733010-82-7

Upstream product

• 733010-77-0 (7E,11E)-(3R,4S)-13-Benzyloxy-4-(1-ethoxy-ethoxy)-3-hydroxy-3,7,11-trimethyl-trideca-7,11-dienenitrile 
• 733010-78-1 (7E,11E)-(3R,4S)-13-Benzyloxy-3,4-dihydroxy-3,7,11-trimethyl-trideca-7,11-dienenitrile 
• 733010-80-5 [(4R,5S)-5-((3E,7E)-9-Benzyloxy-3,7-dimethyl-nona-3,7-dienyl)-2,2,4-trimethyl-[1,3]dioxolan-4-yl]-acetonitrile 
• 733010-76-9 (R)-2-[(4E,8E)-(S)-10-Benzyloxy-1-(1-ethoxy-ethoxy)-4,8-dimethyl-deca-4,8-dienyl]-2-methyl-oxirane 
• 733010-74-7 (6E,10E)-(S)-12-Benzyloxy-2,6,10-trimethyl-dodeca-1,6,10-trien-3-ol 
• 733010-75-8 (4E,8E)-(S)-10-Benzyloxy-4,8-dimethyl-1-((R)-2-methyl-oxiranyl)-deca-4,8-dien-1-ol 
• 71135-48-3 (2E,6E,10E)-1-Benzyloxy-3,7,11-trimethyldodeca-2,6,10-trien-12-ol 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 733010-81-6 2-[(4R,5S)-5-((3E,7E)-9-Benzyloxy-3,7-dimethyl-nona-3,7-dienyl)-2,2,4-trimethyl-[1,3]dioxolan-4-yl]-ethanol 

Relevant academic research and scientific papers

Toward the total synthesis of methyl isosartortuoate: Construction of the backbone of the diene unit

The backbone of diene precursor in the proposed biogenesis of methyl isosartortuoate through a Diels-Alder reaction has been constructed via dehydration to establish the conjugated system; and double cyclization by using Horner-Wittig-Emmons reaction and