1568951-23-4

Upstream product

• 1351977-01-9 (2R,3S)-2-amino-3-methoxyhex-5-en-1-ol 
• 171822-71-2 (1R,2S)-N-tert-butoxycarbonyl-[1-(tert-butyldimethylsilyloxymethyl)-2-hydroxypent-4-enyl]amine 
• 171564-54-8 [(R)-1-(tert-butyldimethylsilanyloxymethyl)-2-oxopent-4-enyl]carbamic acid tert-butyl ester 
• 126-30-7 2,2-Dimethyl-1,3-propanediol 
• 824-94-2 p-methoxybenzyl chloride 
• 1414941-34-6 C₂₈H₄₉NO₆Si 
• 1414941-23-3 (S)-3-(tert-butyldimethylsilyloxy)-5-(4-methoxybenzyloxy)-4,4-dimethylpentanoic acid 
• 1414941-33-5 methyl 2-(2-(4-methoxybenzyloxy)ethyl)oxazole-4-carboxylate 
• 1414941-22-2 (S)-tert-butyl(1-(4-methoxybenzyloxy)-2,2-dimethylhex-5-en-3-yloxy)dimethylsilane 
• 869062-10-2 1-(4-methoxy-benzyloxy)-2,2-dimethyl-hex-5-en-3-ol 
• 446264-36-4 3-[(4-methoxyphenyl)methoxy]-2,2-dimethyl-propan-1-ol 

Downstream Products

• 1414941-24-4 C₂₈H₄₅NO₅Si 
• 1416812-87-7 C₃₃H₅₅NO₇Si 
• 1392284-86-4 (2S,5S,7S)-7-[(tert-butyldimethylsilyl)oxy]-5-hydroxy-1-[(4-methoxybenzyl)oxy]-8-{4-[(S)-1-methoxybut-3-en-1-yl]oxazol-2-yl}-2,6,6-trimethyloctan-3-one 
• 1392284-87-5 (2S,5R,7S)-7-[(tert-butyldimethylsilyl)oxy]-5-hydroxy-1-[(4-methoxybenzyl)oxy]-8-{4-[(S)-1-methoxybut-3-en-1-yl]oxazol-2-yl}-2,6,6-trimethyloctan-3-one 
• 1392284-88-6 C₃₃H₅₅NO₇Si 
• 1392284-89-7 (2S,4S,6S,7S)-2-[(tert-butyldimethylsilyl)oxy]-6-methoxy-8-[(4-methoxybenzyl)oxy]-1-{4-[(S)-1-methoxybut-3-en-1-yl]oxazol-2-yl}-3,3,7-trimethyloctan-4-ol 
• 1392284-90-0 C₃₃H₅₅NO₇Si 
• 1392284-91-1 C₃₄H₅₇NO₇Si 
• 1392284-92-2 (2S,6S,7S)-2-[(tert-Butyldimethylsilyl)oxy]-6-methoxy-8-[(4-methoxybenzyl)oxy]-1-{4-[(S)-1-methoxybut-3-en-1-yl]oxazol-2-yl}-3,3,7-trimethyloctan-4-one 
• 1414941-27-7 C₄₀H₆₈BNO₉Si 
• 1414941-28-8 C₄₀H₆₈BNO₉Si 
• 1414941-25-5 C₄₈H₈₂INO₁₀Si₂ 

Relevant academic research and scientific papers

Modular total synthesis of rhizopodin: A highly potent G-actin dimerizing macrolide

A highly convergent total synthesis of the potent polyketide macrolide rhizopodin has been achieved in 29steps by employing a concise strategy that exploits the molecule′s C2 symmetry. Notable features of this convergent approach include a rapid assembly of the macrocycle through a site-directed sequential cross-coupling strategy and the bidirectional attachment of the side chains by means of Horner-Wadsworth-Emmons (HWE) coupling reactions. During the course of this endeavor, scalable routes for synthesis of three main building blocks of similar complexity were developed that allowed for their stereocontrolled construction. This modular route will be amenable to the development of syntheses of other analogues of rhizopodin.