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Titlebook: Development of a New Heterocycle-Forming Reaction and Kinetic Resolution with N-Heterocyclic Carbene; Yinli Wang Book 2019 Springer Nature

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發(fā)表于 2025-3-21 16:24:47 | 只看該作者 |倒序瀏覽 |閱讀模式
書目名稱Development of a New Heterocycle-Forming Reaction and Kinetic Resolution with N-Heterocyclic Carbene
編輯Yinli Wang
視頻videohttp://file.papertrans.cn/271/270014/270014.mp4
概述Nominated as an outstanding PhD thesis by Kyoto University.Provides comprehensive information on N-heterocyclic carbenes.Offers practical guidance on the design and optimization of catalytic reaction
叢書名稱Springer Theses
圖書封面Titlebook: Development of a New Heterocycle-Forming Reaction and Kinetic Resolution with N-Heterocyclic Carbene;  Yinli Wang Book 2019 Springer Nature
描述.In this book, the author focuses on exploring new organocatalytic transformations under operationally simple and environmentally friendly reaction conditions. Two new types of catalytic reactions promoted by N-heterocyclic carbenes (NHCs) are described. The oxa- and azacycle-forming reactions of sulfonylalkynols and sulfonylalkynamides are broadly considered to be a new type of activation mode in NHC chemistry, wherein the bond formation with internal O- and N-nucleophiles occurs at the γ-position of the propargyl sulfones with 1,2-sulfonyl migration. The resulting oxa- and azacycles are core structures in many biologically significant compounds and medicinally important agents.?.In addition, the book develops the chiral NHC-catalyzed kinetic resolution of α-hydroxy carboxylic acid derivatives based on chiral recognition of the substrate–cocatalyst complex. In this carboxylate cocatalyst-assisted chiral acylation, the reaction rate acceleration and selectivity enhancementare interpreted in terms of the reversible complexation of the substrate and carboxylate cocatalyst, which is verified by control experiments and measured using analytical methods. The findings described here reve
出版日期Book 2019
關鍵詞Chiral Recognition; N-heterocyclic Carbine; Heterocycle Formation; Kinetic Resolution; Chiral Recognitio
版次1
doihttps://doi.org/10.1007/978-981-13-9398-3
isbn_softcover978-981-13-9400-3
isbn_ebook978-981-13-9398-3Series ISSN 2190-5053 Series E-ISSN 2190-5061
issn_series 2190-5053
copyrightSpringer Nature Singapore Pte Ltd. 2019
The information of publication is updating

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沙發(fā)
發(fā)表于 2025-3-21 22:45:38 | 只看該作者
Oxa- and Azacycle-Formation via Migrative Cyclization of Sulfonylalkynol and Sulfonylalkynamide,ompanied 1,2-migration of the sulfonyl groups. This reaction provides a novel access to oxa- and azacycles possessing a pendant vinyl sulfone functionality, which in turn is amenable to further transformations. During research on this migrative cyclization, mechanism studies indicated that nucleophi
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2190-5053 interpreted in terms of the reversible complexation of the substrate and carboxylate cocatalyst, which is verified by control experiments and measured using analytical methods. The findings described here reve978-981-13-9400-3978-981-13-9398-3Series ISSN 2190-5053 Series E-ISSN 2190-5061
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發(fā)表于 2025-3-22 13:11:54 | 只看該作者
Development of a New Heterocycle-Forming Reaction and Kinetic Resolution with N-Heterocyclic Carbene
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Oxa- and Azacycle-Formation via Migrative Cyclization of Sulfonylalkynol and Sulfonylalkynamide,les other than NHCs might also induce this transformation. Further investigations showed that a catalytic amount of phosphine or 4-(.-dimethylamino)pyridine (DMAP) also promoted migrative cyclization in an a. Umpolung manner similarly. Furthermore, asymmetric induction was observed when a chiral DMAP derivative was used in the reaction.
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