A simple preparation of N, N-dimethyl-N′-alkyl (aryl) sulfonylformamidines
…, A Covarrubias-Zuniga, LA Maldonado
Index: Silva, A. L.; Covarrubias-Zuniga, A.; Maldonado, L. A. Organic Preparations and Procedures International, 2002 , vol. 34, # 5 p. 545 - 549
Full Text: HTML
Citation Number: 7
Abstract
Melting points are uncorrected. IR spectra (KBr or film) were carried out on a FT-Nicolet SX apparatus.'H NMR (300 MHz) and 13C NMR (75 MHz) spectra were recorded on a Varian VXR 300 spectrometer with TMS as internal standard. CDC1, was used as solvent for la, lb, and lc and CDC1,-DMSO-d6 for Id.
Related Articles:
[Fukuda, Tsutomu; Iwao, Masatomo Heterocycles, 2012 , vol. 86, # 2 p. 1261 - 1273]
THE ACTION OF ACID CHLORIDES UPON TRIMETHYLAMINE1
[Jones; Whalen Journal of the American Chemical Society, 1925 , vol. 47, p. 1347]
[Malik, Sarika; Nadir, Upender K.; Pandey, Pramod S. Synthetic Communications, 2008 , vol. 38, # 18 p. 3074 - 3081]
Multinuclear NMR study of variously substituted sulphonamides and sulphinamides
[Ruosteuso, P.; Haekkinen, A.-M.; Mattila, T. Magnetic Resonance in Chemistry, 1987 , vol. 25, p. 189 - 193]
[Fukuda, Tsutomu; Iwao, Masatomo Heterocycles, 2012 , vol. 86, # 2 p. 1261 - 1273]