(3R,8aS)-6-(benzyloxycarbonyl)-8a-(3-butenyl)-5-oxo-3-phenyl-6-(phenylselenyl)-2,3,6,7,8,8a-hexahydro-5H-oxazolo[3,2-a]pyridine

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Chemical Name:(3R,8aS)-6-(benzyloxycarbonyl)-8a-(3-butenyl)-5-oxo-3-phenyl-6-(phenylselenyl)-2,3,6,7,8,8a-hexahydro-5H-oxazolo[3,2-a]pyridine
CAS No.:1049705-26-1
Molecular Formula:C₃₁H₃₁NO₄Se
Molecular Weight:560.551
Hs Code.:

Synonyms:(3R,8aS)-6-(benzyloxycarbonyl)-8a-(3-butenyl)-5-oxo-3-phenyl-6-(phenylselenyl)-2,3,6,7,8,8a-hexahydro-5H-oxazolo[3,2-a]pyridine

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Chemical Property of (3R,8aS)-6-(benzyloxycarbonyl)-8a-(3-butenyl)-5-oxo-3-phenyl-6-(phenylselenyl)-2,3,6,7,8,8a-hexahydro-5H-oxazolo[3,2-a]pyridine

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Technology Process of (3R,8aS)-6-(benzyloxycarbonyl)-8a-(3-butenyl)-5-oxo-3-phenyl-6-(phenylselenyl)-2,3,6,7,8,8a-hexahydro-5H-oxazolo[3,2-a]pyridine

There total 1 articles about (3R,8aS)-6-(benzyloxycarbonyl)-8a-(3-butenyl)-5-oxo-3-phenyl-6-(phenylselenyl)-2,3,6,7,8,8a-hexahydro-5H-oxazolo[3,2-a]pyridine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 88.0%

: 5707-04-0
Phenylselenyl chloride

: (3R)-8a-(3-butenyl)-5-oxo-3-phenyl-2,3,6,7,8,8a-hexahydro-5H-oxazolo[3,2-a]pyridine

: 501-53-1,94274-21-2
benzyl chloroformate

: 1049705-26-1
(3R,8aS)-6-(benzyloxycarbonyl)-8a-(3-butenyl)-5-oxo-3-phenyl-6-(phenylselenyl)-2,3,6,7,8,8a-hexahydro-5H-oxazolo[3,2-a]pyridine

Guidance literature:: (3R)-8a-(3-butenyl)-5-oxo-3-phenyl-2,3,6,7,8,8a-hexahydro-5H-oxazolo[3,2-a]pyridine; With lithium hexamethyldisilazane; In tetrahydrofuran; at -78 ℃; for 1.5h;

benzyl chloroformate; In tetrahydrofuran; at -78 ℃; for 1h;

Phenylselenyl chloride; In tetrahydrofuran; at -78 ℃; for 1h; Further stages.;
DOI:10.1021/jo801172b