135799-65-4

Upstream product

• 19790-60-4 3-Benzyloxypropanal 
• 787552-67-4 (S)-4-benzyl-3-((2S,3R)-5-benzyloxy-3-hydroxy-2-methylpentanoyl)-2-oxazolidinone 
• 1416567-75-3 C₂₉H₄₁NO₅Si 
• 135799-62-1 Benzoic acid (3R,4R)-3-(tert-butyl-dimethyl-silanyloxy)-4-methyl-5-(tetrahydro-pyran-2-yloxy)-pentyl ester 
• 135799-61-0 Benzoic acid (3R,4R)-3-hydroxy-4-methyl-5-(tetrahydro-pyran-2-yloxy)-pentyl ester 
• 135799-57-4 (E)-(S)-4-Methyl-5-(tetrahydro-pyran-2-yloxy)-pent-2-enoic acid methyl ester 
• 135799-63-2 (3R,4R)-3-(tert-Butyl-dimethyl-silanyloxy)-4-methyl-5-(tetrahydro-pyran-2-yloxy)-pentan-1-ol 
• 135799-58-5 (E)-(S)-4-Methyl-5-(tetrahydro-pyran-2-yloxy)-pent-2-en-1-ol 
• 135799-59-6 {(2R,3S)-3-[(R)-1-Methyl-2-(tetrahydro-pyran-2-yloxy)-ethyl]-oxiranyl}-methanol 
• 135799-60-9 (3R,4R)-4-Methyl-5-(tetrahydro-pyran-2-yloxy)-pentane-1,3-diol 
• 69739-34-0 t-butyldimethylsiyl triflate 
• 135799-64-3 [(1R,2R)-1-(2-Benzyloxy-ethyl)-2-methyl-3-(tetrahydro-pyran-2-yloxy)-propoxy]-tert-butyl-dimethyl-silane 

Downstream Products

• 135799-66-5 (2S,3R)-5-(benzyloxy)-3-((tert-butyldimethylsilyl)oxy)-2-methylpentanal 
• 1202022-06-7 (28R,29R)-arenamide A 
• 1412911-49-9 C₃₆H₅₇N₅O₇ 
• 1412893-35-6 C₃₆H₅₉N₅O₈ 
• 1412893-36-7 C₃₆H₅₉N₅O₈ 
• 1412893-38-9 C₄₈H₇₃N₅O₉ 
• 1412893-39-0 C₄₈H₇₃N₅O₉ 
• 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 
• 135799-73-4 (2S,3R)-2-<(1R,2R)-4-(Benzyloxy)-2-<(tert-butyldimethylsilyl)oxy>-1-methylbutyl>-3-<(2R)-3-hydroxy-2-methylpropyl>-5-methoxy-1,2,3,4-tetrahydrofuran 

Relevant academic research and scientific papers

Total syntheses of 28,29-diepi-arenamide A, 29-epi-arenamide A, and 28-epi-arenamide A

This communication describes the synthesis of stereochemical analogs of arenamide A, a 19-membered cytotoxic depsipeptide isolated from the fermentation broth of a marine bacterial strain Salinispora arenicola. The key steps are diastereoselective aldol r

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