135799-73-4

Upstream product

• 67-56-1 methanol 
• 135799-72-3 (2R,4R,5S,6R,7R)-9-Benzyloxy-7-(tert-butyl-dimethyl-silanyloxy)-4-((E)-2-methoxymethoxy-vinyl)-2,6-dimethyl-nonane-1,5-diol 
• 138152-94-0 (2S,3R)-2-<(1R,2R)-4-(Benzyloxy)-2-<(tert-butyldimethylsilyl)oxy>-1-methylbutyl>-3-<(2R)-3-<<(p-methoxybenzyl)oxy>methoxy>-2-methylpropyl>-5-methoxy-1,2,3,4-tetrahydrofuran 
• 80879-46-5 {(1R,2R)-1-(2-Benzyloxy-ethyl)-2-[(2S,3R)-5-methoxy-3-(2-methyl-allyl)-tetrahydro-furan-2-yl]-propoxy}-tert-butyl-dimethyl-silane 
• 80879-45-4 (4R,5S)-5-((1S,2R)-4-Benzyloxy-2-hydroxy-1-methyl-butyl)-4-(2-methyl-allyl)-dihydro-furan-2-one 
• 4799-68-2 3-benzyloxypropan-1-ol 
• 138152-94-0 ((1R,2S)-1-(2-Benzyloxy-ethyl)-2-{(2R,3R)-5-methoxy-3-[(R)-3-(4-methoxy-benzyloxymethoxy)-2-methyl-propyl]-tetrahydro-furan-2-yl}-propoxy)-tert-butyl-dimethyl-silane 
• 69739-34-0 t-butyldimethylsiyl triflate 
• 19790-60-4 3-Benzyloxypropanal 
• 95531-98-9 (Z)-5-(Benzyloxy)-2-methyl-2-penten-1-ol 
• 80879-44-3 3-[(4S,5S,6R)-6-(2-Benzyloxy-ethyl)-2,2,5-trimethyl-[1,3]dioxan-4-yl]-5-methyl-hex-5-enoic acid ethyl ester 
• 138152-91-7 Toluene-4-sulfonic acid (2R,4R)-2-[(4R,5R,6R)-6-(2-benzyloxy-ethyl)-2,2,5-trimethyl-[1,3]dioxan-4-yl]-5-(4-methoxy-benzyloxymethoxy)-4-methyl-pentyl ester 
• 138152-89-3 [(2R,4R)-2-[(4R,6R)-6-(2-Benzyloxy-ethyl)-2,2-dimethyl-5-methylene-[1,3]dioxan-4-yl]-5-(4-methoxy-benzyloxymethoxy)-4-methyl-pentyloxy]-tert-butyl-dimethyl-silane 
• 138152-86-0 (2R,4R,5R,6R,7R)-9-(Benzyloxy)-4-<<(tert-butyldimethylsilyl)oxy>methyl>-5,6-epoxy-1-<<(p-methoxybenzyl)oxy>methoxy>-2,6-dimethyl-7-nonanol 

Downstream Products

• 80879-48-7 ((R)-4-{(2S,3R)-2-[(1R,2R)-4-Benzyloxy-2-(tert-butyl-dimethyl-silanyloxy)-1-methyl-butyl]-5-methoxy-tetrahydro-furan-3-yl}-3-methyl-2-oxo-butyl)-phosphonic acid dimethyl ester 
• 80879-47-6 (R)-3-{(2S,3R)-2-[(1R,2R)-4-Benzyloxy-2-(tert-butyl-dimethyl-silanyloxy)-1-methyl-butyl]-5-methoxy-tetrahydro-furan-3-yl}-2-methyl-propionaldehyde 

Relevant academic research and scientific papers

Highly Stereoselective SE' Additions of α-Alkoxy Allylstannanes to Chiral Aldehydes. Synthesis of a C-1-C-9 Subunit of Tylonolide

The racemic α-alkoxy allylic stannane RS4 adds to the 2S aldehyde 24 to afford the homoaldol adduct 25 (45percent) derived exclusively from the S enantiomer S4 along with isomerized (R)-γ-alkoxy allylstannane 26 of >80percentee (50percent) and unreacted a