New base??labile amino??protective groups for peptide synthesis

CGJ Verhart, GI Tesser

Index: Verhart, C. G. J.; Tesser, G. I. Recueil des Travaux Chimiques des Pays-Bas, 1988 , vol. 107, p. 621 - 626

Full Text: HTML

Citation Number: 38

Abstract

Recueil des Travaux Chimiques des Pays-Bas, 10711 1, November 1988 ... New base-labile amino-protective groups for peptide synthesis ... Laboratory of Organic Chemistry, Catholic University, Toernooiveld, 6525 ED Nijmegen, The Netherlands (Received May loth, 1988) ... Abstract. Modification of the methyl group in 2-(methylsulphony1)ethanol gave alcohols which could be used to introduce amino-protective groups of the urethane type, which are labile ...

Related Articles:

Ligand-coupling through σ-sulfurane formed on treatment of sulfilimines with hydride

[Kim, Kyoung Soo; Jung, In Bae; Kim, Yong Hae; Oae, Shigeru Tetrahedron Letters, 1989 , vol. 30, # 9 p. 1087 - 1090]

Ionic Liquids—Promoted S-Methylation of Thiols Utilizing Dimethyl Carbonate

[Xie, Jiangang; Wu, Chengyao; Christopher, Branford White; Quan, Jing; Zhu, Limin Phosphorus, Sulfur and Silicon and the Related Elements, 2011 , vol. 186, # 1 p. 31 - 37]

Alkyl??and Arylthiolation of Aryl Halides Catalyzed by Fluorinated Bis??Imino??Nickel NNN Pincer Complexes [NiCl2 {C5H3N??2, 6??(CHNArf) 2}]

[Baldovino-Pantaleon, Oscar; Hernandez-Ortega, Simon; Morales-Morales, David Advanced Synthesis and Catalysis, 2006 , vol. 348, # 1-2 p. 236 - 242]

Rhodium-Catalyzed Cleavage Reaction of Aryl Methyl Ethers with Thioesters

[Organic Letters, , vol. 14, # 3 p. 855 - 857]

Rhodium-Catalyzed Cleavage Reaction of Aryl Methyl Ethers with Thioesters

[Organic Letters, , vol. 14, # 3 p. 855 - 857]

More Articles...