✦ LIBER ✦

Studies with Polyfunctionality Substituted Heterocycles: Novel Syntheses of Thienopyrimido-1,2,4-triazoles

✍ Scribed by El-Gazzar, A. B. A.; Hegab, M. I.; Swelam, S. A.; Aly, A. S.

Book ID: 120396714
Publisher: Taylor and Francis Group
Year: 2002
Tongue: English
Weight: 153 KB
Volume: 177
Category: Article
ISSN: 1042-6507
DOI: 10.1080/10426500210219

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Studies with Polyfunctionally Substitute

Studies with Polyfunctionally Substituted Heterocycles: Syntheses of Polyfunctionally Substituted Isoquinolines

✍ Y. M. Elkholy 📂 Article 📅 2002 🏛 Springer US 🌐 English ⚖ 130 KB

Studies with Polyfunctionally Substitute

Studies with Polyfunctionally Substituted Heterocycles: Syntheses of Polyfunctionally Substituted Isoquinolines.

✍ Yehya M. Elkholy 📂 Article 📅 2003 🏛 John Wiley and Sons ⚖ 121 KB

## Abstract For Abstract see ChemInform Abstract in Full Text.

Syntheses of substituted-1,2,4-triazoles

✍ A. Shafiee; F. Naghashian; N. Reghabi 📂 Article 📅 1992 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 181 KB

991. Triazoles. Part VII. Syntheses of s

991. Triazoles. Part VII. Syntheses of substituted 1,2,4-triazoles

✍ Browne, E. J. ;Polya, J. B. 📂 Article 📅 1962 🏛 The Royal Society of Chemistry ⚖ 425 KB

Syntheses of 1-substituted 1,2,4-triazol

Syntheses of 1-substituted 1,2,4-triazoles, imidazoles and benzimidazoles

✍ Abdollah Sharifian; Kaykavoos Parang; Hassan Zorrieh-Amirian; Mehrdad Nazarinia; 📂 Article 📅 1994 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 186 KB

Concise and regiospecific syntheses of t

Concise and regiospecific syntheses of tri-substituted 1,2,4-triazoles

✍ Andrew R Dunstan; Hans-Peter Weber; Grety Rihs; Hans Widmer; Edward K Dziadulewi 📂 Article 📅 1998 🏛 Elsevier Science 🌐 French ⚖ 180 KB

Novel tri-substituted 1,2,4-triazoles are synthesized via complementary, regiospecific routes as part of a lead finding exercise. A key feature of one of the syntheses is recognition of an intrinsic regioselectivity toward deprotonation in the 1-phenylguanazole substrate.