Abstract:It is well known that heterocycles are among the most significant molecules for everyday life, ranging from natural products and bioactive substances to functional materials. This review will focus on the synthesis of heterocycles by reactions involving elemental sulfur published from 2017 until now.
“…On basis of these preliminary studies and previous reports, [21][22][23][24][25][26][27][28] a plausible pathway for the preparation of 2a from (E)-N 0 -benzylideneacetohydrazide is proposed in (Scheme 3). Initially, Ag 2 CO 3 react with 1 to produce the intermediate (A).…”
Herein we report an oxidative coupling reaction for N–S/S–S bond formation substituted N,N′-disulfanediyl bis(N′-((E)-benzylidene)acetohydrazide). It provides a direct approach for the synthesis of disulfides with good yields.
“…On basis of these preliminary studies and previous reports, [21][22][23][24][25][26][27][28] a plausible pathway for the preparation of 2a from (E)-N 0 -benzylideneacetohydrazide is proposed in (Scheme 3). Initially, Ag 2 CO 3 react with 1 to produce the intermediate (A).…”
Herein we report an oxidative coupling reaction for N–S/S–S bond formation substituted N,N′-disulfanediyl bis(N′-((E)-benzylidene)acetohydrazide). It provides a direct approach for the synthesis of disulfides with good yields.
“…Although there are a number of reviews dedicated to various aspects of the synthesis of sulphur-containing polymers and low-molecular-weight heterocyclic compounds, 2,27,[62][63][64][65][66][67] until present there have been no studies examining the inclusion of S 8 into macromolecules from both the reaction mechanisms viewpoint and in the context of the opportunities for green development of this area of research. Therefore, the present review looks into the reaction mechanisms that lead to the inclusion of elemental sulphur into polymers and discusses the opportunities for the implementation of such processes under conditions that comply with the principles of green chemistry.…”
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