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      Development of a Continuous Flow Baldwin Rearrangement Process and Its Comparison to Traditional Batch Mode

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          Abstract

          A new and highly efficient continuous flow process is presented for the synthesis of aziridines via the thermal Baldwin rearrangement. The process was initially explored using traditional batch synthesis techniques but suffered from moderate yields, long reaction times, and moderate diastereoselectivities. Here we demonstrate that the process can be greatly improved upon its transfer to continuous flow, which afforded the aziridine targets in high yields, short reaction times, and consistently high diastereoselectivities, with the high-throughput process rendering multigram quantities of product in short periods of time. In addition, flow processing extended the substrate scope including several examples that had failed in batch mode, thus demonstrating the value of this overlooked entry into valuable aziridine species.

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          The Hitchhiker's Guide to Flow Chemistry ∥.

          Flow chemistry involves the use of channels or tubing to conduct a reaction in a continuous stream rather than in a flask. Flow equipment provides chemists with unique control over reaction parameters enhancing reactivity or in some cases enabling new reactions. This relatively young technology has received a remarkable amount of attention in the past decade with many reports on what can be done in flow. Until recently, however, the question, "Should we do this in flow?" has merely been an afterthought. This review introduces readers to the basic principles and fundamentals of flow chemistry and critically discusses recent flow chemistry accounts.
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            Modern advances in heterocyclic chemistry in drug discovery

            New advances in functionalized heterocyclic chemistry are of critical importance to the medicinal chemist as it provides the ability to expand the available drug-like chemical space and drive more efficient delivery of drug discovery programs. New advances in synthetic methodologies that allow rapid access to a wide variety of functionalized heterocyclic compounds are of critical importance to the medicinal chemist as it provides the ability to expand the available drug-like chemical space and drive more efficient delivery of drug discovery programs. Furthermore, the development of robust synthetic routes that can readily generate bulk quantities of a desired compound help to accelerate the drug development process. While established synthetic methodologies are commonly utilized during the course of a drug discovery program, the development of innovative heterocyclic syntheses that allow for different bond forming strategies are having a significant impact in the pharmaceutical industry. This review will focus on recent applications of new methodologies in C–H activation, photoredox chemistry, borrowing hydrogen catalysis, multicomponent reactions, regio- and stereoselective syntheses, as well as other new, innovative general syntheses for the formation and functionalization of heterocycles that have helped drive project delivery. Additionally, the importance and value of collaborations between industry and academia in shaping the development of innovative synthetic approaches to functionalized heterocycles that are of greatest interest to the pharmaceutical industry will be highlighted.
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              Aziridines: epoxides’ ugly cousins?

              J Sweeney (2002)
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                Author and article information

                Journal
                Org Process Res Dev
                Org Process Res Dev
                op
                oprdfk
                Organic Process Research & Development
                American Chemical Society
                1083-6160
                1520-586X
                11 September 2023
                17 May 2024
                : 28
                : 5 , Flow Chemistry Enabling Efficient Synthesis 2024
                : 1567-1575
                Affiliations
                []School of Chemistry, University College Dublin , Science Centre South, Belfield, Dublin 4, Ireland D04 N2E2
                Author notes
                Author information
                https://orcid.org/0000-0002-6996-5893
                Article
                10.1021/acs.oprd.3c00213
                11110046
                38783852
                f1689dbc-5c74-43c8-8d6f-62f6cf81bb82
                © 2023 The Authors. Published by American Chemical Society

                Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained ( https://creativecommons.org/licenses/by/4.0/).

                History
                : 04 July 2023
                Funding
                Funded by: Science Foundation Ireland, doi 10.13039/501100001602;
                Award ID: 12/RC2275_P2
                Funded by: Irish Research Council, doi 10.13039/501100002081;
                Award ID: GOIPG/2020/1177
                Funded by: Science Foundation Ireland, doi 10.13039/501100001602;
                Award ID: 20/FFP-P/8712
                Funded by: Science Foundation Ireland, doi 10.13039/501100001602;
                Award ID: 18/RI/5702
                Categories
                Article
                Custom metadata
                op3c00213
                op3c00213

                aziridine,baldwin rearrangement,flow chemistry,high throughput,scale-up

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