Sustainable Synthesis of Medicinally Important Heterocycles.

IF 3.3 3区 医学 Q2 CHEMISTRY, MEDICINAL
Dripta De Joardar, Rajarshi Sarkar, Dilip K Maiti
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引用次数: 0

Abstract

Sustainable chemistry and nature-friendly protocols are not only luxury but has become essential requirement for the modern society as it progresses towards a more responsible future. To match the current needs of the community, industries and in particular chemical industry is looking for novel and cheap strategies that have less adverse effects on the environment. Heterocyclic compounds are one particular motif, which is prevalent in nature. It is found in a wide range of synthetic and natural compounds, both established and in development as potent therapeutic candidates. According to the US retail market in 2014-2015, heterocyclic moieties constitute the basic skeletons for 80% of marketed pharmaceuticals. However, majority of the synthetic methodologies still uses classical approaches with toxic solvents, stoichiometric reagents, reactions with less atom economy etc. Thus, there is an urgent need for green, sustainable alternatives of the classical reactions. In recent years, an array of diverse approaches and technologies have been discovered by the scientific community to address the issue of eco-friendly manufacture of various pharmaceutically and medicinally important heterocyclic molecules. In this context, the current review will summarize various reported green pathways to the heterocyclic architecture, particularly O, N, and S-heterocyclic compounds. The methods highlighted in this article includes reaction in environment friendly nonconventional media, solvent-free approaches, heterogeneous catalysis, organocatalysis, electrochemical reactions, microwave-mediated reactions, ultrasound-based reactions, enzymatic reactions, biocatalysis, and others.

药用重要杂环化合物的可持续合成。
可持续化学和自然友好型协议不仅是奢侈品,而且已经成为现代社会的基本要求,因为它朝着更负责任的未来发展。为了配合社会目前的需要,工业,特别是化学工业正在寻找对环境不利影响较小的新颖和廉价的战略。杂环化合物是自然界中普遍存在的一种特殊基序。它存在于广泛的合成和天然化合物中,无论是已经建立的还是正在开发的强有力的治疗候选者。根据2014-2015年美国零售市场的数据,杂环部分构成了80%上市药品的基本骨架。然而,大多数的合成方法仍然采用经典的方法,使用有毒溶剂、化学计量试剂、原子经济性差的反应等。因此,迫切需要绿色,可持续的替代经典反应。近年来,科学界已经发现了一系列不同的方法和技术来解决各种具有重要药用价值的杂环分子的生态制造问题。在此背景下,本综述将总结各种报道的绿色途径,特别是O, N和s杂环化合物。本文重点介绍的方法包括在环境友好型非常规介质中的反应、无溶剂方法、多相催化、有机催化、电化学反应、微波介导反应、超声反应、酶促反应、生物催化等。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.80
自引率
0.00%
发文量
231
审稿时长
6 months
期刊介绍: The aim of Mini-Reviews in Medicinal Chemistry is to publish short reviews on the important recent developments in medicinal chemistry and allied disciplines. Mini-Reviews in Medicinal Chemistry covers all areas of medicinal chemistry including developments in rational drug design, synthetic chemistry, bioorganic chemistry, high-throughput screening, combinatorial chemistry, drug targets, and natural product research and structure-activity relationship studies. Mini-Reviews in Medicinal Chemistry is an essential journal for every medicinal and pharmaceutical chemist who wishes to be kept informed and up-to-date with the latest and most important developments.
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