1351992-98-7

Upstream product

• 16387-61-4 6-phenylhexanal 

Downstream Products

• 934473-34-4 (2R,4R)-4-(tert-butyldimethylsilyloxy)-8-phenyloctane-1,2-diol 
• 1149764-67-9 (4S,6R)-6-(tert-butyldimethylsilanyloxy)-10-phenyldec-1-en-4-ol 
• 1149764-68-0 (4S,6R)-6-(tert-butyldimethyl silanyloxy)-10-phenyldec-1-en-4-yl acrylate 
• 1149764-69-1 (6S)-5,6-dihydro-6-[(2R)-2-(tert-butyldimethyl silanyloxy)-6-phenylhexyl]-2H-pyran-2-one 
• 1160697-63-1 tert-butyldimethyl((R)-1-((R)-oxiran-2-yl)-6-phenylhexan-2-yloxy)silane 
• 1351993-00-4 (4S,6R)-10-phenyldec-1-ene-4,6-diol 
• 1351993-11-7 C₂₀H₃₄O₂Si 
• 1351993-12-8 C₂₆H₄₁NO₃Si 
• 397871-02-2 (6S)-5,6-dihydro-6-[(2R)-2-hydroxy-6-phenylhexyl]-2H-pyran-2-one 
• 1351992-99-8 (R)-methyl 4-(tert-butyldimethylsilyloxy)-8-phenyloctanoate 

Relevant academic research and scientific papers

An organocatalytic route to the synthesis of (6S)-5,6-dihydro-6-[(2R)-2- hydroxy-6-phenylhexyl]-2H-pyran-2-one and ravensara lactones

An organocatalytic enantioselective synthesis of the title compounds has been achieved. The stereogenic centers were generated by the iterative use of proline catalyzed α-aminoxylations and HWE olefination of aldehydes while the lactone ring was construct