80371-91-1

Upstream product

• 80348-96-5 (S)-2-Oxo-5-trityloxymethyl-tetrahydro-furan-3-carbaldehyde 
• 80348-97-6 (S)-2-Oxo-3-(3-oxo-butyl)-5-trityloxymethyl-tetrahydro-furan-3-carbaldehyde 

Downstream Products

• 112359-15-6 (R)-4-Benzyloxymethyl-4-((S)-2-benzyloxy-3-trityloxy-propyl)-cyclohex-2-enone 
• 112359-20-3 C₃₄H₄₆O₆ 
• 112388-15-5 Trimethyl-((4aS,8aS)-7-methyl-4a-trityloxymethyl-4a,5,6,8a-tetrahydro-2H-chromen-3-yloxy)-silane 
• 112359-18-9 (4aS,8aS)-4,7-Dimethyl-4a-trityloxymethyl-4a,5,6,8a-tetrahydro-4H-chromen-3-one 
• 112359-17-8 (4aS,8aS)-7-Methyl-4a-trityloxymethyl-4a,5,6,8a-tetrahydro-4H-chromen-3-one 
• 112359-24-7 (3S,4aS,8aS)-7-Methyl-4a-trityloxymethyl-3,4,4a,5,6,8a-hexahydro-2H-chromen-3-ol 
• 112359-19-0 (S)-1-[(R)-1-Hydroxymethyl-4-(tetrahydro-pyran-2-yloxy)-cyclohex-2-enyl]-3-(tetrahydro-pyran-2-yloxy)-propan-2-ol 
• 112359-16-7 (3S,4aS,8aS)-3-Benzyloxy-4a-benzyloxymethyl-7-methyl-3,4,4a,5,6,8a-hexahydro-2H-chromene 

Relevant academic research and scientific papers

HIGHLY STEREOSELECTIVE CONSTRUCTION OF CHIRAL QUATERNARY CARBON: ASYMMETRIC SYNTHESIS OF β,β-DISUBSTITUTED γ-BUTYROLACTONES

Asymmetric synthesis of β,β-disubstituted γ-butyrolactones was carried out in highly stereoselective and predictable way, by means of sequential dialkylation of (S)-γ-trityloxymethyl-γ-butyrolactone followed by lactone carbonyl transposition.Application t