✦ LIBER ✦

New Compounds. Possible Anthelmintic Thiazol-5-ylbenzimidazoles. III

✍ Scribed by Singh, J

Book ID: 118048053
Publisher: American Chemical Society
Year: 1969
Tongue: English
Weight: 149 KB
Volume: 12
Category: Article
ISSN: 0022-2623
DOI: 10.1021/jm00303a631

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

New Compound. 2,5-Disubstituted Oxazoles

New Compound. 2,5-Disubstituted Oxazoles and Thiazoles

✍ Hayes, F. N.; King, L. C.; Peterson, D. E. 📂 Article 📅 1952 🏛 American Chemical Society 🌐 English ⚖ 260 KB

A new route to 6-phenyl-2,3,5,6-tetrahyd

A new route to 6-phenyl-2,3,5,6-tetrahydroimidazo[2,1-b]thiazole, a broad spectrum anthelmintic

✍ T. Bailey; T. P. Seden; R. W. Turner 📂 Article 📅 1969 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 226 KB

Possible heavy-fermion behaviour of new

Possible heavy-fermion behaviour of new U(Cu, Al)5 compounds

✍ H. Nakotte; K.H.J. Buschow; J.C.P. Klaasse; K. Prokeš; F.R. de Boer; A.V. Andree 📂 Article 📅 1995 🏛 Elsevier Science 🌐 English ⚖ 180 KB

ChemInform Abstract: trans-Myristic Acid

ChemInform Abstract: trans-Myristic Acid 3-tert-Butoxycarbonylamino-2-oxopiperidin-5-yl Ester, a New Anthelmintic Compound.

✍ L. SUESCUN P.; R. A. MARIEZCURRENA; A. W. MOMBRU; O. A. GONZALEZ; E. MANTA; S. G 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 28 KB

Synthesis of Some New 5-(2-Substituted-1

Synthesis of Some New 5-(2-Substituted-1,3-thiazol-5-yl)-2-hydroxy Benzamides and Their 2-Alkoxy Derivatives as Possible Antifungal Agents.

✍ B. Narayana; K. K. Vijaya Raj; B. V. Ashalatha; N. Suchetha Kumari; B. K. Saroji 📂 Article 📅 2005 🏛 John Wiley and Sons ⚖ 17 KB 👁 1 views

New Addition Reactions of Organometal Co

New Addition Reactions of Organometal Compounds with 4,4-Dimethyl-1,3-thiazole-5(4H)-thiones

✍ Junxing Shi; Heinz Heimgartner 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 German ⚖ 963 KB

## Abstract Addition reactions of organometallic reagents with 4,4‐disubstituted 1,3‐thiazole‐5(4__H__)‐thiones were studied. Whereas the reactions with alkyllithium and alkyl __Grignard__ reagents occurred in the thiophilic manner, the carbophilic addition was observed with allyllithium and allyl