23080-22-0Relevant articles and documents
Synthesis of Thioethers Using Triethylamine-Activated Phosphorus Decasulfide (P410
Turkoglu, Gulsen,Cinar, M. Emin,Ozturk, Turan
, p. 3618 - 3624 (2016/10/17)
The synthesis of thioethers in excellent yields was achieved under mild conditions via the displacement reaction of halogens by sulfur. The cross-reaction of 2-(α-bromoacetyl)thiophene with triethylamine-activated phosphorus decasulfide (Et3N-P2S5) was elaborated by utilizing DFT calculations.
Stereoselective synthesis of cis-2,6-disubstituted morpholines and 1,4-oxathianes by intramolecular reductive etherification of 1,5-diketones
Gharpure, Santosh J.,Anuradha, Dandela,Prasad, Jonnalagadda V. K.,Rao, Pidugu Srinivasa
, p. 86 - 90 (2015/01/16)
A simple and efficient, Lewis acid catalysed reductive etherification strategy for the stereoselective synthesis of cis-2,6- disubstituted morpholines and 1,4-oxathianes starting from readily available 1,5-diketones has been developed. The strategy is used in the total synthesis of morpholine-based natural products (±)-chelonin A and formal total synthesis of (±)-chelonin C.
An aquatic pseudo-four-component reaction for the synthesis of highly substituted thiophenes
Zali-Boeini, Hassan,Ghani, Maryam
, p. 913 - 918 (2013/05/08)
A novel and simple procedure was developed for the construction of fully substituted thiophenes. A series of α-haloacetophenone derivatives were converted into fully substituted thiophenes by treatment with sodium sulfide in the presence of 1,8-diazabicyc