NEWER ROUTE FOR THE SYNTHESIS OF β-PHENYLTHIO, β-PHENYLSULFINYL AND β-PHENYLSULFONYL NITROETHYLENES

V Ramamoorthy, S Sivasubramanian…

Index: Ramamoorthy; Sivasubramanian; Muthusubramanian Organic Preparations and Procedures International, 1997 , vol. 29, # 2 p. 207 - 210

Full Text: HTML

Citation Number: 3

Abstract

Olefins substituted with either nitro or sulfur functions have been shown to behave as excellent dienophiles in Diels-Alder reactions and as acceptors in Michael addition reactions.'Thus olefins substituted with both nitro and sulfur functions at each end of the double bond might be very useful synthons in organic synthesis. They should be reactive as Michael acceptors and/or dienophilesZa and the nitro and sulfur functions can be ...

Related Articles:

Borax-catalyzed thiolysis of 1, 2-epoxides in aqueous medium

[Gao, Peng; Xu, Peng-Fei; Zhai, Hongbin Tetrahedron Letters, 2008 , vol. 49, # 46 p. 6536 - 6538]

Cobalt mediated regioselective ring opening of oxiranes with benzenethiol: A mechanistic study

[Iqbal, Javed; Pandey, Anu; Shukla, Alka; Srivastava, Rajiv Ranjan; Tripathi, Sanjay Tetrahedron, 1990 , vol. 46, # 18 p. 6423 - 6432]

AUSTRALIAN JOURNAL OF

[Bandgar, Babasaheb P.; Joshi, Neeta S.; Kamble, Vinod T.; Sawant, Sanjay S. Australian Journal of Chemistry, 2008 , vol. 61, # 3 p. 231 - 234]

New Synthetic Route for the Preparation of 4-Phenylthio-4-butanolide Derivatives by the Use of the Pummerer Rearrangement

[Watanabe, Mikio; Nakamori, Seijin; Hasegawa, Hatsue; Shirai, Kozo; Kumamoto, Takanobu Bulletin of the Chemical Society of Japan, 1981 , vol. 54, # 3 p. 817 - 821]

Highly regioselective and stereospecific functionalization of 1, 2-propanediol with trimethyl (X) silanes employing the 1, 3, 2. lambda. 5-dioxaphospholane …

[Mathieu-Pelta, Isabel; Evans, Slayton A. Journal of Organic Chemistry, 1992 , vol. 57, # 12 p. 3409 - 3413]

More Articles...