942292-92-4

Upstream product

• 502690-34-8 (S)-1-[[(2R,4R,6R)-2-phenyl-6-(4-phenylbutyl)-1,3-dioxan-4-yl]methyl]-3-butenyl 2-propenoate 
• 36884-28-3 5-phenyl-1-pentanal 
• 814-68-6 acryloyl chloride 
• 821785-90-4 (R)-8-phenyloct-1-en-4-ol 
• 502690-44-0 (6R)-5,6-dihydro-6-[[(2R,4R,6R)-2-phenyl-6-(4-phenylbutyl)-1,3-dioxan-4-yl]methyl]-2H-pyran-2-one 

Relevant academic research and scientific papers

Biology-oriented synthesis of stereochemically diverse natural-product- derived compound collections by iterative allylations on a solid support

A strategy aiming at the introduction of stereocenters into polymer-bound natural-product-derived and -inspired compound collections is presented. Treatment of immobilized aldehydes with Brown's pinene-derived allylboranes results in the stereoselective f

Strategy for Enantio- and Diastereoselective Syntheses of All Possible Stereoisomers of 1,3-Polyol Arrays Based on a Highly Catalyst-Controlled Epoxidation of α,β-Unsaturated Morpholinyl Amides: Application to Natural Product Synthesis

We describe a new strategy for enantio- and diastereoselective syntheses of all possible stereoisomers of 1,3-polyol arrays. This strategy relies on a highly catalyst-controlled epoxidation of α,β-unsaturated morpholinyl amides promoted by the Sm-BINOL-Ph

Catalytic asymmetric synthesis of both syn- and anti-3,5-dihydroxy esters: application to 1,3-polyol/alpha-pyrone natural product synthesis.

[reaction: see text] We describe a catalytic asymmetric synthesis of both syn- and anti-3,5-dihydroxy esters. The method relies upon catalytic asymmetric epoxidation of alpha,beta-unsaturated imidazolides and amides, using lanthanide-BINOL complexes, and