Literature DB >> 34910451

Green Chemistry in the Synthesis of Pharmaceuticals.

Supratik Kar1, Hans Sanderson2, Kunal Roy3,4, Emilio Benfenati4, Jerzy Leszczynski1.   

Abstract

The principles of green chemistry (GC) can be comprehensively implemented in green synthesis of pharmaceuticals by choosing no solvents or green solvents (preferably water), alternative reaction media, and consideration of one-pot synthesis, multicomponent reactions (MCRs), continuous processing, and process intensification approaches for atom economy and final waste reduction. The GC's execution in green synthesis can be performed using a holistic design of the active pharmaceutical ingredient's (API) life cycle, minimizing hazards and pollution, and capitalizing the resource efficiency in the synthesis technique. Thus, the presented review accounts for the comprehensive exploration of GC's principles and metrics, an appropriate implication of those ideas in each step of the reaction schemes, from raw material to an intermediate to the final product's synthesis, and the final execution of the synthesis into scalable industry-based production. For real-life examples, we have discussed the synthesis of a series of established generic pharmaceuticals, starting with the raw materials, and the intermediates of the corresponding pharmaceuticals. Researchers and industries have thoughtfully instigated a green synthesis process to control the atom economy and waste reduction to protect the environment. We have extensively discussed significant reactions relevant for green synthesis, one-pot cascade synthesis, MCRs, continuous processing, and process intensification, which may contribute to the future of green and sustainable synthesis of APIs.

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Year:  2021        PMID: 34910451     DOI: 10.1021/acs.chemrev.1c00631

Source DB:  PubMed          Journal:  Chem Rev        ISSN: 0009-2665            Impact factor:   60.622


  6 in total

1.  Nanomagnetic macrocyclic Schiff-base-Mn(ii) complex: an efficient heterogeneous catalyst for click approach synthesis of novel β-substitued-1,2,3-triazoles.

Authors:  Saade Abdalkareem Jasim; Yassine Riadi; Hasan Sh Majdi; Usama S Altimari
Journal:  RSC Adv       Date:  2022-06-16       Impact factor: 4.036

2.  Intermolecular Interactions and Spectroscopic Signatures of the Hydrogen-Bonded System-n-Octanol in Experimental and Theoretical Studies.

Authors:  Michał Pocheć; Katarzyna M Krupka; Jarosław J Panek; Kazimierz Orzechowski; Aneta Jezierska
Journal:  Molecules       Date:  2022-02-11       Impact factor: 4.411

3.  Synthesis and Activity of Ionic Antioxidant-Functionalized PAMAMs and PPIs Dendrimers.

Authors:  Katia Bacha; Julien Estager; Sylvie Brassart-Pasco; Catherine Chemotti; Antony E Fernandes; Jean-Pierre Mbakidi; Magali Deleu; Sandrine Bouquillon
Journal:  Polymers (Basel)       Date:  2022-08-27       Impact factor: 4.967

Review 4.  Multivalent Pyrrolidine Iminosugars: Synthesis and Biological Relevance.

Authors:  Yali Wang; Jian Xiao; Aiguo Meng; Chunyan Liu
Journal:  Molecules       Date:  2022-08-24       Impact factor: 4.927

5.  Hercynite silica sulfuric acid: a novel inorganic sulfurous solid acid catalyst for one-pot cascade organic transformations.

Authors:  Masoud Mohammadi; Arash Ghorbani-Choghamarani
Journal:  RSC Adv       Date:  2022-09-13       Impact factor: 4.036

Review 6.  GREENER Pharmaceuticals for More Sustainable Healthcare.

Authors:  Caroline T A Moermond; Neele Puhlmann; A Ross Brown; Stewart F Owen; Jim Ryan; Jason Snape; Bastiaan J Venhuis; Klaus Kümmerer
Journal:  Environ Sci Technol Lett       Date:  2022-08-23
  6 in total

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