Journal of the American Chemical Society

New Methods in Peptide Synthesis. II. Further Examples of the Use of the o-Nitrophenylsulfenyl Group for the Protection of Amino Groups1, 2

L Zervas, C Hamalidis

Index: Journal of the American Chemical Society, , vol. 87, p. 99 - 104

Full Text: HTML

Citation Number: 49

Abstract

... Chem. Soc., 85, 3660 (1963). (4) J. P. Greenstein and M. Winitz, "Chemistry of the Amino Acids," John Wiley and Sons, Inc., New York, N. Y., 1961. (5) Cf. ... J . , 55, 328 (1953). 102 Journal of the American Chemical Society 1 87:l 1 January 5, 1965 Page 5. Anal. Calcd. ...

Related Articles:

Palladium-catalyzed reaction of tributyltin hydride. Selective and very mild deprotection of allyl and allyloxycarbonyl derivatives of amino-acids.

[Guibe, F.; Dangles, O.; Balavoine, G. Tetrahedron Letters, 1986 , vol. 27, # 21 p. 2365 - 2368]

Improved Syntheses of Nε-Tert-butyloxycarbonyl-L-lysine and Nα-Benzyloxycarbonyl-Nε-tert-butyloxycarbonyl-I-lysine

[Synthetic Communications, , vol. 11, # 4 p. 303 - 314]

Thermal cleavage of the Fmoc protection group

[Hoeck, Stefan; Marti, Roger; Riedl, Rainer; Simeunovic, Marina Chimia, 2010 , vol. 64, # 3 p. 200 - 202]

Improved Syntheses of Nε-Tert-butyloxycarbonyl-L-lysine and Nα-Benzyloxycarbonyl-Nε-tert-butyloxycarbonyl-I-lysine

[Synthetic Communications, , vol. 11, # 4 p. 303 - 314]

Improved Syntheses of Nε-Tert-butyloxycarbonyl-L-lysine and Nα-Benzyloxycarbonyl-Nε-tert-butyloxycarbonyl-I-lysine

[Synthetic Communications, , vol. 11, # 4 p. 303 - 314]

More Articles...