111787-84-9Relevant articles and documents
Synthesis of polysubstituted furans from aryl gem-dibromoethenes
Zhang, Wensheng,Xu, Wenjing
, p. 615 - 617 (2017/08/30)
[Figure not available: see fulltext.] Synthesis of 2,3,5-trisubstituted furans can be performed at 120°C in DMF using aryl gem-dibromoethenes and ethyl acetoacetate as the starting substrates under the assistance of Ag2CO3–Cs2/
Tuning radical reactivity using iodine in oxidative C(sp3)-H/C(sp)-H cross-coupling: An easy way toward the synthesis of furans and indolizines
Tang, Shan,Liu, Kun,Long, Yue,Qi, Xiaotian,Lan, Yu,Lei, Aiwen
supporting information, p. 8769 - 8772 (2015/05/20)
Molecular iodine was found to be an effective redox catalyst for the oxidative cross-coupling of carbonyl compounds with terminal alkynes. In this work, we demonstrated that iodine could tune radical reactivity through reversible C-I bond formation for co
Direct oxidative coupling of enamides and 1,3-dicarbonyl compounds: A facile and versatile approach to dihydrofurans, furans, pyrroles, and dicarbonyl enamides
Li, Pan,Zhao, Jingjing,Xia, Chungu,Li, Fuwei
, p. 5992 - 5995 (2015/01/08)
An efficient manganese(III)-mediated oxidative coupling reaction between α-aryl enamides and 1,3-dicarbonyl compounds has been developed. A series of dihydrofurans and dicarbonyl enamides were synthesized in moderate to good yields. Moreover, these dihydrofurans could be readily transformed into the corresponding furans and pyrroles via the Paal-Knorr reaction.
