+)-(R)-4-hydroxy-and (+)-(S)-4-acetoxyl2,2l-paracyclophanes were isolated in excellent yields and high enantiomeric excesses. T

Mechanisms of toxicity of 2- and 5-hydro
โœ Mary D'Arcy Doherty; Adrian Rodgers; Gerald M. Cohen ๐Ÿ“‚ Article ๐Ÿ“… 1987 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 569 KB

The mechanisms of toxicity to isolated rat hepatocytes of two structurally related naphthoquinones have been studied. Both 5-OH-1,4-naphthoquinone (5-OH-1,4-NQ; juglone) and 2-OH-1,4-naphthoquinone (2-OH-1,4-NQ; lawsone) caused a concentration-dependent cytotoxicity to hepatocytes which was preceded