Synthesis and biological evaluation of (acyl)hydrazones and thiosemicarbazones obtained via in situ condensation of iminium salts with nitrogen-containing nucleophiles-Reference-Cited by-同舟云学术

Synthesis and biological evaluation of (acyl)hydrazones and thiosemicarbazones obtained via in situ condensation of iminium salts with nitrogen-containing nucleophiles

Published:2015-06-16 Issue:4 Volume:19 Page:669-684
ISSN:1381-1991
Container-title:Molecular Diversity
language:en
Short-container-title:Mol Divers

Author:

Caneva Chiara,Alfei Silvana,De Maria Monica,Ibba Cristina,Delogu Ilenia,Spallarossa Andrea,Loddo Roberta

Publisher

Springer Science and Business Media LLC

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Drug Discovery,Molecular Biology,General Medicine,Information Systems,Catalysis

Link

http://link.springer.com/content/pdf/10.1007/s11030-015-9597-z.pdf

Reference48 articles.

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2. Meth-Cohn O, Tarnowski B (1982) Cyclizations under Vilsmeier conditions. Adv Heterocycl Chem 31:207–236. doi: 10.1016/S0065-2725(08)60399-2

3. Selvi S, Perumal PT (1999) Synthetic utility of Vilsmeier Reaction: more vinamidinium salts. Synth Commun 29:73–77. doi: 10.1080/00397919908085737

4. Thompson BB (1968) The Mannich Reaction. Mechanistic and technological considerations. J Pharm Sci 57:715–733. doi: 10.1002/jps.2600570501

5. Prout FS, Beaucaire VD, Dyrkacz GR, Koppes WM, Kuznicki RE, Marlewski TA, Pienkowski JJ, Puda JM (1973) Knoevenagel Reaction. Kinetic study of the reaction of (+)-3-methyl-cyclohexanone with malononitrile. J Org Chem 38:1512–1517. doi: 10.1021/jo00948a015

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