๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Flavin catalyzed reduction of diaryl disulfide with 1-benzyl-1,4-dihydronicotinamide

โœ Scribed by Ken Fujimori; Toshiyuki Nagata; Shigeru Oae


Publisher
Elsevier Science
Year
1983
Tongue
French
Weight
120 KB
Volume
24
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

โœฆ Synopsis


din&&den were hound Xo be teduced bmootkey to Xhc c~~netkio.R~ by BNAff a ca&Cy.tic amount 06 3-mtihy&?umi#auin undeh mad conditions. The redox reaction between thiol and disulfide is very important in living bodies. 2)(eq.l) This reaction is promoted by emzymes, such as lipoamide dehydrogenase, glutathione reductase, thioredoxin reductase, which possess commonly FAD and cystine residue at their active sites. 3) CONH2 Flavin


๐Ÿ“œ SIMILAR VOLUMES


Reduction of diaryl disulfides with 1-be
โœ Shigeru Oae; Toshiyuki Nagata; Toshiaki Yoshimura; Ken Fujimori ๐Ÿ“‚ Article ๐Ÿ“… 1982 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 229 KB

sumtnmy : Redution 06 dicvry1 dAuR,jideA with I-benzyt-l,4-dihydtronicofivmmide (ENAH] ptoceeded &tough a had-&at chain heation, wkiee di.a.tkyL dhu&du wem dound to be inat to BNAH. Thiols, such as glutathione, and redox enzymes whose active site possesses two cysteine residues in proximity, reduce

Reduction of hexachloroacetone by 1-benz
โœ Donald C. Dittmer; Louis J. Steffa; John R. Potoski; Roger A. Fouty ๐Ÿ“‚ Article ๐Ÿ“… 1961 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 138 KB

HEXACHLOROACETONE is very readily reduced to hexachloroisopropanol by I-benzyl-l,f+-dihydronicotinamide. The reduction goes violently at room and is accompanied went vigorously. temperature in the absence of solvent, is exothermic, by formation of a black tar. Even at 0' the reaction cc13cocc13 + HC

Reactions of dihydronicotinamides II. Th
โœ James J. Steffens; John P. Cross; David M. Chipman ๐Ÿ“‚ Article ๐Ÿ“… 1972 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 219 KB

02139 (R8ceived in IJR 12 Cctober 1972; acoepted for publication 26 Octobar 1972) le would like to report the dimerization of I-benzyl-1,4-dihydronicotinamide in acidic aqueous suspension to form the polycyclic cage molecule 1 in high yield. Although