2-Naphthalenesulfonyl as a tosyl substitute for protection of amino functions. Cyclic voltammetry studies on model sulfonamides and their preparative cleavage by …
…, HLS Maia, LS Monteiro, U Ragnarsson
Index: Maia, Hernani L. S.; Monteiro, Luis S.; Degerbeck, Fredrik; Grehn, Leif; Ragnarsson, Ulf Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), 1993 , # 3 p. 495 - 500
Full Text: HTML
Citation Number: 35
Abstract
With the aim to develop a practically useful, reductively more labile alternative to tosyl for protection of amino functions, initially a number of N-arenesulfonyl-protected heterocycles (pyrroles, imidazoles, indole, and carbazole) have been prepared and studied by cyclic voltammetry (CV). The recorded activation potentials vary from-1.32 to-1.99 V (vs SCE). In N- sulfonylazolides such as tosylindole the cathodic potentials are shifted by over 0.5 V ...
Related Articles:
[Ohta, Akihiro; Inagawa, Yukiko; Mitsugi, Chie Journal of Heterocyclic Chemistry, 1985 , vol. 22, p. 1643 - 1646]
[Ohta, Akihiro; Inagawa, Yukiko; Mitsugi, Chie Journal of Heterocyclic Chemistry, 1985 , vol. 22, p. 1643 - 1646]
Synthetic and structural studies on 1, 2, 4-dithiazolidine-3, 5-dione derivatives
[Wood, Mark E.; Cane-Honeysett, Daniel J.; Dowle, Michael D.; Coles, Simon J.; Hursthouse, Michael B. Organic and Biomolecular Chemistry, 2003 , vol. 1, # 17 p. 3015 - 3023]
Synthetic and structural studies on 1, 2, 4-dithiazolidine-3, 5-dione derivatives
[Wood, Mark E.; Cane-Honeysett, Daniel J.; Dowle, Michael D.; Coles, Simon J.; Hursthouse, Michael B. Organic and Biomolecular Chemistry, 2003 , vol. 1, # 17 p. 3015 - 3023]
Synthetic and structural studies on 1, 2, 4-dithiazolidine-3, 5-dione derivatives
[Wood, Mark E.; Cane-Honeysett, Daniel J.; Dowle, Michael D.; Coles, Simon J.; Hursthouse, Michael B. Organic and Biomolecular Chemistry, 2003 , vol. 1, # 17 p. 3015 - 3023]