vic-Iodothiocyanates and iodoisothiocyanates. Part 8. Addition of iodine–thiocyanogen to alkenes under ionic and radical conditions

…, PS Rutledge, GA Strange, PD Woodgate

Index: Cambie, Richard C.; Rutledge, Peter S.; Strange, Gary A.; Woodgate, Paul D. Heterocycles, 1982 , vol. 19, # 8 p. 1501 - 1510

Full Text: HTML

Citation Number: 9

Abstract

Addition of iodine–thiocyanogen to alkenes in the dark proceeds by a regioselective ionic reaction to give mainly-iodoisothiocyanates, and under irradiation with uv light by a radical reaction to give mainly-iodothiocyanates. However, in the case of 1-methylene-4-t-

Related Articles:

Rapid and efficient ring opening of epoxides catalyzed by a new electron deficient tin (IV) porphyrin

[Moghadam, Majid; Tangestaninejad, Shahram; Mirkhani, Valiollah; Shaibani, Reza Tetrahedron, 2004 , vol. 60, # 29 p. 6105 - 6111]

Catalytic Enantioselective Conversion of Epoxides to Thiiranes

[Malaschichin, Sergej; Fu, Changchun; Linden, Anthony; Heimgartner, Heinz Helvetica Chimica Acta, 2005 , vol. 88, # 12 p. 3253 - 3262]

Laser induced synthesis: selective formation of cyclohexene episulphide from molecular sulphur s 8

[Bertaina, C.; Fellous, R.; Lemaire, F.; Stringat, R. Tetrahedron Letters, 1985 , vol. 26, # 45 p. 5521 - 5522]

Dioxyphosphoranes, an Emerging Class of Versatile Reagents for Organic Synthesis

[Kelly, Jeffery W.; Robinson, Philip L.; Evans, Slayton A. Phosphorus and Sulfur and the Related Elements, 1987 , vol. 30, p. 147 - 150]

Isolation of the key intermediates in the catalyst-free conversion of oxiranes to thiiranes in water at ambient temperature

[Kleiner, Christian M.; Horst, Luise; Wuertele, Christian; Wende, Raffael; Schreiner, Peter R. Organic and Biomolecular Chemistry, 2009 , vol. 7, # 7 p. 1397 - 1403]

More Articles...