In situ generation and intramolecular trapping of o-xylylenes by cobalt-catalyzed acetylene cooligomerizations. A one-step synthesis of polycycles

1976 ◽  
Vol 98 (21) ◽  
pp. 6755-6757 ◽  
Author(s):  
Raymond L. Funk ◽  
K. Peter C. Vollhardt
Keyword(s):  
One Step ◽  
2017 ◽  
Vol 12 (6) ◽  
pp. 1934578X1701200
Author(s):  
Kazuaki Shimada ◽  
Fumiya Ishikawa ◽  
Md. Ashraful Alam ◽  
Toshinobu Korenaga

Treatment of substituted propargyl methyl ethers with a base and elemental sulfur in the presence of a thiolate ion afforded 2-alkenecarbodithioate esters in good yields. The reaction is assumed to proceed through a pathway involving in situ generation of propadienethione intermediates. Further conversion of 2-alkenecarbodithioate esters into 2,3-dihydroisothiazoles were efficiently performed by treating with chloramine-T through a [4+1] type oxidative ring closure via thiocarbonyl S-tosylimides.


2019 ◽  
Vol 7 (9) ◽  
pp. 4446-4450 ◽  
Author(s):  
Xinyao Shan ◽  
Ning Sui ◽  
Wengang Liu ◽  
Manhong Liu ◽  
Jian Liu

A one-step in situ route to obtain well-defined and size-controllable Pd nanoparticles was reported and employed for catalytic applications.


2019 ◽  
Vol 9 (18) ◽  
pp. 5142-5149
Author(s):  
Amin Delparish ◽  
Shamayita Kanungo ◽  
John van der Schaaf ◽  
M. Fernanda Neira d'Angelo

This study aims to shed light on the one-step oxidation of methane to methanol with in situ generated H2O2 by means of a wall-coated catalytic microreactor.


RSC Advances ◽  
2016 ◽  
Vol 6 (19) ◽  
pp. 15430-15440 ◽  
Author(s):  
Christian Steinebach ◽  
Anna-Christina Schulz-Fincke ◽  
Gregor Schnakenburg ◽  
Michael Gütschow

The proton-catalyzed transformation of 2-thioureidobenzonitriles in the presence of acyl donors provides a convenient one-step entry to 4-acylimino-4H-3,1-benzothiazines.


Author(s):  
Kazumasa Funabiki ◽  
Toshiya Gotoh ◽  
Ryunosuke Kani ◽  
Toshiyasu Inuzuka ◽  
Yasuhiro Kubota

A highly diastereo- and enantioselective organocatalytic method to synthesise erythritols bearing a trifluoromethyl group has been investigated.


2020 ◽  
Vol 24 ◽  
Author(s):  
Wengui Wang ◽  
Shoufeng Wang

Abstract:: Minisci-type reactions have become widely known as reactions that involve the addition of carbon-centered radicals to basic heteroarenes followed by formal hydrogen atom loss. While the originally developed protocols for radical generation remain in active use today, in recent years by a new array of radical generation strategies allow use of a wider variety of radical precursors that often operate under milder and more benign conditions. New transformations based on free radical reactivity are now available to a synthetic chemist looking to utilize a Minisci-type reaction. Radical-generation methods based on photoredox catalysis and electrochemistry, which utilize thermal cleavage or the in situ generation of reactive radical precursors, have become popular approaches. Our review will cover the remarkably literature that has appeared on this topic in recent 5 years, from 2015-01 to 2020-01, in an attempt to provide guidance to the synthetic chemist, on both the challenges that have been overcome and applications in organic synthesis.


2021 ◽  
Author(s):  
Thomas Richards ◽  
Jonathan H. Harrhy ◽  
Richard J. Lewis ◽  
Alexander G. R. Howe ◽  
Grzegorz M. Suldecki ◽  
...  

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