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Volumn 58, Issue 44, 2002, Pages 9063-9074

Titanium(IV) bromide and boron(III) tribromide promoted reactions of arylaldehydes with 3-butyn-2-one, methyl propiolate and propynenitrile

Author keywords

3 butyn 2 one; Methyl propiolate; Propynenitrile; Titanium(IV) bromide

Indexed keywords

ALDEHYDE DERIVATIVE; BORON TRIBROMIDE; BROMINE DERIVATIVE; CHEMICAL COMPOUND; KETONE DERIVATIVE; LEWIS ACID; METHYLPROPIOLATE; NITRILE; PALLADIUM; TITANIUM BROMIDE; UNCLASSIFIED DRUG;

EID: 0037191026     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(02)01127-4     Document Type: Article
Times cited : (10)

References (29)
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    • In a short communication, we reported that when the reaction of arylaldehydes with 3-butyn-2-one was carried out at <-20°C, the brominated compounds 1 were obtained as the major product, however, when the reaction was carried out at room temperature (20°C), both 1 and α,β-dibrominated compounds 2 were formed as the major products. See: Shi M., Wang C.-J. Helv. Chim. Acta. 85:2002;841.
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    • . The Suzuki-type coupling reaction of boronic acids with benzyl bromide has been reported before: (a) Chowdhury S., Georgghiou P.E. Tetrahedron Lett. 40:1999;7599 (b) Chen H., Deng M.-Z. J. Chem. Soc., Perkin Trans. 1. 2000;1609.
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