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Heterocycles from carbenes and nitre...
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Doyle, Michael P.
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Heterocycles from carbenes and nitrenes = methods, reactions and synthetic applications /
紀錄類型:
書目-電子資源 : Monograph/item
正題名/作者:
Heterocycles from carbenes and nitrenes/ edited by Michael P. Doyle, Xinfang Xu.
其他題名:
methods, reactions and synthetic applications /
其他作者:
Doyle, Michael P.
出版者:
Cham :Springer International Publishing : : 2023.,
面頁冊數:
vii, 377 p. :ill., digital ;24 cm.
內容註:
Photo-induced Carbene Transformations to Heterocycles -- Heterocycles from Onium Ylides -- Heterocycles from Sulfur Ylides -- Heterocycles from Cascade Reactions via Carbene gem-difunctionalization -- Cyclopropanation of Heterocycles -- Heterocycles from Cycloaddition Reaction -- Alkynes as Carbene Precursors for the Synthesis of Heterocycles -- Heterocycles from Donor/Donor Carbenes -- Heterocycles by Nitrene Transfer Reactions.
Contained By:
Springer Nature eBook
標題:
Heterocyclic compounds. -
電子資源:
https://doi.org/10.1007/978-3-031-36735-9
ISBN:
9783031367359
Heterocycles from carbenes and nitrenes = methods, reactions and synthetic applications /
Heterocycles from carbenes and nitrenes
methods, reactions and synthetic applications /[electronic resource] :edited by Michael P. Doyle, Xinfang Xu. - Cham :Springer International Publishing :2023. - vii, 377 p. :ill., digital ;24 cm. - Topics in heterocyclic chemistry,v. 591861-9290 ;. - Topics in heterocyclic chemistry ;v. 59..
Photo-induced Carbene Transformations to Heterocycles -- Heterocycles from Onium Ylides -- Heterocycles from Sulfur Ylides -- Heterocycles from Cascade Reactions via Carbene gem-difunctionalization -- Cyclopropanation of Heterocycles -- Heterocycles from Cycloaddition Reaction -- Alkynes as Carbene Precursors for the Synthesis of Heterocycles -- Heterocycles from Donor/Donor Carbenes -- Heterocycles by Nitrene Transfer Reactions.
This book provides researchers in the fields of organic chemistry, organometallic chemistry and homogeneous catalysis with an overview of recent developments in the applications of reactions involving carbene and nitrene intermediates directed to the synthesis of heterocyclic compounds. Multiple pathways through which diverse heterocyclic compounds are accessed occur from a variety of carbene and nitrene precursors through C-H/X-H insertions, cycloadditions, ylide transformations, rearrangements, and cascade reactions. Catalytic processes that form metallo-carbenes and nitrenes offer unparalleled chemo-, regio-, and stereo-selectivities. Insights are provided into the scope of these methodologies and the inherent control of catalyst ligands on reaction selectivities.
ISBN: 9783031367359
Standard No.: 10.1007/978-3-031-36735-9doiSubjects--Topical Terms:
621046
Heterocyclic compounds.
LC Class. No.: QD400 / .H48 2023
Dewey Class. No.: 547.59
Heterocycles from carbenes and nitrenes = methods, reactions and synthetic applications /
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Photo-induced Carbene Transformations to Heterocycles -- Heterocycles from Onium Ylides -- Heterocycles from Sulfur Ylides -- Heterocycles from Cascade Reactions via Carbene gem-difunctionalization -- Cyclopropanation of Heterocycles -- Heterocycles from Cycloaddition Reaction -- Alkynes as Carbene Precursors for the Synthesis of Heterocycles -- Heterocycles from Donor/Donor Carbenes -- Heterocycles by Nitrene Transfer Reactions.
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This book provides researchers in the fields of organic chemistry, organometallic chemistry and homogeneous catalysis with an overview of recent developments in the applications of reactions involving carbene and nitrene intermediates directed to the synthesis of heterocyclic compounds. Multiple pathways through which diverse heterocyclic compounds are accessed occur from a variety of carbene and nitrene precursors through C-H/X-H insertions, cycloadditions, ylide transformations, rearrangements, and cascade reactions. Catalytic processes that form metallo-carbenes and nitrenes offer unparalleled chemo-, regio-, and stereo-selectivities. Insights are provided into the scope of these methodologies and the inherent control of catalyst ligands on reaction selectivities.
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