✦ LIBER ✦

1,2,3-Dithiazoles and new routes to 3,1-benzoxazin-4-ones, 3,1-benzothiazin-4-ones and N-arylcyanothioformamides

✍ Scribed by Besson, Thierry; Emayan, Kumaraswamy; Rees, Charles W.

Book ID: 120024154
Publisher: Royal Society of Chemistry
Year: 1995
Weight: 806 KB
Volume: 17
Category: Article
ISSN: 1472-7781
DOI: 10.1039/P19950002097

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: 1,2,3-Dithiazoles a

ChemInform Abstract: 1,2,3-Dithiazoles and New Routes to 3,1-Benzoxazin-4-ones, 3,1- Benzothiazin-4-ones and N-Arylcyanothioformamides.

✍ T. BESSON; K. EMAYAN; C. W. REES 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 28 KB

3,1-Benzoxazin-4-ones, 3,1-benzothiazin-

3,1-Benzoxazin-4-ones, 3,1-benzothiazin-4-ones and N-arylcyanothioformamides

✍ Besson, Thierry; Emayan, Kumaraswamy; Rees, Charles W. 📂 Article 📅 1995 🏛 The Royal Society of Chemistry 🌐 English ⚖ 204 KB

Antimicrobial evaluation of 3,1-benzoxaz

Antimicrobial evaluation of 3,1-benzoxazin-4-ones, 3,1-benzothiazin-4-ones, 4-alkoxyquinazolin-2-carbonitriles and N-arylimino-1,2,3-dithiazoles

✍ Thierry Besson; Charles W. Rees; Gilles Cottenceau; Anne-Marie Pons 📂 Article 📅 1996 🏛 Elsevier Science 🌐 English ⚖ 275 KB

ChemInform Abstract: Antimicrobial Evalu

ChemInform Abstract: Antimicrobial Evaluation of 3,1-Benzoxazin-4-ones, 3,1-Benzothiazin-4- ones, 4-Alkoxyquinazolin-2-carbonitriles and N-Arylimino-1,2,3- dithiazoles.

✍ T. BESSON; C. W. REES; G. COTTENCEAU; A.-M. PONS 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 29 KB 👁 1 views

3,1-Benzothiazin-4-ones and 3,1-Benzoxaz

3,1-Benzothiazin-4-ones and 3,1-Benzoxazin-4-ones: Highly Different Activities in Chymotrypsin Inactivation

✍ U. Neumann; M. Gutschow 📂 Article 📅 1995 🏛 Elsevier Science 🌐 English ⚖ 822 KB

3.1-Benzothiazin-4-ones are sulfur analogs of the potent serine protease inactivators of the 3,1-benzoxazin-4-one type. which acylate the serine residue within the active site of the enzymes. A series of 2-amino-3,1-benzothiazinones was synthesized, but these compounds showed only very little inhibi

4H-3,1-Benzoxazin-4-ones methoxy-substit

4H-3,1-Benzoxazin-4-ones methoxy-substituted 2-(2-arenesulfonylaminophenyl)-4H-3,1-benzoxazin-4-ones

✍ M. V. Loseva; B. M. Bolotin; B. M. Krasovitskii 📂 Article 📅 1971 🏛 Springer US 🌐 English ⚖ 273 KB