103563-35-5

Upstream product

• 103563-33-3 (S)-(Z)-6-<(benzyloxy)methoxy>-2-hydroxy-4-(trimethylsilyl)-4-hexen-3-one 
• 103590-65-4 ((E)-3-Benzyloxymethoxy-1-bromo-propenyl)-trimethyl-silane 
• 96011-46-0 3-(benzyloxymethoxy)prop-1-yne 
• 3587-60-8 Benzyloxymethyl chloride 
• 103563-34-4 Methanesulfonic acid (Z)-(S)-5-benzyloxymethoxy-1-methyl-2-oxo-3-trimethylsilanyl-pent-3-enyl ester 

Downstream Products

• 103563-54-8 (3R,4S)-(E)-7-<(benzyloxy)methoxy>-4-methyl-5-hepten-3-ol 
• 103563-52-6 (3R,4R)-(Z)-7-<(benzyloxy)methoxy>-4-methyl-5-(trimethylsilyl)-5-hepten-3-ol 
• 103563-76-4 Phenoxy-acetic acid (E)-(1R,2S)-1-ethyl-2-methyl-5-oxo-pent-3-enyl ester 
• 103563-75-3 Phenoxy-acetic acid (E)-(1R,2S)-1-ethyl-5-hydroxy-2-methyl-pent-3-enyl ester 
• 103563-42-4 (4S,5S,6S)-(E)-9-<(benzyloxy)methoxy>-4,6-dimethyl-7-nonen-5-olide 
• 79495-87-7 protomycinolide IV 
• 103563-41-3 (E)-(3S,4S,5S)-8-Benzyloxymethoxy-1-[1,3]dithian-2-ylidene-3,5-dimethyl-oct-6-en-4-ol 
• 103843-96-5 (2S,3S)-2-<(S)-(E)-4-<(benzyloxy)methoxy>-1-methyl-2-buten-1-yl>-1-oxa-7,11-dithiaspiro<5.5>undecane 
• 103563-67-3 (Z)-(3S,4S,5R)-8-Benzyloxymethoxy-3,5-dimethyl-4-(tetrahydro-pyran-2-yloxy)-6-trimethylsilanyl-oct-6-en-1-ol 
• 103590-67-6 [(2R,3S,4S)-1-[2-Benzyloxymethoxy-eth-(Z)-ylidene]-2,4-dimethyl-3-(tetrahydro-pyran-2-yloxy)-hex-5-enyl]-trimethyl-silane 
• 103563-39-9 (Z)-(3S,4S,5R)-8-Benzyloxymethoxy-1-[1,3]dithian-2-ylidene-3,5-dimethyl-6-trimethylsilanyl-oct-6-en-4-ol 
• 103664-64-8 (3S,5S,6S)-6-((E)-(S)-4-Benzyloxymethoxy-1-methyl-but-2-enyl)-3,5-dimethyl-tetrahydro-pyran-2-one 
• 103563-43-5 (3R,5S,6S)-6-((E)-(S)-4-Benzyloxymethoxy-1-methyl-but-2-enyl)-3,5-dimethyl-tetrahydro-pyran-2-one 
• 103664-63-7 (Z)-(3R,4R,5R)-8-Benzyloxymethoxy-3,5-dimethyl-6-trimethylsilanyl-octa-1,6-dien-4-ol 

Relevant academic research and scientific papers

HIGHLY STEREOSELECTIVE APPROACH TO CHIRAL BUILDING BLOCK POSSESSING THREE CONTIGUOUS ASYMMETRIC CENTERS. PREPARATION OF FOUR POSSIBLE DIASTEREOMERS OF β,β'-DIMETHYL-BIS-HOMOALLYLIC ALCOHOL DERIVATIVE

All four diastereomers of chiral alcohol 2 with three contiguous chiral centers were stereoselectively prepared via diastereoselective addition of nucleophiles (crotyl metal or H(1-)) to α-methyl-β,γ-unsaturated carbonyl compounds 1.