## Abstract magnified image A series of novel 6‐aryl‐3‐(1,2,3,4‐tetrahydroxybutanol‐1‐yl)‐7__H__‐1,2,4‐triazolo[3,4‐__b__][1,3,4]thiadiazines were easily synthesized in high yields by means of the reactions of 4‐amino‐5‐(1,2,3,4‐tetrahydroxybutyl)‐2,4‐dihydro‐3__H__‐1,2,4‐triazole‐3‐thione (**1**)
Selective activation of apoptosis by a novel set of 4-aryl-3-(3-aryl-1-oxo-2-propenyl)-2(1H)-quinolinones through a Myc-dependent pathway
✍ Scribed by Gisela Claassen; Elena Brin; Candace Crogan-Grundy; Mei Ting Vaillancourt; Han Zhong Zhang; Sui Xiong Cai; John Drewe; Ben Tseng; Shailaja Kasibhatla
- Book ID
- 116334999
- Publisher
- Elsevier Science
- Year
- 2009
- Tongue
- English
- Weight
- 616 KB
- Volume
- 274
- Category
- Article
- ISSN
- 0304-3835
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## Abstract The N‐substituted 1‐benzimidazolyl‐succinimides **6a**–**v** (Scheme 1, Table 1 and 2) have been prepared by the reaction of benzimidazole and its derivatives with maleimides. Reduction of the N‐cyclohexyl and N‐cyclo‐octyl substituted 1‐benzimidazolyl‐succinimides **6i**–**k** with lit