21634-43-5

Upstream product

• 15466-96-3 3-isobutoxy-5,5-dimethylcyclohex-2-en-1-one 
• 593-60-2 Vinyl bromide 
• 6267-39-6 3-ethoxy-5,5-dimethyl-2-cyclohexen-1-one 
• 1017276-29-7 C₁₀H₁₆O 
• 92249-36-0 5,5-dimethyl-3-oxocyclohex-1-en-1-yl 4-nitrobenzenesulfonate 
• 7486-35-3 tri-n-butyl(vinyl)tin 
• 126-81-8 dimedone 

Downstream Products

• 56621-35-3 3-formyl-5,5-dimethyl-2-cycolohexen-1-one 
• 84132-65-0 rac-5,5-dimethyl-3-vinylcyclohex-2-en-1-ol 
• 106144-74-5 5,5-Dimethyl-3-prop-2-ynyloxy-1-vinyl-cyclohexene 
• 370558-07-9 1-Acetoxy-3,3-dimethyl-5-vinylcyclohexa-1,5-diene 
• 84132-66-1 5,5-dimethyl-1-(2-propenoxy)-3-vinylcyclohex-2-ene 

Relevant academic research and scientific papers

Vinyl nosylates: An ideal partner for palladium-catalyzed cross-coupling reactions

In a hurry to leave! Nosylates act as an excellent leaving group in various palladium-catalyzed cross-couplings, such as Suzuki, Stille, Heck, and Sonogashira reactions (see scheme). Crystalline, stable, and cheap vinyl and aryl nosylates proved better th

Conformational biasing in 1,3-oxidative rearrangements of dienols

1-Vinyl-2-cycloalkenols are oxidized to form conjugated dienones in useful yields. Although this oxidative rearrangement is general, severe steric interactions can favor the formation of a conjugated dienal instead of a conjugated dienone. Several heteroc

Syntheses of angucyclinones related to ochromycinone

Two synthetic approaches have been investigated for the syntheses of model angucyclinones related to ochromycinone. The first involves a Diels-Alder/Friedel-Crafts strategy in which the Diels-Alder adduct formed between dimethyl acetylenedicarboxylate and