710965-64-3Relevant academic research and scientific papers
Efficient synthesis of olinked glycoconjugates of amino acids from carbohydrate-derived donor-acceptor cyclopropanes
Kishore, Gade,Gautam, Vibha,Haveli, Shrutisagar Dattatraya,Chandrasekaran, Srinivasan
, p. 200 - 212 (2019/07/31)
- VV-Iodosuccinimide (NIS) mediated ring opening of carbohydrate-derived donor-acceptor cyclopropanes with free "CO2H" group of VV-protected L-amino acids at ambient conditions afforded iodo derivatives of glycosyl ester of L-amino acids. The iodides were
Synthesis of unnatural C-2 amino acid nucleosides using NIS-mediated ring opening of 1,2-cyclopropane carboxylated sugar derivatives
Haveli, Shrutisagar Dattatraya,Roy, Sudipta,Chandrasekaran, Srinivasan
scheme or table, p. 451 - 455 (2009/07/25)
We have developed a general and efficient method for the stereoselective construction of pyrimidine-based pyranosyl C-2 amino acid nucleosides using NIS-mediated ring opening of 1,2-cyclopropanated sugar derivatives. This methodology has been successfully
Efficient synthesis of fused perhydrofuro[2,3-b]pyrans (and furans) by ring opening of 1,2-cyclopropanated sugar derivatives
Haveli, Shrutisagar Dattatraya,Sridhar, Perali Ramu,Suguna, Perumal,Chandrasekaran, Srinivasan
, p. 1331 - 1334 (2008/01/01)
Figure presented An efficient method has been developed for the construction of fused perhydrofuro{2,3-b]pyrans by dlastereoselective ring opening of 1,2-cyclopropanated sugar derivatives. The methodology has been successfully applied to the synthesis of
Efficient methodology for the synthesis of 2-C-branched glyco-amino acids by ring opening of 1,2-cyclopropanecarboxylated sugars
Sridhar, Perali Ramu,Ashalu, K. Chinna,Chandrasekaran
, p. 1777 - 1779 (2007/10/03)
Matrix presented. An efficient methodology for the synthesis of 2-C-branched glyco-amino acid derivatives by diastereoselective ring opening of 1,2-cyclopropanecarboxylated sugars in good yields is reported.
