✦ LIBER ✦

s-Triazines. III. Synthesis of dihalogenoheteroaryl-s-triazines. Reaction of 2,4,6-trichloro-s-triazine with pyrrole, thiophene, and furan

✍ Scribed by Jiban K. Chakrabarti; David E. Tupper

Book ID: 112123195
Publisher: Journal of Heterocyclic Chemistry
Year: 1974
Tongue: English
Weight: 281 KB
Volume: 11
Category: Article
ISSN: 0022-152X
DOI: 10.1002/jhet.5570110329

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

s-triazines—VII : Synthesis of dihalogen

s-triazines—VII : Synthesis of dihalogeno-heteroaryl-s-triazines. Reaction of 2,4,6-trichloro-s-triazine with N-heteroaromatic rings

✍ J.K. Chakrabarti; D.E. Tupper 📂 Article 📅 1975 🏛 Elsevier Science 🌐 French ⚖ 402 KB

s-Triazines. VI. Novel reaction products

s-Triazines. VI. Novel reaction products from s-triazinylation of 2-acyl-1-methylpyrroles using 2,4,6-trichloro-s-triazine

✍ Chakrabarti, Jiban K.; Tupper, David E. 📂 Article 📅 1975 🏛 American Chemical Society 🌐 English ⚖ 268 KB

Spectrophotometric determination of glyc

Spectrophotometric determination of glycine with 2,4,6-trichloro-s-triazine

✍ Suzuki, Shuichi.; Hachimori, Yutaka.; Yaoeda, Uichi. 📂 Article 📅 1970 🏛 American Chemical Society 🌐 English ⚖ 369 KB

Sulfanilamido-s-triazines. I. Synthesis

Sulfanilamido-s-triazines. I. Synthesis of 2-Sulfanilamido-4,6-diethyl-s-triazine and Related Compounds

✍ Taft, W. E.; Krazinski, H. M.; Schaefer, F. C.; Shepherd, R. G. 📂 Article 📅 1965 🏛 American Chemical Society 🌐 English ⚖ 738 KB

Reaction of nitriles with phosgene. III.

Reaction of nitriles with phosgene. III. New synthesis of 2-chloro-4,6-diaryl-s-triazines

✍ Yanagida, Shozo; Hayama, Hiroshi; Yokoe, Masaaki; Komori, Saburo 📂 Article 📅 1969 🏛 American Chemical Society 🌐 English ⚖ 382 KB

Triazine isocyanates: Part II: Reaction

Triazine isocyanates: Part II: Reaction of 2,4-diamino-s-triazines with ethyl chlorocarbonate

✍ E. F. J. Duynstee; Th. Veerkamp 📂 Article 📅 2010 🏛 Elsevier Science 🌐 English ⚖ 504 KB

## Abstract Benzoguanamine (2,4‐diamino‐6‐phenyl‐s‐triazine) and acetoguanamine (2,4‐diamino‐6‐methyl‐s‐triazine) both react with an excess of ethyl chlorocarbonate; in this reaction two hydrogen atoms from the guanamines are replaced by two carbethoxy groups. The I.R. spectrum reveals that this do