A study of [3+2] cycloaddition reaction of hydrazonoyl chloride and β‐oxodithioester under Lewis acid catalysis: Stereoselective synthesis of (Z)‐1,3,4‐thiadiazol‐2(3H)‐ylidenes.

Author(s):  
Sridhar Madabhushi ◽  
Ramesh Kumar Chellu ◽  
Srinivas Kurva ◽  
Anil Kumar Soda ◽  
Sai Krishna Chilaka ◽  
...  
Molecules ◽  
2020 ◽  
Vol 25 (3) ◽  
pp. 692
Author(s):  
Víctor E. Macías-Villamizar ◽  
Luís Cuca-Suárez ◽  
Santiago Rodríguez ◽  
Florenci V. González

We report on the regio- and stereoselective synthesis of tetrahydrofurans by reaction between epoxides and alkenes in the presence of a Lewis acid. This is an unprecedented formal [3+2] cycloaddition reaction between an epoxide and an alkene. The chemical reaction represents a very concise synthesis of tetrahydrofurans from accessible starting compounds.


2017 ◽  
Vol 53 (82) ◽  
pp. 11353-11356 ◽  
Author(s):  
Stalin R. Pathipati ◽  
Lars Eriksson ◽  
Nicklas Selander

An indium-catalysed α,α′-annulation of cyclic ketones and alkynyl enones, leading to bicyclo[3.n.1]alkenones, is presented.


2004 ◽  
Vol 126 (17) ◽  
pp. 5366-5367 ◽  
Author(s):  
Mukund P. Sibi ◽  
Kennosuke Itoh ◽  
Craig P. Jasperse

2016 ◽  
Vol 35 (17) ◽  
pp. 2830-2835 ◽  
Author(s):  
Benjamin R. Reiner ◽  
Mark W. Bezpalko ◽  
Bruce M. Foxman ◽  
Casey R. Wade

2016 ◽  
Vol 55 (27) ◽  
pp. 7852-7856 ◽  
Author(s):  
Tim Bleith ◽  
Qing-Hai Deng ◽  
Hubert Wadepohl ◽  
Lutz H. Gade

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