Hantzsch and Schiff’s reaction: synthesis, in vitro cytotoxic and antimicrobial activity of [1,3,4]oxadiazoline and [1,3]thiazole derivatives

Author:

Chidananda N.,Poojary Boja,Sumangala V.,Suchetha Kumari N.,Unnikrishnan

Publisher

Springer Science and Business Media LLC

Subject

Organic Chemistry,General Pharmacology, Toxicology and Pharmaceutics

Reference30 articles.

1. Abdel LE, Bondock S (2006) Utilization of α-halocarbonyl compounds in the synthesis of thiazole, thiadiazole and thiophene derivatives. Heteroatom Chem 17:299–305

2. Bell FW, Cantrell AS, Hogberg M, Jaskunas SR, Johansson NG, Jordon CL, Kinnick MD, Lind P, Morin JM Jr, Noreen R, Oberg B, Palkowitz JA, Parrish CA, Pranc P, Sahlberg C, Ternansky RJ, Vasileff RT, Vrang L, West SJ, Zhang H, Zhou XX (1995) Phenethylthiazolethiourea (PETT) Compounds, a New Class of HIV-1 Reverse Transcriptase Inhibitors. Synthesis and basic structure-activity relationship studies of PETT analogs. J Med Chem 38:4929–4936

3. Buckingham J, Donaghy SM (1987) Chapman dictionary of organic compounds, 5th edn. Hall Publication, London

4. CCDC (811335) contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge crystallographic data centre. www.ccdc.cam.ac.uk/data_request/cif

5. Chang HL, Cho HI, Lee K-J (2001) Synthesis of [1,3,4]oxadiazoles having phenol or thiophenol group. Bull Kor Chem Soc 22:1153–1155

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