A new synthesis of trifluoromethyl sulfides utilizing thiocyanates and fluoroform
摘要:
Fluoroform is a potent greenhouse gas which should not be released to the atmosphere. Large amounts of it are stored and wait for new and useful reactions to be based on it. One such general reaction that is described in this paper is its use in preparation of the important organic trifluoromethyl sulfides. Aliphatic, aromatic and heterocyclic thiocyanates are easy to prepare. They were reacted with fluoroform-based CuCF3 to form the corresponding (trifluoromethyl)thio derivatives. (C) 2014 Elsevier B.V. All rights reserved.
COMPOUNDS WITH COPPER- OR ZINC-ACTIVATED TOXICITY AGAINST MICROBIAL INFECTION
申请人:Kansas State University Research Foundation
公开号:US20220024877A1
公开(公告)日:2022-01-27
Heterocyclic compounds with a novel pyrazole thioamide-based NNSN structural motif, having highly effective zinc- or copper-activated toxicity against microbial infections at micromolar or nanomolar minimum inhibitory concentrations (MIC), and methods of making and using same.
세미카바자이드 유도체 화합물 또는 이의 약학적으로 허용가능한 염을 포함하는 프리온 질환의 예방 또는 치료용 약학적 조성물
申请人:한양대학교 에리카산학협력단
公开号:KR20230066192A
公开(公告)日:2023-05-15
본 발명은 세미카바자이드 유도체 또는 이의 약학적으로 허용가능한 염을 유효성분으로 포함하는 프리온 질환의 예방 또는 치료용 약학적 조성물에 관한 것으로, 화학식 1로 표시되는 세미카바자이드 유도체 또는 이의 약학적으로 허용가능한 염은 프리온 단백질의 응집을 억제하는 효과가 탁월하여 프리온 단백질 PrPsc의 응집체가 야기하는 질환의 예방 및 치료용 약물로서 유용하게 사용될 수 있다.
Effects of solvation on the nucleophilic reaction of stable carbanions with diaryl disulfides
作者:H. F. Gilbert
DOI:10.1021/ja00543a028
日期:1980.11
Reaction of Aromatic Thiocyanates with Trialkyl Phosphites
作者:Kurt Pilgram、Donald D. Phillips
DOI:10.1021/jo01018a067
日期:1965.7
[EN] COMPOUNDS WITH COPPER- OR ZINC-ACTIVATED TOXICITY AGAINST MICROBIAL INFECTION<br/>[FR] COMPOSÉS PRÉSENTANT UNE TOXICITÉ ACTIVÉE PAR DU CUIVRE OU DU ZINC CONTRE UNE INFECTION MICROBIENNE
申请人:UNIV KANSAS STATE
公开号:WO2020061412A1
公开(公告)日:2020-03-26
Heterocyclic compounds with a novel pyrazole thioamide-based NNSN structural motif, having highly effective zinc- or copper-activated toxicity against microbial infections at micromolar or nanomolar minimum inhibitory concentrations (MIC), and methods of making and using the same.