708-94-1Relevant articles and documents
Microwave-assisted reactions of α-diazoketones with hetaryl and ferrocenyl thioketones*
Mlostoń, Grzegorz,Hamera-Fa?dyga, Ró?a,Jeske, Ma?gorzata,Godziszewska, Magdalena,Urbaniak, Katarzyna,Heimgartner, Heinz
, p. 47 - 63 (2018)
Differently substituted hetaryl thioketones react with less reactive diazoketones under microwave (MW) irradiation in toluene solution. After only 2 min, the reactions were complete and, depending on the type of the used diazoketone, α,β-unsaturated keton
-Annulation of Azaoxyallyl Cations and Thiocarbonyls for the Assembly of Thiazolidin-4-ones
Jaiswal, Vandana,Mondal, Biplab,Singh, Kuldeep,Das, Dinabandhu,Saha, Jaideep
supporting information, p. 5848 - 5852 (2019/08/26)
A base-promoted, efficient [3 + 2] annulation between azaoxyallyl cations and thiocarbonyls is reported for flexible access to highly functionalized thiazolidin-4-one derivatives in good to excellent yields. An intriguing feature of this method is the met
Thia-Diels–Alder reactions of hetaryl thioketones with nonactivated 1,3-dienes leading to 3,6-dihydro-2H-pyrans: evidence for a diradical mechanism
Mlostoń, Grzegorz,Grzelak, Paulina,Linden, Anthony,Heimgartner, Heinz
, p. 518 - 525 (2017/08/30)
[Figure not available: see fulltext.] Dihetaryl thioketones possessing thiophen-2-yl and selenophen-2-yl rings react as “superdienophilic” reagents with nonactivated 1,3-dienes such as 2,3-dimethylbuta-1,3-diene, cyclopentadiene, and mixtures of isomeric
