377750-91-9

Upstream product

• 88406-01-3 2,3-O-isopropylidene-1-C-<(1R)-1-methylprop-2-enyl>-D-erythro-glycerol 
• 377750-99-7 (2E,5R,6S,7R)-7,8-(isopropylidene)dioxy-6-[(4-methoxyphenyl)methoxy]-5-methyl-1-pivaloyloxy-2-octene 
• 377751-00-3 (2R,3S,4R,6E)-3-[(4-methoxyphenyl)methoxy]-4-methyl-8-pivaloyloxy-6-octene-1,2-diol 
• 377751-01-4 (3S,4R,6E)-1,1-dibromo-3-[(4-methoxyphenyl)methoxy]-4-methyl-8-pivaloyloxy-1,6-octadiene 
• 377750-97-5 (2E,5R,6S,7R)-7,8-(isopropylidene)dioxy-6-[(4-methoxyphenyl)methoxy]-5-methyl-2-octenoate 
• 377750-98-6 (2E,5R,6S,7R)-7,8-(isopropylidene)dioxy-6-[(4-methoxyphenyl)methoxy]-5-methyl-2-octen-1-ol 
• 377751-02-5 (2E,5R,6S)-8,8-dibromo-6-[(4-methoxyphenyl)methoxy]-5-methyl-2,7-octadien-1-ol 
• 377750-96-4 (3R,4S,5R)-5,6-(isopropylidene)dioxy-4-[(4-methoxyphenyl)methoxy]-3-methyl-1-hexanol 
• 377750-95-3 (3R,4S,5R)-5,6-(isopropylidene)dioxy-4-[(4-methoxyphenyl)methoxy]-3-methyl-1-hexene 
• 917079-87-9 (3R,4S)-4-((R)-2,2-Dimethyl-[1,3]dioxolan-4-yl)-4-(4-methoxy-benzyloxy)-3-methyl-butyraldehyde 
• 824-94-2 p-methoxybenzyl chloride 
• 76-83-5 trityl chloride 
• 377751-11-6 (2E,5R,6S,9E)-1-(tert-butyldiphenylsilyloxy)-6-[(4-methoxyphenyl)methoxy]-5-methyl-12-(triphenylmethoxy)-2,9-dodecadien-7-yne 
• 377751-12-7 (2E,5R,6S,7Z,9E)-1-(tert-butyldiphenylsilyloxy)-6-[(4-methoxyphenyl)methoxy]-5-methyl-12-(triphenylmethoxy)-2,7,9-dodecatriene 

Downstream Products

• 377750-90-8 (1S,2S,3S,4Z,6S,7S,8R)-2-formyl-7-[(4-methoxyphenyl)methoxy]-8-methyl-3-[2-(triphenylmethoxy)ethyl]bicyclo[4.3.0]non-4-ene 

Relevant academic research and scientific papers

Total synthesis of macquarimicins using an intramolecular Diels-Alder approach inspired by a biosynthetic pathway

A total synthesis of the macquarimicins A-C (1-3), novel natural products with intriguing tetra- or pentacyclic frameworks, has been achieved. The synthesis features an extensive investigation of the biosynthesis-based intramolecular Diels-Alder (IMDA) re

Synthetic study of macquarimicins: Highly stereoselective construction of the AB-ring system

matrix presented The highly stereoselective synthesis of the AB-ring system of macquarimicins, a novel class of microbial metabolites with inhibitory activity for neutral sphingomyelinase, has been achieved. The present synthesis features the highly stere