68705-88-4

Upstream product

• 104-53-0 3-phenyl-propionaldehyde 
• 36934-19-7 2,3,3-trimethyl-4-penten-2-ol 
• 27644-02-6 2,2-dimethyl-1-phenylbut-3-en-1-ol 
• 71787-60-5 4,4-dimethyl-1-phenyl-hex-5-en-3-ol 
• 870-63-3 prenyl bromide 

Downstream Products

• 944546-84-3 5-bromo-6-methyl-1-phenylhept-5-ene-3-thiol 
• 944546-82-1 S-5-bromo-6-methyl-1-phenylhept-5-en-3-yl ethanethioate 
• 944546-81-0 5-bromo-6-methyl-1-phenylhept-5-en-3-ol 

Relevant academic research and scientific papers

Surprisingly efficient catalytic Cr-mediated coupling reactions

(Chemical Equation Presented) With use of 1 mol % of Cr catalyst 5, surprisingly efficient Cr-mediated couplings of aldehydes with various types of nucleophiles have been realized. The catalyst set of Cr catalyst 5 and Ni catalyst 4 is used for alkenylati

New and stereoselective synthesis of 1,4-disubstituted buten-4-ols (homoallylic alcohol α-adducts) from the corresponding γ-isomers (3,4-disubstituted buten-4-ols) via an acid-catalyzed allyl-transfer reaction with aldehydes

The γ-adducts of homoallylic alcohols 3, derived from aldehydes via the usual reaction with common allylic metals 1, were converted to the corresponding α-adducts 6 by an acid-catalyzed allyl-transfer reaction. In the allyl-transfer reaction, anti-and syn