Cyclization of o -Alkynylisocyanobenzenes with 1,3-Dicarbonyl Compounds.

Autor: La-ongthong, Kannika, Sawekteeratana, Natthapat, Klaysuk, Jasarin, Soorukram, Darunee, Leowanawat, Pawaret, Reutrakul, Vichai, Krobthong, Sucheewin, Wongtrakoongate, Patompon, Kuhakarn, Chutima
Předmět:
Zdroj: Synlett; Sep2022, Vol. 33 Issue 14, p1411-1418, 8p
Abstrakt: A facile and convenient reaction of o -alkynylisocyanobenzenes with various active-methylene compounds, including 1,3-diesters, 1,3-diketones, β-keto esters, and β-keto amides, under Brønsted basic conditions, has been developed. Diethyl malonate reacted smoothly with a collection of o -alkynylisocyanobenzenes to provide the corresponding 2-quinolin-2-yl malonates in excellent yields. Acetylacetone gave a mixture of quinolin-4-yl and quinolin-2-yl derivatives. Acetoacetate esters and acetoacetyl amide derivative initially gave 2-quinolin-2-yl adducts that underwent partial deacetylation under the reaction conditions. [ABSTRACT FROM AUTHOR]
Databáze: Complementary Index