101835-24-9Relevant articles and documents
Isocyanide-based multicomponent reaction for the formation of 1,3-oxathiolane-2-imine derivatives
Samzadeh-Kermani, Alireza,Zamenraz, Samira
, p. 1753 - 1760 (2017)
Abstract: The adduct of isocyanide and elemental sulfur has been employed as the isothiocyanate source in reaction with oxirane to form 1,3-oxathiolane-2-imine derivatives. The optimum conditions are developed using HMPA at 55?°C for 12?h. Various isocyan
Oxime-catalyzed formation of functionalized 1,3-oxathiolanes from aryl isothiocyanates and oxiranes
Yavari, Issa,Ghazanfarpour-Darjani, Majid
, p. 477 - 483 (2014/08/18)
An efficient synthesis of N-(5-alkyl-1,3-oxathiolan-2-ylidene)arylamines via a one-pot reaction between arylisothiocyanates and substituted oxiranes in the presence of catalytic amount of pyridine-2-carbaldehyde oxime is described.
A new facile synthetic method for the construction of 1,3-oxathiolan-2-ylidenes
Ghosh, Harisadhan,Singh,Murru, Siva,Kavala, Veerababurao,Patel, Bhisma K.
, p. 2602 - 2606 (2008/09/18)
A new, convenient and efficient synthetic method for the construction of 1,3-oxathiolan-2-ylidenes via sodium borohydride reduction of the addition product of dithiocarbamic acid esters with α-bromoketones under basic conditions is reported. This method is general and applicable to a range of systems.
