Yao, Tuanli published the artcileSynthesis of Isocoumarins and α-Pyrones via Electrophilic Cyclization, Safety of Dimethyl 2-iodoterephthalate, the publication is Journal of Organic Chemistry (2003), 68(15), 5936-5942, database is CAplus and MEDLINE.
A variety of substituted isocoumarins, e.g. I [R1 = H, MeO; R2 = H, MeO, MeO2C; R3 = HO(CH2)3, Ph, n-hexyl, etc.; R4 = H, iodo, 4-O2NC6H4S, PhSe], and α-pyrones, e.g. II [R5 = H, Me, Ph; R6 = H, Ph; R5R6 = (CH2)3; R7 = Bu, Ph], are readily prepared in excellent yields under very mild reaction conditions by the reaction of o-(1-alkynyl)benzoates, e.g. III (R8 = Me, Me3C), or (Z)-2-alken-4-ynoates, e.g. IV (R9 = Me, Et), resp., with ICl, I2, PhSeCl, p-O2NC6H4SCl, and hydrogen iodide. This methodol. accommodates various alkynyl esters and has been successfully extended to the synthesis of polycyclic aromatic and biaryl compounds
Journal of Organic Chemistry published new progress about 165534-79-2. 165534-79-2 belongs to iodides-buliding-blocks, auxiliary class Iodide,Benzene,Ester, name is Dimethyl 2-iodoterephthalate, and the molecular formula is C27H39ClN2, Safety of Dimethyl 2-iodoterephthalate.
Referemce:
https://en.wikipedia.org/wiki/Iodide,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com