1454313-46-2

Basic information

• Product Name: (3S,4aR,6R,7R,8S)-3-allyl-6,7-bis(benzyloxy)-8-(benzyloxymethyl)hexahydropyrido[1,2-c][1,3]oxazin-1(3H)-one
• Synonyms: (3S,4aR,6R,7R,8S)-3-allyl-6,7-bis(benzyloxy)-8-(benzyloxymethyl)hexahydropyrido[1,2-c][1,3]oxazin-1(3H)-one
• CAS NO: 1454313-46-2
• Molecular Weight: 527.66
• Mol File: 1454313-46-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (3S,4aR,6R,7R,8S)-3-allyl-6,7-bis(benzyloxy)-8-(benzyloxymethyl)hexahydropyrido[1,2-c][1,3]oxazin-1(3H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: (3S,4aR,6R,7R,8S)-3-allyl-6,7-bis(benzyloxy)-8-(benzyloxymethyl)hexahydropyrido[1,2-c][1,3]oxazin-1(3H)-one(1454313-46-2)
• EPA Substance Registry System: (3S,4aR,6R,7R,8S)-3-allyl-6,7-bis(benzyloxy)-8-(benzyloxymethyl)hexahydropyrido[1,2-c][1,3]oxazin-1(3H)-one(1454313-46-2)

Safety Data

• Hazardous Substances Data: 1454313-46-2(Hazardous Substances Data)

Upstream product

• 1454313-37-1 benzyl (2S,3R,4R,6R)-6-Allyl-3,4-bis(benzyloxy)-2-(benzyloxymethyl)piperidine-1-carboxylate 
• 1454313-36-0 benzyl (4R,5R,6S)-3,4-bis(benzyloxy)-2-(benzyloxymethyl)-6-oxopiperidine-1-carboxylate 
• 1454313-35-9 (4R,5R,6S)-4,5-bis(benzyloxy)-6-(benzyloxymethyl)piperidin-2-one 
• 475630-58-1 methyl (3R,4R,5R)-3,4,6-tris(benzyloxy)-5-hydroxyhexanoate 
• 79999-46-5 (4R,5S,6R)-4,5-bis(benzyloxy)-6-(benzyloxymethyl)tetrahydro-2H-pyran-2-one 
• 55628-54-1 3,4,6-tri-O-benzyl-D-glucal 
• 1454313-45-1 benzyl (2S,3R,4R,6R)-3,4-bis(benzyloxy)-2-(benzyloxymethyl)-6-[(2S)-2-hydroxypent-4-enyl]piperidine-1-carboxylate 

Downstream Products

• 1454313-47-3 (3S,4aR,6R,7R,8S)-6,7-bis(benzyloxy)-8-(benzyloxymethyl)-3-(dec-2-en-1-yl)hexahydropyrido[1,2-c][1,3]oxazin-1(3H)-one 
• 1454313-48-4 (3S,4aR,6R,7R,8S)-6,7-bis(benzyloxy)-8-(benzyloxymethyl)-3-(non-2-en-1-yl)hexahydropyrido[1,2-c][1,3]oxazin-1(3H)-one 
• 1454313-49-5 (3S,4aR,6R,7R,8S)-6,7-bis(benzyloxy)-8-(benzyloxymethyl)-3-(undec-2-en-1-yl)hexahydropyrido[1,2-c][1,3]oxazin-1(3H)-one 

Relevant articles and documents

Stereoselective total synthesis of (-)-batzellasides a, b, and c

Total synthesis of (-)-L-batzellasides A, B, and C has been achieved in 13 steps from known lactone 2 in 12.6, 13.2, and 13.8 % overall yields, respectively. The key steps in this synthesis were the stereoselective introduction of an allyl group at the C1