485321-74-2

Upstream product

• 485321-87-7 ((4R,6S)-2,2-Dimethyl-6-phenethyl-[1,3]dioxan-4-yl)-acetaldehyde 
• 485321-82-2 tert-Butyl-[2-((4S,6S)-2,2-dimethyl-6-phenethyl-[1,3]dioxan-4-yl)-ethoxy]-diphenyl-silane 
• 502690-42-8 ethyl (3R,5S)-3,5-isopropylidenedioxy-7-phenylheptanoate 
• 745058-36-0 tert-butyl-{2-[(4S,6S)-2,2-dimethyl-6-phenethyl-[1,3]dioxan-4-yl]ethoxy}-dimethylsilane 
• 17376-04-4 2-phenethyl iodide 
• 745058-30-4 (4S,6S)-4-[2-(tert-butyldimethylsilanyloxy)ethyl]-2,2-dimethyl-6-phenethyl-[1,3]dioxan-5-one 
• 745058-28-0 {(4S,6S)-4-[2-(tert-butyldimethylsilanyloxy)ethyl]-2,2-dimethyl-6-phenethyl-[1,3]dioxan-(5E)-ylidene}-[(S)-2-methoxymethylpyrrolidin-1-yl]-amine 
• 485321-73-1 (R)-6-[(E)-3-((4S,6S)-2,2-Dimethyl-6-phenethyl-[1,3]dioxan-4-yl)-propenyl]-5,6-dihydro-pyran-2-one 
• 485321-81-1 (3S,5S)-1-(tert-Butyl-diphenyl-silanyloxy)-7-phenyl-heptane-3,5-diol 
• 485321-80-0 7-(tert-butyl-diphenyl-silanyloxy)-5-hydroxy-1-phenyl-heptan-3-one 
• 485321-79-7 4-(tert-butyl-diphenyl-silanyloxy)-1-(2-phenethyl-[1,3]dithian-2-yl)-butan-2-ol 

Downstream Products

• 485321-89-9 Methanesulfonic acid 2-((4S,6S)-2,2-dimethyl-6-phenethyl-[1,3]dioxan-4-yl)-ethyl ester 
• 485321-84-4 (4R,6S)-4-(2-Bromo-ethyl)-2,2-dimethyl-6-phenethyl-[1,3]dioxane 
• 745058-49-5 {(E)-(R)-1-allyl-4-[(4S,6S)-2,2-dimethyl-6-phenethyl-[1,3]dioxan-4-yl]-but-2-enyloxy}-tert-butyldimethylsilane 
• 548483-78-9 acrylic acid (E)-(R)-1-allyl-4-{(4S,6S)-2,2-dimethyl-6-phenethyl-[1,3]dioxan-4-yl}-but-2-enyl ester 
• 548483-77-8 (E)-(R)-7-((4S,6S)-2,2-Dimethyl-6-phenethyl-[1,3]dioxan-4-yl)-hepta-1,5-dien-4-ol 
• 485321-85-5 5-{2-[(4R,6S)-2,2-dimethyl-6-phenethyl-[1,3]dioxan-4-yl]-ethylsulfonyl}-1-phenyl-1H-tetrazole 
• 485321-90-2 5-{2-[(4R,6S)-2,2-dimethyl-6-phenethyl-[1,3]dioxan-4-yl]-ethylsulfanyl}-1-phenyl-1H-tetrazole 
• 485321-86-6 (4S,6S)-4-{(E)-3-[(2R,6R)-6-isopropoxy-3,6-dihydro-2H-pyran-2-yl]-allyl}-2,2-dimethyl-6-phenethyl-[1,3]dioxane 
• 745058-38-2 (4R,6S)-4-(2-iodoethyl)-2,2-dimethyl-6-phenethyl-[1,3]dioxane 

Relevant academic research and scientific papers

Efficient asymmetric syntheses of (+)-strictifolione

The asymmetric synthesis and a formal asymmetric synthesis of (+)-strictifolione are described. As key step in both approaches the Julia-Kocienski olefination to create an E-configured alkene was used. The anti-1,3-diol moiety was synthesized by employing

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

First total synthesis and determination of the absolute configuration of strictifolione, a new 6-(ω-phenylalkenyl)-5,6-dihydro-α-pyrone, isolated from Cryptocarya strictifolia

Starting from (S)-malic acid and (S)-glycidol, the first total synthesis of strictifolione, a new 6-(ω-phenylalkenyl)-5,6-dihydro-α-pyrone isolated from Cryptocarya strictifolia, was accomplished, which confirmed its structure including the absolute confi