1434591-03-3Relevant academic research and scientific papers
Hypervalent iodine(III)-mediated benzannulation of enamines with alkynes: An efficient synthesis of substituted aminonaphthoic acid derivatives
Gao, Peng,Fan, Mingjin,Bai, Zijing,Wei, Yunyang
supporting information, p. 479 - 485 (2015/04/22)
An intermolecular two C-C bond formation procedure for the synthesis of carbocycles mediated by hypervalent iodine(III) reagents was developed. This metal free protocol provided a new approach for the synthesis of useful substituted 1-amino-2-naphthoic ac
Hypervalent iodine(III)-mediated benzannulation of enamines with alkynes for the synthesis of polysubstituted naphthalene derivatives
Gao, Peng,Liu, Jinjian,Wei, Yunyang
supporting information, p. 2872 - 2875 (2013/07/19)
A series of functionalized 1-amino-2-naphthalenecarboxylic acid derivatives were synthesized from enamines and alkynes via a benzannulation strategy mediated by iodosylbenzene and BF3·Et2O. The advantages of this novel benzannulation process include broad substrate scope, good functional group tolerance, and mild reaction conditions without the use of heavy metals.
