325479-39-8

Basic information

• Product Name: (3aS,4R,7aS)-6-(tert-butyldimethylsilyloxy)-3a,4,7,7a-tetrahydro-2-phenyl-4-[(R)-4-phenyl-2-oxazolidinon-3-yl]-1H-isoindole-1,3-(2H)-dione
• Synonyms: (3aS,4R,7aS)-6-(tert-butyldimethylsilyloxy)-3a,4,7,7a-tetrahydro-2-phenyl-4-[(R)-4-phenyl-2-oxazolidinon-3-yl]-1H-isoindole-1,3-(2H)-dione
• CAS NO: 325479-39-8
• Molecular Weight: 518.685
• Mol File: 325479-39-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (3aS,4R,7aS)-6-(tert-butyldimethylsilyloxy)-3a,4,7,7a-tetrahydro-2-phenyl-4-[(R)-4-phenyl-2-oxazolidinon-3-yl]-1H-isoindole-1,3-(2H)-dione(CAS DataBase Reference)
• NIST Chemistry Reference: (3aS,4R,7aS)-6-(tert-butyldimethylsilyloxy)-3a,4,7,7a-tetrahydro-2-phenyl-4-[(R)-4-phenyl-2-oxazolidinon-3-yl]-1H-isoindole-1,3-(2H)-dione(325479-39-8)
• EPA Substance Registry System: (3aS,4R,7aS)-6-(tert-butyldimethylsilyloxy)-3a,4,7,7a-tetrahydro-2-phenyl-4-[(R)-4-phenyl-2-oxazolidinon-3-yl]-1H-isoindole-1,3-(2H)-dione(325479-39-8)

Safety Data

• Hazardous Substances Data: 325479-39-8(Hazardous Substances Data)

Upstream product

• 941-69-5 N-phenyl-maleimide 
• 325479-30-9 (R,E)-3-(tert-butyldimethylsiloxy)-1-(4-phenyl-2-oxazolidinon-3-yl)-1,3-butadiene 
• 325479-27-4 (4R,1'E)-(-)-3-(3'-oxobut-1'-enyl)-4-phenyloxazolidin-2-one 
• 56613-80-0 D-2-phenylglycinol 
• 875-74-1 (R)-phenylglycine 
• 90319-52-1 (4R)-phenyl-2-oxazolidinone 

Downstream Products

• 325479-38-7 (3aS,7aR)-2-Phenyl-2,3,3a,4,5,7a-hexahydro-1H-isoindol-5-ol 
• 325479-36-5 (3aR-cis)-2,3,3a,4,5,7a-hexahydro-5-oxo-2-phenyl-1H-isoindole 

Relevant articles and documents

Racemic and asymmetric Diels-Alder reactions of 1-(2-oxazolidinon-3-yl)-3-siloxy-1,3-butadienes

Achiral and chiral 1-(2-oxazolidinon-3-yl)-3-siloxy-1,3-butadienes were prepared from readily available starting materials. Although more stable than the parent 1-amino-3-siloxy dienes, the 1-(2-oxazolidinon-3-yl)-3-siloxy-1,3-butadienes are still very reactive in Diels-Alder reactions, somewhat more than 1,3-dialkoxy-1,3-butadienes (e.g., Danishefsky's diene). The cycloadditions of the achiral and chiral dienes with several different dienophiles were examined. The reactions proceeded in good yield, with modest to high endo selectivity. The chiral dienes exhibited excellent facial selectivity in cycloadditions with α-substituted acroleins, maleic anhydride and N-phenylmaleimide. Upon reduction and hydrolysis of the cycloadducts, substituted cyclohexenones were obtained with ee's ranging from 22% to >98%.