765940-97-4

Basic information

• Product Name: (R)-(+)-1-phenylbut-3-enyl acrylate
• Synonyms: (R)-(+)-1-phenylbut-3-enyl acrylate
• CAS NO: 765940-97-4
• Molecular Weight: 202.253
• Mol File: 765940-97-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (R)-(+)-1-phenylbut-3-enyl acrylate(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-(+)-1-phenylbut-3-enyl acrylate(765940-97-4)
• EPA Substance Registry System: (R)-(+)-1-phenylbut-3-enyl acrylate(765940-97-4)

Safety Data

• Hazardous Substances Data: 765940-97-4(Hazardous Substances Data)

Upstream product

• 77118-87-7 (S)-1-Phenyl-3-buten-1-ol 
• 100-52-7 benzaldehyde 
• 80735-94-0 1-Phenyl-3-buten-1-ol 
• 181227-42-9 (+)-(R)-1-phenylbut-3-en-1-yl acetate 
• 85551-57-1 (R)-1-Phenylbut-3-en-1-ol 
• 814-68-6 acryloyl chloride 

Downstream Products

• 765940-99-6 (R)-(+)-5,6-dihydro-6-phenylpyran-2-one 
• 765941-01-3 (3S,4S,6R)-3,4-dihydroxy-6-phenyltetrahydropyran-2-one 
• 112607-33-7 (+)-(R)-δ-(phenyl)-δ-valerolactone 

Relevant articles and documents

Dynamic kinetic resolution of homoallylic alcohols: Application to the synthesis of enantiomerically pure 5,6-dihydropyran-2-ones and δ-lactones

Dynamic kinetic resolution of various homoallylic alcohols with the use of Candida antarctica lipase B and ruthenium catalyst 2 afforded homoallylic acetates in high yields and with high enantioselectivity. These enantiopure acetates were further transfor

Diastereoselective dihydroxylation and regioselective deoxygenation of dihydropyranones: A novel protocol for the stereoselective synthesis of C 1-C8 and C15-C21 subunits of (+)-discodermolide

Diastereoselective dihydroxylation of dihydropyranones and subsequent regioselective α-deoxygenation provides 1,3-trans-β-hydroxy-6- lactones stereoselectively. This protocol has been applied for the synthesis of C1-C8 and C15-C21 subunits of (+)-discodermolide.