Click chemistry inspired synthesis of ferrocene amino acids and other derivatives
This work reports the synthesis of a wide range of ferrocenyl-amino acids and other derivatives in excellent yield. Diverse amino acid containing azides were synthesized and ligated to ferrocene employing click reaction to access ferrocenyl amino acids. Chiral alcohols, esters, diols, amines containing azido group were tagged to ferrocene via click reaction to generate ferrocene derived chiral derivatives. A novel strategy for direct incorporation of ferrocene into a peptide and a new route to 1, 1′disubstituted ferrocene amino acid derivative are reported.
Sai Sudhir,Phani Kumar,Chandrasekaran
scheme or table
p. 1327 - 1334
(2010/03/30)
Facile entry into triazole fused heterocycles via sulfamidate derived azido-alkynes
(Chemical Equation Presented) Direct synthesis of condensed triazoles from diverse sulfamidates by ring opening of sulfamidates with sodium azide followed by one-pot propargylation and cycloaddition furnished title compounds. The methodology in general ha
Sudhir, V. Sai,Kumar, N. Y. Phani,Baig, R. B. Nasir,Chandrasekaran, Srinivasan
supporting information; experimental part
p. 7588 - 7591
(2010/01/16)
Application of the Mitsunobu Reaction for the Preparation of (L)-2,3-Diaminopropionic Acid from (L)-Serine.
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Golding, Bernard T.,Howes, Colin
p. 101 - 110
(2007/10/02)
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