39159-74-5Relevant academic research and scientific papers
Fe-Catalyzed tandem cyclization for the synthesis of 3-nitrofurans from homopropargylic alcohols and Al(NO3)3·9H2O
Wang, Ting,Jiang, Yong,Wang, Yanyan,Yan, Rulong
supporting information, p. 5232 - 5235 (2018/08/03)
Al(NO3)3·9H2O as a nitro source for the synthesis of 3-nitrofurans from homopropargylic alcohols through Fe-catalyzed tandem cyclization is described. In this transformation, the substituted nitrofurans are obtained throug
A method for accessing sulfanylfurans from homopropargylic alcohols and sulfonyl hydrazides
Yan, Rulong,Yang, Xiaodong
supporting information, p. 3571 - 3574 (2019/06/13)
A sulfenylation/cyclization reaction has been developed for the synthesis of sulfanylfurans in the presence of iodine. These processes provide facile strategies to construct C-S/O bonds, and expand the methods of synthesizing sulfanylfurans. In this trans
Regioselective access to CF3S-substituted dihydrofurans from homopropargylic alcohols with trifluoromethanesulfenamide
Chen, Dao-Qian,Gao, Pin,Zhou, Ping-Xin,Song, Xian-Rong,Qiu, Yi-Feng,Liu, Xue-Yuan,Liang, Yong-Min
supporting information, p. 6637 - 6639 (2015/04/14)
A facile access to 4-((trifluoromethyl)thio)-2,3-dihydrofurans from unprotected homopropargylic alcohols in high regioselectivity is reported. This method is the first example of using a free hydroxy group as a nucleophile to complete a trifluoromethylthiolation/cyclization protocol with an alkyne in moderate to excellent yields. This journal is
