588728-53-4

Upstream product

• 85116-38-7 (+)-diisopinocampheylallylborane 
• 206255-41-6 (3R,4R)-4-Benzyloxy-3-(4-methoxy-benzyloxy)-pentanal 
• 89104-01-8 (2R,3R)-2-(benzyloxy)-5-hexen-3-ol 
• 53346-05-7 (R)-2-benzyloxypropanal 
• 81927-55-1 O-benzyl 2,2,2-trichloroacetimidate 
• 1323952-38-0 C₁₄H₂₀O₃ 
• 206255-61-0 C₂₁H₂₆O₃ 
• 1730-25-2 allylmagnesium bromide 

Downstream Products

• 588728-60-3 {1-[3-benzyloxy-2-(4-methoxy-benzyloxy)-butyl]-but-3-enyloxy}-tert-butyl-dimethyl-silane 
• 1323952-39-1 C₂₉H₄₄O₄Si 
• 1323952-28-8 C₂₈H₄₂O₅Si 
• 1323952-29-9 C₃₅H₅₄O₆Si 
• 1323952-40-4 C₄₀H₅₈O₈SSi 
• 588728-62-5 Benzoic acid (2S,4S,6R)-6-[(2R,3R)-3-benzyloxy-2-(4-methoxy-benzyloxy)-butyl]-2-methoxy-2-[(E)-4-(4-methoxy-benzyloxy)-1,1-dimethyl-but-2-enyl]-3-oxo-tetrahydro-pyran-4-yl ester 
• 588728-61-4 (E)-(9R,11R,12R)-12-Benzyloxy-9-(tert-butyl-dimethyl-silanyloxy)-1,11-bis-(4-methoxy-benzyloxy)-4,4-dimethyl-tridec-2-ene-5,7-dione 
• 639786-30-4 (3aS,4S,6R,7aS)-6-[(2R,3R)-3-Benzyloxy-2-(4-methoxy-benzyloxy)-butyl]-4-methoxy-4-[(E)-4-(4-methoxy-benzyloxy)-1,1-dimethyl-but-2-enyl]-tetrahydro-[1,3]dioxolo[4,5-c]pyran-2-one 
• 588728-55-6 (2S,3S,4S,6S)-6-[(2R,3R)-3-Benzyloxy-2-(4-methoxy-benzyloxy)-butyl]-2-methoxy-2-[(E)-4-(4-methoxy-benzyloxy)-1,1-dimethyl-but-2-enyl]-tetrahydro-pyran-3,4-diol 
• 588728-56-7 (2S,6S)-6-[(2R,3R)-3-Benzyloxy-2-(4-methoxy-benzyloxy)-butyl]-2-methoxy-2-[(E)-4-(4-methoxy-benzyloxy)-1,1-dimethyl-but-2-enyl]-dihydro-pyran-3-one 
• 627091-01-4 (R)-2-[(2R,3R)-3-Benzyloxy-2-(4-methoxy-benzyloxy)-butyl]-6-[(E)-4-(4-methoxy-benzyloxy)-1,1-dimethyl-but-2-enyl]-2,3-dihydro-pyran-4-one 
• 639786-36-0 (3aS,4S,6R,7aS)-6-((2R,3R)-3-Benzyloxy-2-hydroxy-butyl)-4-((E)-4-hydroxy-1,1-dimethyl-but-2-enyl)-4-methoxy-tetrahydro-[1,3]dioxolo[4,5-c]pyran-2-one 
• 639786-31-5 (E)-4-[(3aS,4S,6R,7aS)-6-((2R,3R)-3-Benzyloxy-2-hydroxy-butyl)-4-methoxy-2-oxo-tetrahydro-[1,3]dioxolo[4,5-c]pyran-4-yl]-4-methyl-pent-2-enal 

Relevant academic research and scientific papers

Synthetic approaches to the bottom half fragment for bryostatin 11

An approach towards the stereoselective synthesis of the bottom half fragment of bryostatin 11 is described. Key steps -include asymmetric aldol and Saksena-Evans reduction reactions -to construct multiple stereogenic centers and thioketalization-lactoniz

BRYOSTATIN ANALOGUES, SYNTHETIC METHODS AND USES

Biologically active compounds related to the bryostatin family of compounds, having simplified spacer domains and/or improved recognition domains are disclosed, including methods of preparing and utilizing the same.

A New Synthetic Approach to the C Ring of Known as Well as Novel Bryostatin Analogues

(Equation presented) A new approach to the synthesis of the C ring subunit of known and potential bryostatin analogues is described. The convergent approach, Illustrated above, requires fewer steps and offers greater flexibility In rapidly accessing diver