Photodimerization of N-benzyl-1,4-dihydronicotinamide
โ Scribed by Giorgio Adembri; Alfredo Camparini; Donato Donati; Stefania Fusi; Fabio Ponticelli; Mirella Scotton
- Publisher
- Elsevier Science
- Year
- 1983
- Tongue
- French
- Weight
- 201 KB
- Volume
- 24
- 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
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
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