128440-08-4

Upstream product

• 128308-32-7 (3R,4R)-4-Benzyloxy-3-hydroxy-pentanenitrile 
• 75-66-1 2-methylpropan-2-thiol 
• 81927-55-1 O-benzyl 2,2,2-trichloroacetimidate 
• 1323952-38-0 C₁₄H₂₀O₃ 

Downstream Products

• 1323952-31-3 C₁₈H₂₆O₅ 
• 1323952-42-6 C₂₂H₃₈O₃SSi 
• 1323952-43-7 C₂₄H₄₀O₅Si 
• 1323952-32-4 C₁₈H₂₈O₅ 
• 1323952-33-5 C₁₄H₁₈O₄ 
• 1323952-44-8 C₂₀H₃₂O₄Si 
• 1323952-45-9 C₂₇H₄₆O₆Si 
• 128308-14-5 (1R,3R,4S,5S,9R,13S,14R)-9-((R)-1-Benzyloxy-ethyl)-3-[(1S,4S)-4-(3-benzyloxy-phenyl)-4-methoxy-1-methyl-butyl]-4,14,16,16-tetramethyl-2,6,10,17-tetraoxa-tricyclo[11.3.1.1^1,5]octadecane-7,11-dione 
• 125791-99-3 3-deoxydebromoaplysiatoxin 
• 128308-13-4 {(2S,3R,6R,8R,9S,10S)-8-[(1S,4S)-4-(3-Benzyloxy-phenyl)-4-methoxy-1-methyl-butyl]-10-hydroxy-3,5,5,9-tetramethyl-1,7-dioxa-spiro[5.5]undec-2-yl}-acetic acid (1R,2R)-2-benzyloxy-1-tert-butylsulfanylcarbonylmethyl-propyl ester 

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

SYNTHETIC STUDY ON APLYSIATOXINS, HIGHLY INFLAMMATORY AGENTS AND TUMOR PROMOTERS. SYNTHESIS OF THE THREE OPTICALLY ACTIVE SEGMENTS

The main segments in debromoaplysiatoxin and related aplysiatoxins have been efficiently synthesized from D-glucose and L- and D-tartaric acids.