Tetrahedron letters

Preparation of 1-alkynyl 2-(trimethylsilyl) ethyl sulfides as thiolate anion precursors for self-assembled monolayers

…, S Shimada, S Ohnishi, F Nakanishi, H Matsuda

Index: Takeda, Hiroyuki; Shimada, Satoru; Ohnishi, Satomi; Nakanishi, Fusae; Matsuda, Hiro Tetrahedron Letters, 1998 , vol. 39, # 22 p. 3701 - 3704

Full Text: HTML

Citation Number: 32

Abstract

Syntheses of 1-alkynyl 2-(trimethylsilyl) ethyl sulfides are reported. Deprotection of 2- (trimethylsilyl) ethyl groups using fluoride ions permits the formation of thiolate anions which are trapped by in situ alkylation with methyl iodide and can be used to produce self- assembled monolayers on gold.

Related Articles:

Reaction of 1??alkynyl thiocyanates with nucleophilic reagents. Synthesis of 2, 4??disubstituted 1, 3??thiazoles

[Jong, R.L.P. de; Meijer, J.; Sukhai, R.S.; Bradsma, L. Recueil: Journal of the Royal Netherlands Chemical Society, 1982 , vol. 101, # 9 p. 310 - 313]

Reaction of 1??alkynyl thiocyanates with nucleophilic reagents. Synthesis of 2, 4??disubstituted 1, 3??thiazoles

[Jong, R.L.P. de; Meijer, J.; Sukhai, R.S.; Bradsma, L. Recueil: Journal of the Royal Netherlands Chemical Society, 1982 , vol. 101, # 9 p. 310 - 313]

More Articles...