1096706-74-9

Upstream product

• 79027-28-4 (2S)-3-(benzyloxy)-2-methylpropanal 
• 1096707-44-6 methyl (2S,3S,4S)-3,5-bis(benzyloxy)-2,4-dimethylpentanoate 
• 1096707-45-7 (2R,3R,4S)-3,5-bis(benzyloxy)-2,4-dimethylpentan-1-ol 

Downstream Products

• 1096706-98-7 methyl (2S,3R,4R,5S,6S)-5,7-bis(benzyloxy)-2-bromo-3-hydroxy-2,4,6-trimethylheptanoate 
• 1333041-55-6 (-)-(2R,3R,4R,5S,6S)-3,5,7-tris(benzyloxy)-2,4,6-trimethylheptan-1-ol 
• 1333040-68-8 (+)-(2S,3S,4S,5S,6S)-3,5,7-tris(benzyloxy)-2,4,6-trimethylheptanal 
• 1333041-61-4 (+)-(4S,5S,6S,7S,8S,9S,10S)-ethyl 7,9,11-tris(benzyloxy)-4,6,8,10-tetramethyl-5-(triethylsilyloxy)undecanoate 
• 1333041-63-6 (+)-methyl 2-bromo-2-((2S,5S,6S)-5-methyl-6-((2S,3S,4S,5S,6S)-3,5,7-tris(benzyloxy)-4,6-dimethylheptan-2-yl)tetrahydro-2H-pyran-2-yl)propanoate 
• 1333041-65-8 (+)-(2S,3S,4S,5S,6S,7S,8S)-5,7,9-tris(benzyloxy)-2,4,6,8-tetramethyl-3-(triethylsilyloxy)nonan-1-ol 
• 1333040-74-6 (+)-(2R,3R,4S,5S,6S,7S,8S)-5,7,9-tris(benzyloxy)-2,4,6,8-tetramethyl-3-(triethylsilyloxy)nonanal 
• 1333041-59-0 (+)-(4S,5S,6S,7S,8S,9S,10S,E)-ethyl 7,9,11-tris(benzyloxy)-4,6,8,10-tetramethyl-5-(triethylsilyloxy)undec-2-enoate 
• 1333041-67-0 (+)-(4S,5S,6S,7S,8S,9S,10S)-7,9,11-tris(benzyloxy)-4,6,8,10-tetramethyl-5-(triethylsilyloxy)undecan-1-ol 
• 1333040-78-0 (+)-(4S,5S,6S,7S,8S,9S,10S)-7,9,11-tris(benzyloxy)-4,6,8,10-tetramethyl-5-(triethylsilyloxy)undecanal 
• 1333041-47-6 (-)-(3R,4R,5R,6S,7S,8S)-methyl 5,7,9-tris(benzyloxy)-2-bromo-3-hydroxy-2,4,6,8-tetramethylnonanoate 
• 1333040-71-3 (-)-(2R,3R,4R,5R,6S,7S,8S)-methyl 5,7,9-tris(benzyloxy)-3-hydroxy-2,4,6,8-tetramethylnonanoate 
• 1333041-51-2 (+)-(2S,3S,4S,5S,6S)-methyl 3,5,7-tris(benzyloxy)-2,4,6-trimethylheptanoate 
• 1333041-53-4 (+)-(2R,3R,4S,5S,6S,7S,8S)-methyl 5,7,9-tris(benzyloxy)-2,4,6,8-tetramethyl-3-(triethylsilyloxy)nonanoate 

Relevant academic research and scientific papers

A bidirectional approach to the synthesis of polypropionates: Synthesis of C1-C13 fragment of zincophorin and related isomers

The structure-activity study of a bioactive natural product containing polypropionate subunits requires that its stereoisomers also be evaluated. Therefore, a general approach to synthesize these motifs is necessary. We describe herein the synthesis of the C1 - C13 polypropionate subunit of zincophorin and isomers there of using a two-reaction sequence: an aldol reaction using a mixture of tetrasubstituted enoxysilanes and a hydrogen-transfer reaction, both under Lewis acid control. Selection of the appropriate Lewis acid dictates the stereochemical outcome of these reactions. From a tactical standpoint, this study shows how a polypropionate sequence can be read and constructed in two directions, either the east-west or the west-east approaches. The choice of the optimal route is influenced by the number of complexation sites that can interfere in the aldol step under bidentate Lewis acid control.

Stereopentads derived from a sequence of Mukaiyama aldolization and free radical reduction on α-methyl-β-alkoxy aldehydes: A general strategy for efficient polypropionate synthesis

(Chemical Equation Presented) In a stereodivergent manner, all 16 diastereomeric stereopentads 7-22 were synthesized starting with α-methyl-β-alkoxy aldehydes 25 and 27. We designed an approach based on a sequence of a Mukaiyama aldolization with enoxysil