146566-38-3

Upstream product

• 146514-61-6 (2S,3R,4S,5S) 5-<(t-butyldimethylsilyl)oxy>-2,3,4-tris(benzyloxy)-1-<(trimethylsilyl)oxy>-1,6-cyclohexene 
• 159701-15-2 (1R,2S,3R,4S,5S,6S) 5-<(t-butyldimethylsilyl)oxy>-2,3,4-tris(benzyloxy)-1-<(trimethylsilyl)oxy>bicyclo<4.1.0>heptane 
• 146514-64-9 (2S,3R,4S,5S) 5-<(t-butyldimethylsilyl)oxy>-2,3,4-tris(benzyloxy) cyclohept-6,7-en-1-one 
• 87326-88-3 methyl 6-deoxy-6-iodo-2,3-bis-O-(phenylmethyl)-α-D-glucopyranoside 
• 85716-44-5 methyl 2,3,4-tri-O-benzyl-α-d-xylo-hex-5-enopyranoside 
• 131289-28-6 (2S,3R,4R,5S) 5-<(t-butyldimethylsilyl)oxy>-2,3,4-tris(benzyloxy) cyclohexane-1-one 
• 100-39-0 benzyl bromide 
• 85716-45-6 1L-(2,4,5/3)-2,3,4-Tri-O-benzyl-2,3,4,5-tetrahydroxy-1-cyclohexanon 
• 69739-34-0 t-butyldimethylsiyl triflate 
• 146514-60-5 (2S,3R,4S,5S) 5-<(t-butyldimethylsilyl)oxy>-2,3,4-tris(benzyloxy) cycloheptane-1-one 

Relevant academic research and scientific papers

Enantioselective syntheses of polyhydroxylated nortropane derivatives: Total synthesis of (+) and (-)-calystegine B2

(+) and (-)-Calystegine B2 were prepared from D-Glucose via Ferrier reaction followed by regiospecific ring enlargement of a polysubstituted cyclohexanone and intramolecular cyclisation of 4-aminocycloheptanone.