650605-38-2

Upstream product

• 91-48-5 (E)-2,3-diphenylpropenoic acid 
• 141-78-6 ethyl acetate 
• 58085-33-9 α-phenylcinnamoyl chloride 

Downstream Products

• 650605-52-0 5-(2-methoxy-ethoxymethoxymethyl)-2,3,4-triphenyl-cyclopent-2-enol 
• 650605-48-4 2-benzylidene-3-oxo-4,5-diphenyl-pent-4-enoic acid diethylamide 
• 650605-53-1 5-hydroxymethyl-2,3,4-triphenyl-cyclopent-3-en-2-ol 
• 650605-43-9 2-ethylidene-3-oxo-4,5-diphenyl-pent-4-enoic acid ethyl ester 
• 650605-42-8 2-benzylidene-3-oxo-4,5-diphenyl-pent-4-enoic acid ethyl ester 
• 38661-88-0 (E)-1,2-diphenylbut-1-en-3-one 

Relevant academic research and scientific papers

Cationic vanadium(IV) complexes as efficient catalysts for nazarov cyclizations

Vanadium(IV) species generated in situ from V(salen)Cl2 complexes (1) by reaction with 2 equiv. of AgSbF6 are effective catalysts for Nazarov cyclizations. Thus, dialkenyl ketones bearing α-ester groups are efficiently converted to c

Catalytic Asymmetric Nazarov Reactions Promoted by Chiral Lewis Acid Complexes

(Equation presented) Divinyl ketones bearing α-ester or α-amide groups undergo Nazarov cyclizations to give cylopentenones using copper-bisoxazoline Lewis acid complexes with moderate to good ees.