549513-47-5

Upstream product

• 1125-88-8 benzaldehyde dimethyl acetal 
• 695177-30-1 (3S,5R)-3,5-Dihydroxy-6-((2S,4R,6S)-6-methyl-2-phenyl-[1,3]dioxan-4-yl)-hexanoic acid ethyl ester 
• 361521-37-1 (2S,4S,6S)-4-(2-hydroxypent-4-enyl)-2-methyl-6-phenyl-1,3-dioxane 
• 695177-27-6 2-((2S,4R,6S)-6-Methyl-2-phenyl-[1,3]dioxan-4-yl)-ethanol 
• 188924-70-1 ((2S,4S,6S)-6-Methyl-2-phenyl-[1,3]dioxan-4-yl)-acetaldehyde 
• 100-52-7 benzaldehyde 
• 549513-48-6 (R)-5-hydroxy-6-(6-methyl-2-phenyl-[1,3]dioxan-4-yl)-hex-2-enoic acid ethyl ester 
• 695177-09-4 4-[(2R,3S)-2,3-epoxy-4-[(2S,4R,6S)-6-methyl-2-phenyl-1,3-dioxan-4-yl]-1-oxobutyl]morpholine 
• 695177-08-3 4-[(E)-4-[(2S,4R,6S)-6-methyl-2-phenyl-1,3-dioxan-4-yl]-1-oxo-2-butenyl]morpholine 

Downstream Products

• 549513-49-7 6-(6-methyl-2-phenyl-[1,3]dioxan-4-ylmethyl)-2-phenyl-[1,3]dioxan-4-yl-acetaldehyde 
• 549513-50-0 4-[6-(6-methyl-2-phenyl-[1,3]dioxan-4-ylmethyl)-2-phenyl-[1,3]dioxan-4-yl]-but-2Z-enoic acid methyl ester 

Relevant academic research and scientific papers

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

Enantioselective syntheses of cryptocarya triacetate, Cryptocaryolone, and cryptocaryolone diacetate

(Matrix presented) The enantioselective syntheses of three natural products from Cryptocarya latifolia have been achieved in 13-15 steps from ethyl sorbate. The route relies upon an enantio- and regioselective Sharpless dihydroxylation and a palladium-cat