✦ LIBER ✦

A novel rearrangement attending the addition of sulfenes to 1,3-bis(dimethylamino)-3-phenyl-1-propene

✍ Scribed by Leo A. Paquette; Melvin Rosen

Book ID: 104223717
Publisher: Elsevier Science
Year: 1967
Tongue: French
Weight: 258 KB
Volume: 8
Category: Article
ISSN: 0040-4039
DOI: 10.1016/s0040-4039(00)90577-x

No coin nor oath required. For personal study only.

✦ Synopsis

When a sulfene is generated in the presence of an enamine, a considerable propensity for cycloaddition to a B-aminothietsne dioxide exists (1). The most obvious feature of ' N CH312 ,I M 2, e 0 CH C6H5C"S02 8 I.

📜 SIMILAR VOLUMES

Stereochemistry of the [2+2]-cycloadditi

Stereochemistry of the [2+2]-cycloaddition of sulfene to E-1-dimethylamino-1-phenyl-1-propene. Crystal and molecular structure of E-3-dimethylamino-2-methyl-3-phenylthietane 1,1-dioxide

✍ D. S. Yufit; Yu. T. Struchkov; L. N. Koikov; P. B. Terent'ev; Yu. G. Bundel' 📂 Article 📅 1983 🏛 Springer US 🌐 English ⚖ 241 KB

ChemInform Abstract: Lewis Acid Promoted

ChemInform Abstract: Lewis Acid Promoted Addition of 1,3-Bis(silyl)propenes to Aldehydes: A Route to 1,3-Dienes.

✍ Tessie Borg; Pavel Tuzina; Peter Somfai 📂 Article 📅 2011 🏛 John Wiley and Sons ⚖ 34 KB 👁 1 views

2,3-Di(phenylsulfinyl)-1,3-butadiene via

2,3-Di(phenylsulfinyl)-1,3-butadiene via a double [2,3]-sigmatropic rearrangement of the bis-sulfenate ester of 2-butyne-1,4-diol.

✍ S. Jeganathan; William H. Okamura 📂 Article 📅 1982 🏛 Elsevier Science 🌐 French ⚖ 133 KB

Tandem carbolithiation/cyclization of 2-

Tandem carbolithiation/cyclization of 2-(3-phenyl-2-propen-1-yl) oxazolines. A novel route to cyclobutane derivatives

✍ Ralph P. Robinson; Brian J. Cronin; Brian P. Jones 📂 Article 📅 1997 🏛 Elsevier Science 🌐 French ⚖ 192 KB

ChemInform Abstract: Tandem Carbolithiat

ChemInform Abstract: Tandem Carbolithiation/Cyclization of 2-(3-Phenyl-2-propen-1-yl)oxazolines. A Novel Route to Cyclobutane Derivatives.

✍ R. P. ROBINSON; B. J. CRONIN; B. P. JONES 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 35 KB 👁 2 views

Diastereoselective formation of 2,3,4,5-

Diastereoselective formation of 2,3,4,5-tetrasubstituted tetrahydrofurans by a Lewis acid promoted addition of C3-substituted 1,3-bis(silyl)propenes to aldehydes

✍ Borg, Tessie; Timmer, Brian; Somfai, Peter 📂 Article 📅 2013 🏛 Elsevier Science 🌐 French ⚖ 416 KB