124662-67-5

Upstream product

• 124662-63-1 (S)-5-Benzyloxy-4-tert-butyldimethylsiloxy-1-pentyne 
• 124752-65-4 (Z)-(S)-6-Benzyloxy-5-hydroxy-hex-2-enoic acid 
• 124662-62-0 (S)-6-Benzyloxy-5-hydroxy-hex-2-ynoic acid 
• 124662-61-9 (S)-5-Benzyloxy-4-hydroxy-1-pentyne 
• 124662-64-2 Methyl (S)-6-benzyloxy-5-tert-butyldimethylsiloxy-2-hexynoate 
• 124662-65-3 Methyl (S,Z)-6-benzyloxy-5-tert-butyldimethylsiloxy-2-hexenoate 
• 2930-05-4 (S)-benzyl glycidyl ether 
• 197520-74-4 ethyl (5S)-6-(benzyloxy)-5-hydroxyhex-2-ynoate 
• 197520-75-5 (Z)-(S)-6-Benzyloxy-5-hydroxy-hex-2-enoic acid ethyl ester 
• 291506-91-7 (S)-1-(benzyloxy)-4-penten-2-yl p-nitrobenzoate 
• 291506-87-1 (R)-1-(benzyloxy)-4-penten-2-yl acetate 
• 58931-16-1 (R)-1-benzyloxypent-4-en-2-ol 
• 58931-16-1 1-(benzyloxy)-4-penten-2-ol 
• 291506-84-8 (S)-1-(benzyloxy)-4-penten-2-ol acrylic ester 

Downstream Products

• 291506-89-3 (3R,5S)-6-benzyloxy-3,5-dihydroxyhexanoic acid isopropyl ester 
• 92757-18-1 (4R,6S)-6-(benzyloxy)methyl-4-hydroxy-tetrahydro-2-pyrone 

Relevant academic research and scientific papers

Asymmetric allylboration for the synthesis of β-hydroxy-δ-lactone unit of statin drug analogs

Acrylic esters of homoallylic alcohols prepared in 92-96% ee via the asymmetric allylboration of appropriate aldehydes with B-allyldiisopinocampheylborane, upon ring-closing metathesis in the presence of 10mol% of Grabbs' catalyst provided the correspondi

A Unified Procedure for Diastereo- and Enantiocontrolled Construction of Compactin Lactone and Calcitriol Enyne

A unified diastereo- and enantiocontrolled entry into compactin lactone, an essential structural moiety for the biological activity of compactin, and calcitriol enyne, an A-ring precursor of calcitriol, has been developed by use of the same stereocontrol