Construction of 6H-benzo[c]thiochromenes via a tandem reaction of arynes with thionoesters

2021 ◽  
Author(s):  
Yi An ◽  
Fang Zhang ◽  
Guangfen Du ◽  
Zhihua Cai ◽  
Lin He
Keyword(s):  
Transition Metal ◽  
Tandem Reaction ◽  
Tandem Reactions ◽  
Metal Free

A mild and transition-metal free method has been proposed for the synthesis of 6H-benzo[c]thiochromenes via the tandem reactions of arynes with thionoesters.

Transition metal-free approach to azafluoranthene scaffolds by aldol condensation/[1+2+3] annulation tandem reaction of isocyanoacetates with 8-(alkynyl)-1-naphthaldehydes

2021 ◽  
Author(s):  
Penghui Dong ◽  
Kashif Majeed ◽  
lingna Wang ◽  
Zijian Guo ◽  
Fengtao Zhou ◽  
...  
Keyword(s):  
Transition Metal ◽  
Aldol Condensation ◽  
Domino Reaction ◽  
Tandem Reaction ◽  
Metal Free ◽  
Successive Formation ◽  
General Synthesis

A transition metal-free aldol condensation/[1+2+3] annulation reaction of isocyanoacetates with 8-(alkynyl)-1-naphthaldehydes has been developed for the general synthesis of azafluoranthenes. This domino reaction enables successive formation of three new bonds...

Application of primary halogenated hydrocarbons for the synthesis of 3-aryl and 3-alkyl indolizines

2017 ◽  
Vol 15 (23) ◽  
pp. 5016-5024 ◽  
Author(s):  
Yan Liu ◽  
Huayou Hu ◽  
Junyu Zhou ◽  
Wenhui Wang ◽  
Youliang He ◽  
...  
Keyword(s):  
Transition Metal ◽  
Halogenated Hydrocarbons ◽  
Tandem Reaction ◽  
Synthetic Route ◽  
Metal Free ◽  
First Time

A transition-metal-free synthetic route to 3-aryl and 3-alkyl indolizines from electron-deficient alkenes, pyridines and primary halogenated hydrocarbons is reported for the first time using a tandem reaction.

ChemInform Abstract: An Efficient, Transition-Metal-Free Process for the Synthesis of Substituted Dihydrofurans via a Michael/Cyclization Tandem Reaction.

ChemInform ◽  
2011 ◽  
Vol 42 (20) ◽  
pp. no-no
Author(s):  
Ming-Yu Wu ◽  
Ming-Qi Wang ◽  
Kun Li ◽  
Xing-Wen Feng ◽  
Ting He ◽  
...  
Keyword(s):  
Transition Metal ◽  
Tandem Reaction ◽  
Metal Free ◽  
Free Process

New routes for the synthesis of fused pyrrole scaffolds through transition metal-free tandem reactions

2013 ◽  
Vol 54 (45) ◽  
pp. 5994-5997 ◽  
Author(s):  
Bingchuan Yang ◽  
Zixiao Huang ◽  
Hegen Guan ◽  
Xiaoyi Niu ◽  
Yanqiu Li ◽  
...  
Keyword(s):  
Transition Metal ◽  
Tandem Reactions ◽  
Metal Free

An efficient, transition-metal-free process for the synthesis of substituted dihydrofurans via a Michael/cyclization tandem reaction

2011 ◽  
Vol 52 (6) ◽  
pp. 679-683 ◽  
Author(s):  
Ming-Yu Wu ◽  
Ming-Qi Wang ◽  
Kun Li ◽  
Xing-Wen Feng ◽  
Ting He ◽  
...  
Keyword(s):  
Transition Metal ◽  
Tandem Reaction ◽  
Metal Free ◽  
Free Process

ChemInform Abstract: New Routes for the Synthesis of Fused Pyrrole Scaffolds Through Transition Metal-Free Tandem Reactions.

ChemInform ◽  
2014 ◽  
Vol 45 (10) ◽  
pp. no-no
Author(s):  
Bingchuan Yang ◽  
Zixiao Huang ◽  
Hegen Guan ◽  
Xiaoyi Niu ◽  
Yanqiu Li ◽  
...  
Keyword(s):  
Transition Metal ◽  
Tandem Reactions ◽  
Metal Free

Transition-metal-free catalytic hydroboration reduction of amides to amines

2020 ◽  
Vol 7 (21) ◽  
pp. 3515-3520
Author(s):  
Wubing Yao ◽  
Jiali Wang ◽  
Aiguo Zhong ◽  
Shiliang Wang ◽  
Yinlin Shao
Keyword(s):  
Transition Metal ◽  
Selective Catalytic Reduction ◽  
Catalytic Reduction ◽  
Value Added ◽  
Metal Free

The selective catalytic reduction of amides to value-added amine products is a desirable but challenging transformation.

Deaminative carbonylative thioesterification of activated alkylamines with thiophenols under transition-metal-free conditions

2021 ◽  
Author(s):  
Fengqian Zhao ◽  
Xiao-Feng Wu
Keyword(s):  
Free Radical ◽  
Transition Metal ◽  
Metal Free

A transition-metal-free radical carbonylation of activated alkylamines with thiophenols has been successfully developed. Various thioesters were selectively produced with moderate to good yields.

Regioselective C3-H Trifluoromethylation of 2H-Indazole Under Transition-Metal-Free Photoredox Catalysis

2019 ◽  
Author(s):  
Arumugavel Murugan ◽  
Venkata Nagarjuna Babu ◽  
Nagaraj Sabarinathan ◽  
Sharada Duddu. S
Keyword(s):  
Transition Metal ◽  
Visible Light ◽  
Practical Approach ◽  
Hypervalent Iodine ◽  
Radical Mechanism ◽  
Photoredox Catalysis ◽  
Metal Free

Here we report a visible-light-promoted metal-free regioselective C3-H trifluoromehtylation reaction that proceeds via radical mechanism and which supported by control experiments. The combination of photoredox catalysis and hypervalent iodine reagent provides a practical approach for the present trifluoromethylation reaction and synthesis of a library of trifluoromethylated indazoles.

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