439665-53-9Relevant academic research and scientific papers
Bamford-Stevens reaction assisted synthesis of styrene C-glycosides
Singh, Balram,Kumar, Sandeep,Maity, Jyotirmoy,Roy, Indrajit,Prasad, Ashok K.
, p. 1906 - 1912 (2019)
Modification of carbohydrates and their analogs is hindered due to multi-step synthetic methodologies involving selective protection and deprotection of multiple hydroxyl groups present in the molecule. A highly efficient route for the synthesis of 1-phen
Synthesis of β-C-Glycopyranosyl Aldehydes and 2,6-Anhydro-heptitols
Khatri, Vinod,Kumar, Amit,Singh, Balram,Malhotra, Shashwat,Prasad, Ashok K.
, p. 11169 - 11174 (2015/11/18)
A convenient route has been developed for the diastereoselective synthesis of β-C-glycopyranosyl aldehydes from d-glucose, d-mannose, and d-galactose. The key step in the synthesis of C-glycosyl aldehydes is the aryl driven reductive dehydration on 1-phen
Microwave-assisted efficient synthesis of aryl ketone β-C-glycosides from unprotected aldoses
Feng, Weiwei,Fang, Zhijie,Yang, Jingmei,Zheng, Baohui,Jiang, Yuhua
scheme or table, p. 352 - 356 (2011/03/18)
Condensation between unprotected aldoses and dibenzoylmethane catalyzed by NaHCO3 in the cosolvents EtOH and H2O (4:1) under microwave irradiation gave aryl ketone β-C-glycosides 6b-i in higher yields (from 50% with C-riboside 6g up
