791810-20-3

Upstream product

• 321852-62-4 (3E,7Z)-11-Iodo-3,6,6-trimethyl-undeca-3,7-dien-10-ynal 
• 791810-18-9 (3E,7Z)-11-Iodo-3,6,6-trimethyl-undeca-3,7-dien-10-ynal 
• 35066-34-3 methyl (E)-3-methyl-5-<(2-tetrahydropyranyl)oxy>pent-2-enoate 
• 104939-54-0 methyl 5-(tetrahydro-2H-pyran-2-yloxy)pent-2-ynoate 
• 90708-82-0 5-<(tert-Butyldimethylsilyl)oxy>-3-methyl-2(E)-penten-1-ol 
• 321852-64-6 (E)-5-(tert-Butyl-dimethyl-silanyloxy)-3-methyl-pent-2-enoic acid methyl ester 
• 848079-71-0 (6E)-1-iodo-9-(tetrahydro-2H-pyran-2-yloxy)-4,4,7-trimethylnone-2,6-diene 
• 848079-78-7 (4E,8E)-11-(tetrahydro-2H-pyran-2-yloxy)-6,6,9-trimethylundeca-4,8-dien-1-yne 
• 791809-93-3 ethyl (2E,6E)-9-(tetrahydro-2H-pyran-2-yloxy)-4,4,7-trimethylnona-2,6-dienoate 
• 848079-70-9 (2E,6E)-9-(tetrahydro-2H-pyran-2-yloxy)-4,4,7-trimethylnona-2,6-dien-1-ol 
• 791810-06-5 methyl (2Z)-3-phenylsulfanyl-5-(tetrahydro-2H-pyran-2-yloxy)pent-2-enoate 
• 791810-09-8 methyl (2E)-7-(tetrahydro-2H-pyran-2-yloxy)-2,2,5-trimethylhept-4-enoate 
• 791810-10-1 (4E)-7-(tetrahydro-2H-pyran-2-yloxy)-2,2,5-trimethylhept-4-en-1-ol 
• 848079-90-3 (3E,7E)-3,6,6-trimethyl-11-iodoundeca-3,7-dien-10-yn-1-ol 

Relevant academic research and scientific papers

PtCl2-catalyzed transannular cycloisomerization of 1,5-enynes: A new efficient regio- and stereocontrolled access to tricyclic derivatives

(Chemical Equation Presented) Transannular PtCl2-catalyzed cycloisomerizations open a new route to cyclopropanic tricyclic systems. Ketones A or C were efficiently prepared from the same cycloundec-5-en-1-yne precursor B, depending on the subst

Exploration of radical transannulations inside a cycloundecadienyne

An eleven-membered macrocyclic bromomethyldimethylsilyl propargylic ether has been prepared in order to examine the regioselectivity of a transannular radical process. The vinyl radical intermediate appeared to follow exclusively a 6-(π-endo)endo-trig/7-(π-exo)exo-trig transcyclization course to create a 6,7-bicyclic skeleton.