478286-86-1

Upstream product

• 100-39-0 benzyl bromide 
• 387821-78-5 22-hydroxy-6β-methoxy-3α,5α-cyclocholestane-16β,17α-diol 
• 7488-31-5 isoamyl lithium 

Downstream Products

• 478286-92-9 6β-methoxy-3α,5α-cyclocholestane-16β,17α,22-triol 16-O-{O-[3,4-di-O-triethylsilyl-2-O-(4-methoxybenzoyl)-β-D-xylopyranosyl]-(1->3)-2-O-acetyl-4-O-triethylsilyl-α-L-arabinopyranoside} 
• 478286-99-6 C₆₆H₁₁₂O₁₅Si₃ 
• 145075-81-6 3β,16β,17α-trihydroxycholest-5-en-22-one 16-O-{O-[2-O-(4-methoxybenzoyl)-β-D-xylopyranosyl]-(1->3)-2-O-acetyl-β-L-arabinopyranoside} 
• 478286-96-3 22-benzyloxy-6β-methoxy-3α,5α-cyclocholestane-16β,17α-diol 16-O-{O-[3,4-di-O-triethylsilyl-2-O-(4-methoxybenzoyl)-β-D-xylopyranosyl]-(1->3)-2-O-acetyl-4-O-triethylsilyl-α-L-arabinopyranoside} 

Relevant academic research and scientific papers

Synthesis of a cholestane glycoside OSW-1 with potent cytostatic activity.

The potent antitumor agent OSW-1 was synthesized from the protected aglycone in different ways. It was proven that direct glycosylation of the aglycone in its hemiketal form could be achieved, affording the protected OSW-1 in a moderate yield. Alternatively, regioselective protection of the triol obtained by reduction of the aglycone, followed by glycosylation, deprotection and oxidation yielded the same OSW-1 derivative. The third approach to this compound consisted of glycosylation of the previously described lactol [Morzycki, J. W.; Gryszkiewicz, A. Polish J. Chem. 2001, 75, 983-989], reaction of the resulting aldehyde with a Grignard reagent, and oxidation. OSW-1 obtained on removal of the protective groups was identical with the natural product.