✦ LIBER ✦

ChemInform Abstract: Utilization of Wieland Furoxan Synthesis for Preparation of 4-Aryl-1,2, 5-oxadiazole-3-yl Carbamate Derivatives Having Potent Anti-HIV Activity.

✍ Scribed by H. TAKAYAMA; S. SHIRAKAWA; M. KITAJIMA; N. AIMI; K. YAMAGUCHI; Y. HANASAKI; T. IDE; K. KATSUURA; M. FUJIWARA; K. IJICHI; K. KONNO; S. SIGETA; T. YOKOTA; M. BABA

Book ID: 112042050
Publisher: John Wiley and Sons
Year: 2010
Weight: 32 KB
Volume: 27
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.199652154

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Utilization of wieland furoxan synthesis

Utilization of wieland furoxan synthesis for preparation of 4-aryl-1,2,5-oxadiazole-3-yl carbamate derivatives having potent anti-HIV activity

✍ Hiromitsu Takayama; Seiichiro Shirakawa; Mariko Kitajima; Norio Aimi; Kentaro Ya 📂 Article 📅 1996 🏛 Elsevier Science 🌐 English ⚖ 218 KB

ChemInform Abstract: A One-Pot Efficient

ChemInform Abstract: A One-Pot Efficient Four-Component Reaction for the Synthesis of 2-(Arylamino)-2-(5-aryl-1,3,4-oxadiazol-2-yl)propyl Benzoate (or Acetate) Derivatives.

✍ Ali Ramazani; Yavar Ahmadi; Asemeh Mashhadi Malekzadeh; Aram Rezaei 📂 Article 📅 2012 🏛 John Wiley and Sons ⚖ 15 KB 👁 2 views

## Abstract The multicomponent reaction between oxopropylbenzoate(acetate) (I), (VI), primary amines (II), (N‐isocyanimino)triphenylphosphorane (III), and aromatic carboxylic acids (IV) proceeds smoothly at room temperature under neutral conditions to afford the sterically congested oxadiazole deri

ChemInform Abstract: The Reaction of (N-

ChemInform Abstract: The Reaction of (N-Isocyanimino)triphenylphosphorane with Biacetyl in the Presence of Aromatic Carboxylic Acids: Efficient One-Pot Three-Component Reaction for the Synthesis of 3-(5-Aryl-1,3,4-oxadiazol-2-yl)-3-hydroxybutan-2-one Derivatives (IV).

✍ Ali Ramazani; Morteza Rouhani; Aram Rezaei; Nahid Shajari; Ali Souldozi 📂 Article 📅 2011 🏛 John Wiley and Sons ⚖ 23 KB 👁 3 views

ChemInform Abstract: Highly Potent and O

ChemInform Abstract: Highly Potent and Orally Active Non-peptide Arginine Vasopressin Antagonists for Both V1A and V2 Receptors: Synthesis and Pharmacological Properties of 4′-[(4,4-Difluoro-5-methylidene-2,3,4,5-tetrahydro-1H-1-benzoazepin-1-yl )carbonyl]-2-phenylbenzanilide Derivatives.

✍ Yoshiaki Shimada; Nobuaki Taniguchi; Akira Matsuhisa; Kenichiro Sakamoto; Takeyu 📂 Article 📅 2001 🏛 John Wiley and Sons ⚖ 44 KB 👁 2 views