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Construction and functionalization o...

Nacsa, Eric.

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Construction and functionalization of heterocycles by electrochemistry

紀錄類型:	書目-電子資源 : Monograph/item
正題名/作者:	Construction and functionalization of heterocycles by electrochemistry/ edited by Eric Nacsa ; with contributions by P. Fang ... [et al.].
其他作者:	Nacsa, Eric.
出版者:	Cham :Springer Nature Switzerland : : 2024.,
面頁冊數:	vii, 162 p. :ill. (chiefly color), digital ;24 cm.
內容註:	Construction and derivatization of indole derivatives under electrochemical conditions -- Construction and Functionalization of heterocycles via electrochemical C-H functionalization -- Recent progress in electro-oxidative cross-coupling and annulation -- Electrochemical heterocyclic ring-forming reactions by making C-N and N-N bonds -- Electrochemical (hetero)spirocyclization reactions -- Electrochemical Synthesis and Functionalization of N- and S-heterocycles -- Electrochemical annulation and functionalization of multi-nitrogen-containing heteroaromatics.
Contained By:	Springer Nature eBook
標題:	Heterocyclic compounds - Synthesis. -
電子資源:	https://doi.org/10.1007/978-3-031-74264-4
ISBN:	9783031742644

Construction and functionalization of heterocycles by electrochemistry
Construction and functionalization of heterocycles by electrochemistry[electronic resource] /edited by Eric Nacsa ; with contributions by P. Fang ... [et al.]. - Cham :Springer Nature Switzerland :2024. - vii, 162 p. :ill. (chiefly color), digital ;24 cm. - Topics in heterocyclic chemistry,v. 611861-9290 ;. - Topics in heterocyclic chemistry ;v. 61..

Construction and derivatization of indole derivatives under electrochemical conditions -- Construction and Functionalization of heterocycles via electrochemical C-H functionalization -- Recent progress in electro-oxidative cross-coupling and annulation -- Electrochemical heterocyclic ring-forming reactions by making C-N and N-N bonds -- Electrochemical (hetero)spirocyclization reactions -- Electrochemical Synthesis and Functionalization of N- and S-heterocycles -- Electrochemical annulation and functionalization of multi-nitrogen-containing heteroaromatics.

This book highlights a selection of recent electrochemical approaches to synthesize heterocyclic compounds. Electrochemistry has recently re-emerged as a prevalent technique to promote synthetic organic reactions. This renewed interest arises from its sustainability as well as its ability to engage compounds in unique ways that complement conventional chemical reagents. In the context of heterocyclic synthesis, electrochemistry enables the annulation of simple precursors and the direct functionalization and elaboration of heterocycles, which are the focus of this volume. The primary target audience includes synthetic chemists at all levels of industry and academia.

ISBN: 9783031742644

Standard No.: 10.1007/978-3-031-74264-4doiSubjects--Topical Terms:

726221
Heterocyclic compounds
--Synthesis.

LC Class. No.: QD400.5.S95

Dewey Class. No.: 547.59

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505 0 $a Construction and derivatization of indole derivatives under electrochemical conditions -- Construction and Functionalization of heterocycles via electrochemical C-H functionalization -- Recent progress in electro-oxidative cross-coupling and annulation -- Electrochemical heterocyclic ring-forming reactions by making C-N and N-N bonds -- Electrochemical (hetero)spirocyclization reactions -- Electrochemical Synthesis and Functionalization of N- and S-heterocycles -- Electrochemical annulation and functionalization of multi-nitrogen-containing heteroaromatics.
520 $a This book highlights a selection of recent electrochemical approaches to synthesize heterocyclic compounds. Electrochemistry has recently re-emerged as a prevalent technique to promote synthetic organic reactions. This renewed interest arises from its sustainability as well as its ability to engage compounds in unique ways that complement conventional chemical reagents. In the context of heterocyclic synthesis, electrochemistry enables the annulation of simple precursors and the direct functionalization and elaboration of heterocycles, which are the focus of this volume. The primary target audience includes synthetic chemists at all levels of industry and academia.
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