Synthesis of Chiral Tetrahydrofurans and Pyrrolidines by Visible-Light-Mediated Deoxygenation
نویسندگان
چکیده
منابع مشابه
Synthesis of Chiral Tetrahydrofurans and Pyrrolidines by Visible‐Light‐Mediated Deoxygenation
The synthesis of chiral tetrahydrofurans and pyrrolidines starting from 1,2-diols or β-amino alcohols, respectively, by visible-light-mediated deoxygenation is described. Easily accessible monoallylated/propargylated substrates were activated either as inexpensive ethyl oxalates or as recyclable 3,5-bis(trifluoromethyl)benzoates to generate alkyl radicals suitable for 5-exo-trig/5-exo-dig cycli...
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کاتالیست یک سنتز جدید برای تیواترها توصیف شده است. واکنش الکل ها با آریل، هتروآریل و آلکیل تیو ل ها درحضور 1،3،5- تری آزو- 2،4،6- تری فسفرین-2،2،4،4،6،6 هگزاکلراید ((tapc به عنوان یک کاتالیست موُثر، بازده های خوب تا عالی از تیواترها را حاصل می کند. علاوه براین، واکنش تحت شرایط بدون فلز و بدون حلال پیش می رود، بنابراین یک مکمل جالب برای روش های شناخته شده سنتز تیواترها ارائه می دهد. یک مکانیسم ا...
15 صفحه اولVisible light photoredox-catalyzed deoxygenation of alcohols
Carbon-oxygen single bonds are ubiquitous in natural products whereas efficient methods for their reductive defunctionalization are rare. In this work an environmentally benign protocol for the activation of carbon-oxygen single bonds of alcohols towards a reductive bond cleavage under visible light photocatalysis was developed. Alcohols were activated as 3,5-bis(trifluoromethyl)-substituted be...
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Carbazole, discovered over 100 years ago, is a privileged heterocyclic motif whose electronic and structural features have allowed its derivatives to find numerous applications. In addition to its abundance in natural products and bioactive molecules, carbazole has been a key motif in the development of organic light-emitting materials because of its wide band gap, high luminescent efficiency, ...
متن کاملVisible light-induced difunctionalization of electron-enriched styrenes: synthesis of tetrahydrofurans and tetrahydropyrans.
The difunctionalization of electron-enriched styrenes for the synthesis of substituted tetrahydrofurans and tetrahydropyrans in the presence of photoredox catalysts is described. The procedure is highlighted by its operational simplicity, low catalyst loadings (1 mol%), excellent stereoselectivity and mild reaction conditions.
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ژورنال
عنوان ژورنال: European Journal of Organic Chemistry
سال: 2017
ISSN: 1434-193X
DOI: 10.1002/ejoc.201700014