✦ LIBER ✦

1,2,4-Thiadiazole-3,5-dicarbonitrile by Reaction of Cyanogen with Sulfur

✍ Scribed by Prof. Dr. Herbert W. Roesky; Klaus Keller; Dr. Jan. W. Bats

Publisher: John Wiley and Sons
Year: 1983
Tongue: English
Weight: 117 KB
Volume: 22
Category: Article
ISSN: 0044-8249
DOI: 10.1002/anie.198308811

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

1,2,4-Thiadiazol-3,5-dicarbonitril durch

1,2,4-Thiadiazol-3,5-dicarbonitril durch Reaktion von Dicyan mit Schwefel

✍ Prof. Dr. Herbert W. Roesky; Klaus Keller; Dr. Jan W. Bats 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 130 KB 👁 1 views

1,2,4-Thiadiazol-3,5-dicarbonitril durch

1,2,4-Thiadiazol-3,5-dicarbonitril durch Reaktion von Dicvan mit Schwefel

✍ Herbert W. Roesky; Klaus Keller; Jan W. Bats 📂 Article 📅 1983 🏛 John Wiley and Sons 🌐 English ⚖ 165 KB

Reaktionen von 1,2,4-Thiadiazol-3,5-dica

Reaktionen von 1,2,4-Thiadiazol-3,5-dicarbonitril und Röntgenstrukturanalyse von 3-Cyan-1,2,4-thiadiazol-5-carboximidsäure-methylester

✍ Roesky, Herbert W. ;Hofmann, Hartmut ;Keller, Klaus ;Pinkert, Waltraud ;Jones, P 📂 Article 📅 1984 🏛 Wiley (John Wiley & Sons) 🌐 English ⚖ 257 KB

Eingegangen am 6. Oktober 1983 Aus 1,2,4-Thiadiazol-3,5-dicarbonitril(1) werden die Imidsaureester 2.4, die Thioamide 3.6 und das Dicarboxarnid 5 erhalten. Dabei wird die unterschiedliche Reaktivitat der beiden Nitrilgruppen von 1 gegenuber nucleophilen Reagenzien ausgenutzt. Zuerst erfolgt der Angr

Synthesis of 2-amino-5-(1-methyl-5-nitro

Synthesis of 2-amino-5-(1-methyl-5-nitro-[4-3H]-2-imidazolyl)-1,3,4-thiadiazole

✍ G. Chauviere; B. Rousseau; F. Pillon; J. Perie 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 French ⚖ 237 KB 👁 1 views

Reactions with hydrazonoyl halides XXVII

Reactions with hydrazonoyl halides XXVIII*: Synthesis of some 2-thiazolylimino-2,3-dihydro-1,3,4-thiadiazoles

✍ Abdou O. Abdelhamid; Nadia A. Abdel-Riheem; Nabil M. Hassan 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 163 KB 👁 1 views

## Hydrazonoyl halides have been caused to react with each of methyl 5-ethoxycarbonyl-4-methylthiazole-2-aminothiocarbamate, benzyl 5-ethoxycarbonyl-4-methylthiazole-2-aminothiocarbamate, and 5-ethoxycarbonyl-4-methylthiazol-2-ylphenylthiourea in the presence of triethylamine to give 2-imino-(5-eth

Synthesis of 3-Phenyl-, 3,4-Diphenyl-, a

Synthesis of 3-Phenyl-, 3,4-Diphenyl-, and 3-(β-Naphthyl)-1,2,5-thiadiazole

✍ Dr. V. Bertini; Prof. Dr. P. Pino 📂 Article 📅 1965 🏛 John Wiley and Sons 🌐 English ⚖ 117 KB 👁 1 views

Acyl chlorides are split into acyl and chlorine radicals by light of wavelength 254 my. Since the dissociation energy of the chlorine-hydrogen bond is considerably larger than that of the acyl-hydrogen bond, substitution of the substrate by acyl radicals is observed on irradiation of acid chlorides.