Metal-free visible-light-induced oxidative cyclization reaction of 1,6-enynes and arylsulfinic acids leading to sulfonylated benzofurans

2020 ◽  
Vol 31 (1) ◽  
pp. 67-70 ◽  
Author(s):  
Leilei Wang ◽  
Min Zhang ◽  
Yulong Zhang ◽  
Qishun Liu ◽  
Xiaohui Zhao ◽  
...  
ChemInform ◽  
2014 ◽  
Vol 45 (36) ◽  
pp. no-no
Author(s):  
Tiebo Xiao ◽  
Linyong Li ◽  
Guoliang Lin ◽  
Qile Wang ◽  
Ping Zhang ◽  
...  

Synlett ◽  
2018 ◽  
Vol 29 (07) ◽  
pp. 912-917 ◽  
Author(s):  
Parviz Ranjbar ◽  
Narjes Rezaei ◽  
Ehsan Sheikhi

A metal-free oxidative C(sp3)–N coupling process has been developed for the synthesis of 2,3-dihydroquinazolin-4(1H)-ones. The reaction between primary amines, isatoic anhydride, and benzylic alcohols in the presence of HBr in DMSO at 80 °C affords 2,3-dihydroquinazolin-4(1H)-ones in excellent yields. Under these reaction conditions, benzylic alcohols react with in situ generated bromodimethylsulfonium bromide to form alkoxysulfonium intermediates. These intermediates undergo an oxidative cyclization reaction with primary amines and isatoic anhydride to produce the title products.


2015 ◽  
Vol 11 ◽  
pp. 425-430 ◽  
Author(s):  
Zhongwei Liang ◽  
Song Xu ◽  
Wenyan Tian ◽  
Ronghua Zhang

A novel and simple strategy for the efficient synthesis of the corresponding tetrahydroquinolines from N,N-dimethylanilines and maleimides using visible light in an air atmosphere in the presence of Eosin Y as a photocatalyst has been developed. The metal-free protocol involves aerobic oxidative cyclization via sp3 C–H bond functionalization process to afford good yields in a one-pot procedure under mild conditions.


RSC Advances ◽  
2014 ◽  
Vol 4 (11) ◽  
pp. 5815 ◽  
Author(s):  
Twinkle Keshari ◽  
Vishnu P. Srivastava ◽  
Lal Dhar S. Yadav

2019 ◽  
Vol 21 (16) ◽  
pp. 4406-4411 ◽  
Author(s):  
Palani Natarajan ◽  
Deachen Chuskit ◽  
Priya Priya

A metal-free, visible-light (blue LED: hν = 425 ± 15 nm) photoredox-catalyzed intramolecular cyclization reaction of N-biarylglycine esters to phenanthridine-6-carboxylates in water under an open air atmosphere at ambient conditions has been developed.


2014 ◽  
Vol 16 (5) ◽  
pp. 2418-2421 ◽  
Author(s):  
Tiebo Xiao ◽  
Linyong Li ◽  
Guoliang Lin ◽  
Qile Wang ◽  
Ping Zhang ◽  
...  

Irradiation of hydrazines and 2-isocyanobiphenyls with visible-light in the presence of organic dye eosin B generates various 6-substituted phenanthridines in good yields.


Author(s):  
Farzaneh Ansari ◽  
Hormoz Khosravi ◽  
Alireza Abbasi Kejani ◽  
Mahsa Armaghan ◽  
Walter Frank ◽  
...  

K2S2O8 is introduced as an oxygen source and C–H functionalization agent in a novel selective metal-free oxidative cyclization of enynals to synthesize α-pyrone derivatives with a relatively broad substrate scope via the formation of two C–O bonds.


2021 ◽  
Author(s):  
Arup Dutta ◽  
Mostofa Ataur Rohman ◽  
Ridaphun Nongrum ◽  
Aiborlang Thongni ◽  
Sivaprasad Mitra ◽  
...  

An intramolecular radical cyclization reaction towards the synthesis of pyrrolidinone derivatives via metal free photoredox catalysis under blue LED irradiation has been reported. Synthetic efficiency, green reaction profile, easy isolation...


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