Bandyopadhyay Debasish, Chavez Ashlee, Banik Bimal K
Department of Chemistry, The University of Texas-Rio Grande Valley, 1201 West University Drive, Edinburg, Texas 78539, United States.
Community Health Systems of South Texas, 3135 Sugar Road, Edinburg Texas 78539, United States.
Curr Med Chem. 2017;24(41):4677-4713. doi: 10.2174/0929867324666170320121142.
Bismuth salts-mediated reactions have become a powerful tool for the synthesis of diverse medicinally-significant compounds because of their low-toxicity (non-toxic) and Lewis acidic capacity. In fact, LD50 of bismuth nitrate is lower than table salt. On the other hand, microwave-induced chemical synthesis is considered as a major greener route in modern chemistry.
A total of 139 publications (including a few authentic web links) have been reviewed mainly to discuss bismuth salts-induced electrophilic aromatic substitution, protection-deprotection chemistry of carbonyl compounds, enamination, oxidation, carbohydrate chemistry, hydrolysis, addition-elimination route, Paal-Knorr reaction, Clauson-kaas synthesis, Michael addition, aza-Michael addition, Hantzsch reaction, Biginelli reaction, Ferrier rearrangement, Pechmann condensation, Diels-Alder and aza-Diels- Alder reactions, as well as effects of microwave irradiation in a wide range of chemical transformations.
Bismuth salts-mediated reactions are developed for the synthesis of diverse organic molecules of medicinal significance. Reactions conducted with bismuth salts are environmentally benign, economical, rapid and high yielding. Microwave irradiation has accelerated these reactions significantly. It is believed that bismuth salts released corresponding acids in the media during the reaction. However, a coordination of bismuth salt to the electronegative atom is also observed in the NMR study. Bismuth has much less control (less attractive forces) over anions (for example, halides, nitrate, sulfate and triflates) compared to alkali metals. Therefore, it forms weak bond with electronegative atoms more readily and facilitates the reactions significantly. Many products obtained via bismuth salts-mediated reactions are medicinally active or intermediate for the synthesis of biologically active molecules including antifungal, anti-parasitic, anticancer and antibacterial agents, as well as agents to prevent Leishmaniosis and Chagas' diseases.
Bismuth salts are able to (i) generate mineral acids in the reaction media and (ii) coordinate with electronegative atoms to facilitate the reaction. When the reagents and the catalyst (bismuth salt) are subjected to microwave irradiation, microwave passes through the (glass) walls of the reaction vessel and heat only the reactants avoiding local overheating at the wall of the vessel. Accordingly, the possibility of side reaction and subsequent by-product formation are reduced abruptly which in turn increases the yield of the desired product. The extreme rapidity with excellent yield of the product can be rationalized as a synergistic effect of the bismuth salts and microwave irradiation.
铋盐介导的反应因其低毒性(无毒)和路易斯酸性,已成为合成多种具有重要药用价值化合物的有力工具。事实上,硝酸铋的半数致死量低于食盐。另一方面,微波诱导化学合成被认为是现代化学中一条更环保的主要途径。
共查阅了139篇文献(包括一些可靠的网页链接),主要讨论铋盐诱导的亲电芳香取代反应、羰基化合物的保护-脱保护化学、烯胺化反应、氧化反应、碳水化合物化学、水解反应、加成-消除途径、帕尔-克诺尔反应、克劳森-卡斯合成反应、迈克尔加成反应、氮杂迈克尔加成反应、汉茨希反应、贝纳利反应、费里尔重排反应、佩希曼缩合反应、狄尔斯-阿尔德反应和氮杂狄尔斯-阿尔德反应,以及微波辐射在广泛化学转化中的作用。
开发了铋盐介导的反应来合成多种具有药用意义的有机分子。用铋盐进行的反应环境友好、经济、快速且产率高。微波辐射显著加速了这些反应。据信,铋盐在反应过程中在介质中释放出相应的酸。然而,在核磁共振研究中也观察到铋盐与电负性原子的配位。与碱金属相比,铋对阴离子(例如卤化物、硝酸盐、硫酸盐和三氟甲磺酸盐)的控制作用要小得多(吸引力较小)。因此,它更容易与电负性原子形成弱键并显著促进反应。通过铋盐介导的反应获得的许多产物具有药用活性或作为合成生物活性分子(包括抗真菌剂、抗寄生虫剂、抗癌剂和抗菌剂,以及预防利什曼病和恰加斯病的药物)的中间体。
铋盐能够(i)在反应介质中产生无机酸,以及(ii)与电负性原子配位以促进反应。当试剂和催化剂(铋盐)受到微波辐射时,微波穿过反应容器的(玻璃)壁,仅加热反应物,避免容器壁局部过热。因此,副反应和随后副产物形成的可能性急剧降低,进而提高了所需产物的产率。产物极高的反应速度和优异的产率可归因于铋盐和微波辐射的协同效应。