852609-51-9Relevant academic research and scientific papers
Chemoselective deprotection of cyclic N,O-aminals using catalytic bismuth(III) bromide in acetonitrile
Cong, Xin,Hu, Fang,Liu, Ke-Gang,Liao, Qing-Jiang,Yao, Zhu-Jun
, p. 4514 - 4516 (2005)
Cyclic N,O-aminals can be chemoselectively and efficiently deprotected using a catalytic amount of bismuth(III) bromide in acetonitrile at room temperature. This selectivity was also achieved in the presence of terminal O,O-acetal functionality. The susce
Parallel synthesis of individual shikimic acid-like molecules using a mixture-operation strategy and ring-closing enyne metathesis
Hu, Fang,Zhang, Yan-Hong,Yao, Zhu-Jun
, p. 3511 - 3515 (2008/02/06)
Three new diastereomeric shikimic acid analogues (4-amino-3,5-dihydroxyl-cyclohex-1-en-carboxylic acids, 16) bearing a C-4 amino group were synthesized in parallel by a mixture-operation protocol. Ring-closing enyne metathesis (RCEYM) under ethylene atmos
