TY  - JOUR
AB  - The examination of the palladium catalysed arylation reactions of mono-iodo derivatives of the phenyl and benzyl esters of benzoic acid, phenylacetic acid and dehydrocinnamic acid has resulted in the formation of benzo[c]chromen-6-ones, unexpected cinnamate and succinate products and diphenyl dimers. Many of these products can be rationalised as arising from novel cyclic ArPd(II)-enolate intermediates, formed by intramolecular C-H activation by ArPd(II). Crown Copyright © 2007.
AU  - Taylor, SR
AU  - Ung, AT
AU  - Pyne, SG
DA  - 2007/10/05
DO  - 10.1016/j.tet.2007.08.080
EP  - 10895
JO  - Tetrahedron
PY  - 2007/10/05
SP  - 10889
TI  - Synthesis of benzo[c]chromen-6-ones via novel cyclic aryl-Pd(II)-ester enolate intermediates
VL  - 63
Y1  - 2007/10/05
Y2  - 2026/05/29
ER  -