106930-36-3

Upstream product

• 75-36-5 acetyl chloride 
• 106930-33-0 (2S,3S,4S)-3,5-Dimethyl-2-phenyl-3,4-dihydro-2H-pyran-4-ol 
• 108-05-4 vinyl acetate 
• 138512-14-8 (2S,3S,4S)-3,5-Dimethyl-2-phenyl-3,4-dihydro-2H-pyran-4-ol 
• 138512-12-6 (2S,3R,4S)-3,5-Dimethyl-2-phenyl-3,4-dihydro-2H-pyran-4-ol 

Downstream Products

• 106930-44-3 (3S,3aS,5R,6S,7R,7aR)-3,6,7a-Trimethyl-5-phenyl-7-phenylselanyl-hexahydro-furo[3,2-b]pyran 
• 106930-44-3 (3R,3aS,5R,6S,7R,7aR)-3,6,7a-Trimethyl-5-phenyl-7-phenylselanyl-hexahydro-furo[3,2-b]pyran 

Relevant academic research and scientific papers

A route to artificial glycoconjugates and oligosaccharides via enzymatically resolved glycals: Dramatic effects of the handedness of the sugar domain upon the properties of an anthracycline drug

Racemic, fully synthetic glycals of considerable structural variety may be kinetically resolved via enzymatically mediated transesterification using Lipase PS-30 from Pseudomonas cepacia as catalyst and vinyl acetate as acyl donor. This methodology provid

Enzymatic resolution of racemic glycals: An application of the wong acylation method

Kinetic resolution of racemic, fully synthetic, artificial glycals bearing a free hydroxyl group at C3 was accomplished through the more rapid acylation of the 'D'-antipode with vinyl acetate as acyl donor and Lipase PS-30 from Pseudomonas cepa

A Concise and Stereoselective Route to the Predominant Stereochemical Pattern of the Tetrahydropyranoid Antibiotics: An Application to Indanomycin

The reactions of (E)- and (Z)-crotylsilanes of the type R3Si-CH2-CH=CH-CH3 with activated glycal derivatives in the presence of BF3 etherate have been examined.In all cases, the reactions were regiospecific, resulting in incorporation of a 3-methylprop-1-