173656-67-2

Upstream product

• 173536-90-8 (Z)-3-methyl-1-tetrahydropyranyloxy-3-hexen-6-ol 
• 173536-83-9 Methanesulfonic acid (3E,5E)-7-(tert-butyl-diphenyl-silanyloxy)-hepta-3,5-dienyl ester 
• 173536-82-8 tert-Butyl-diphenyl-[(2E,4E)-7-(tetrahydro-pyran-2-yloxy)-hepta-2,4-dienyloxy]-silane 
• 172473-07-3 (E-E)-1-tert-butyldiphenylsiloxy-2,4-heptadien-7-ol 
• 149650-06-6 (E,E)-ethyl 7-tetrahydropyranyloxy-2,4-heptadienoate 
• 115524-30-6 (E)-5-(Tetrahydro-pyran-2-yloxy)-pent-2-enal 
• 92844-99-0 (2E)-5-<(2-tetrahydropyranyl)oxy>pent-2-en-1-ol 
• 149310-67-8 ethyl (E)-5-((tetrahydro-2H-pyran-2-yl)oxy)pent-2-enoate 
• 149311-09-1 (2E,4E)-7-(Tetrahydro-pyran-2-yloxy)-hepta-2,4-dien-1-ol 
• 173656-68-3 (3Z,10E,12E)-3-methyl-14-tert-butyldiphenylsiloxy-7,7-bis(methoxycarbonyl)-1-tetrahydropyranyloxy-tetradeca-3,10,12-triene 
• 173536-84-0 (E,E)-8-tert-butyldiphenylsiloxy-1,1-bis(methoxycarbonyl)-4,6-octadiene 
• 144344-22-9 Methanesulfonic acid (Z)-4-methyl-6-(tetrahydro-pyran-2-yloxy)-hex-3-enyl ester 
• 124-63-0 methanesulfonyl chloride 
• 173656-64-9 (3Z,10E,12E)-3-methyl-14-tert-butyldiphenylsiloxy-7,7-bis(methoxycarbonyl)-tetradeca-3,10,12-trienol 

Downstream Products

• 173656-65-0 (5Z,12E,14E)-16-(tert-Butyl-diphenyl-silanyloxy)-2,9,9-tris-methoxycarbonyl-5-methyl-hexadeca-5,12,14-trienoic acid methyl ester 

Relevant academic research and scientific papers

Studies on the transannular Diels-Alder reaction of 15-membered macrocyclic trienes containing a trans-trans diene. Part I: Synthesis and isomerization of various model cyclopentadecatrienes

The transannular Diels-Alder reaction of 15-membered macrocyclic trienes with a trans-trans-cis (TTC) olefin geometry can lead to A.B.C. tricyclic products of trans-syn-trans (TST) and cis-syn-cis (CSC) stereochemistry whereas the TTT isomers can p

Transannular Diels-Alder Reaction of Trans-Trans-Cis 15-Membered Macrocyclic Trienes. Evidence for Asynchronous Transition State.

The transannular Diels-Alder reaction of trans-trans-cis 15-membered macrocyclic trienes 1, 6, 7 leading to A.B.C. tricyclic compounds is described.