1 H and  13 C NMR study of 5‐substituted‐4‐ (arylidene)amino‐2,4‐dihydro‐3 H ‐1,2,4‐triazole‐3‐thiones and 6‐aryl‐3‐( D ‐gluco‐ pentitol‐1‐yl)‐7 H ‐1,2,4‐triazolo[3,4‐b] [1,3,4]thiadiazines | Zendy

Zhang Anjiang | Zendy; Zhang Lixue | Zendy; Lei Xinxiang | Zendy

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1 H and 13 C NMR study of 5‐substituted‐4‐ (arylidene)amino‐2,4‐dihydro‐3 H ‐1,2,4‐triazole‐3‐thiones and 6‐aryl‐3‐( D ‐gluco‐ pentitol‐1‐yl)‐7 H ‐1,2,4‐triazolo[3,4‐b] [1,3,4]thiadiazines

Author(s) -

Zhang Anjiang,

Zhang Lixue,

Lei Xinxiang

Publication year - 2006

Publication title -

magnetic resonance in chemistry

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.483

H-Index - 72

eISSN - 1097-458X

pISSN - 0749-1581

DOI - 10.1002/mrc.1829

Subject(s) - chemistry , aryl , proton nmr , triazole , stereochemistry , medicinal chemistry , combinatorial chemistry , organic chemistry , alkyl

Five 5‐substituted‐4‐(arylidene)amino‐2,4‐dihydro‐3 H ‐1, 2,4‐triazole‐3‐thiones (2a–2e) and seven 6‐aryl‐3‐( D ‐gluco‐pentitol‐1‐yl)‐7 H ‐1,2,4‐triazolo[3,4‐b][1,3,4]thiadiazines (3a–3g) were synthesized. The complete 1 H and 13 C NMR chemical shift assignments were analyzed on one‐ and two‐dimensional NMR techniques, including DEPT, NOE‐DIF, COSY, gHMBC, and gHSQC. Copyright © 2006 John Wiley & Sons, Ltd.

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