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 with N-benzyl-1,4 dihydronicotinamide. A reinvestigation.
โ Scribed by P. Tintillier; G. Dupas; J. Bourguignon; G. Queguiner
- Publisher
- Elsevier Science
- Year
- 1986
- Tongue
- French
- Weight
- 179 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0040-4039
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๐ SIMILAR VOLUMES
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
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, glu