Use of 2, 3-bis (phenylsulfonyl)-1-propene as a multicoupling reagent

A Padwa, DN Kline, SS Murphree…

Index: Padwa, Albert; Kline, Donald N.; Murphree, S. Shaun; Yeske, Philip E. Journal of Organic Chemistry, 1992 , vol. 57, # 1 p. 298 - 306

Full Text: HTML

Citation Number: 24

Abstract

Once a monoadduct is formed, a new reactive site is present in the product. The introduction of an aminecontaining pendant functionality would provide an avenue for further chemical manipulation. One attractive subsequent reaction appeared to be the use of a suitable halide precursor for a radical ring closure. Cyclization reactions involving free-radical chain processes are rapidly gaining ground in the repertoire of synthetic In the construction of ...

Related Articles:

Catalyst-free alkylation of sulfinic acids with sulfonamides via sp3 C− N Bond cleavage at room temperature

[Liu, Cong-Rong; Li, Man-Bo; Cheng, Dao-Juan; Yang, Cui-Feng; Tian, Shi-Kai Organic Letters, 2009 , vol. 11, # 12 p. 2543 - 2545]

Iron-catalyzed cross-coupling of unactivated secondary alkyl thio ethers and sulfones with aryl Grignard reagents

[Denmark, Scott E.; Cresswell, Alexander J. Journal of Organic Chemistry, 2013 , vol. 78, # 24 p. 12593 - 12628]

Catalytic Enantioselective Oxidation of Bulky Alkyl Aryl Thioethers with H2O2 over Titanium–Salan Catalysts

[Bryliakov, Konstantin P.; Talsi, Evgenii P. European Journal of Organic Chemistry, 2011 , # 24 p. 4693 - 4698]

A novel method for the synthesis of aryl sulfones

[Steensma, Ruo W.; Galabi, Sharen; Tagat, Jayaram R.; McCombie, Stuart W. Tetrahedron Letters, 2001 , vol. 42, # 12 p. 2281 - 2283]

Mechanistic organic chemistry in a microreactor. Zeolite-controlled photooxidations of organic sulfides

[Lamothe; Anderson; Fuchs Synthetic Communications, 1991 , vol. 21, # 15-16 p. 1675 - 1693]

More Articles...