Sulfonyl halide synthesis by thiol oxyhalogenation using NBS/NCS – i PrOH
作者:Carolina Silva-Cuevas、Carlos Perez-Arrieta、Luis A. Polindara-García、J. Armando Lujan-Montelongo
DOI:10.1016/j.tetlet.2017.04.087
日期:2017.6
A rapid and facile method provides a general route to sulfonyl bromides/chlorides by the oxidation of thiols using NXS – ROH (X = Br,Cl, R = iPr) as an oxyhalogenation reagent. Control experiments suggest that the alcohol component is the source of oxygen. The proposed method enable the access to structurally diverse sulfonyl bromides and chlorides including challenging examples, inaccessible by other
一种快速而简便的方法,是使用NXS – ROH(X = Br,Cl,R = i Pr)作为氧卤代试剂氧化硫醇,从而提供了磺酰溴/氯化物的一般途径 。对照实验表明,酒精成分是氧气的来源。所提出的方法使得能够获得结构上不同的磺酰溴和氯化物,包括具有挑战性的实例,这是其他合成方法所无法达到的。
Benzenesulphonamidoindanyl compounds
申请人:Dr. Karl Thomae GmbH
公开号:US04929754A1
公开(公告)日:1990-05-29
The invention relates to new benzenesulphonamidoindanyl compounds useful in the treatment and prophylaxis of thromboembolic diseases, arteriosclerosis and tumor metastasis.
该发明涉及新的苯磺酰胺基印丹基化合物,可用于治疗和预防血栓栓塞性疾病、动脉硬化和肿瘤转移。
US4820705A
申请人:——
公开号:US4820705A
公开(公告)日:1989-04-11
US4929754A
申请人:——
公开号:US4929754A
公开(公告)日:1990-05-29
Benzenesulphonamidoindanyl compounds, medicaments thereof, and processes
申请人:Dr. Karl Thomae GmbH
公开号:US04820705A1
公开(公告)日:1989-04-11
The invention relates to new benzenesulphonamidoindanyl compounds having the following formula ##STR1## wherein the substituents are defined herein useful in the treatment and prophylaxis of thromboembolic diseases, arteriosclerosis and tumor metastasis.