Reactions of secondary propargylamines with heteroallenes for the synthesis of diverse heterocycles

Handle URI:
http://hdl.handle.net/10754/627465
Title:
Reactions of secondary propargylamines with heteroallenes for the synthesis of diverse heterocycles
Authors:
Peshkov, Vsevolod A. ( 0000-0001-6649-2384 ) ; Pereshivko, Olga P.; Nechaev, Anton A.; Peshkov, Anatoly A.; Van der Eycken, Erik V. ( 0000-0001-5172-7208 )
Abstract:
This focused review aims to summarize recent developments in the processes involving additions of secondary propargylamines to various heteroallenes and subsequent transition metal-catalyzed or electrophile-mediated cyclizations. The utility of this convenient and tunable strategy spans from the carbon dioxide fixation and target-oriented synthesis of complex natural and biologically active products to the generation of extended synthetic libraries of diverse oxygen-, nitrogen- and sulfur-containing heterocycles. For comparative purposes, the analogous transformations of propargylic alcohols are also highlighted in this account.
KAUST Department:
KAUST Catalysis Center (KCC)
Citation:
Peshkov VA, Pereshivko OP, Nechaev AA, Peshkov AA, Van der Eycken EV (2018) Reactions of secondary propargylamines with heteroallenes for the synthesis of diverse heterocycles. Chemical Society Reviews. Available: http://dx.doi.org/10.1039/c7cs00065k.
Publisher:
Royal Society of Chemistry (RSC)
Journal:
Chemical Society Reviews
Issue Date:
16-Mar-2018
DOI:
10.1039/c7cs00065k
Type:
Article
ISSN:
0306-0012; 1460-4744
Sponsors:
Support was provided by the Startup Fund from Soochow University (grant Q410900714), the Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD), the Project of Scientific and Technologic Infrastructure of Suzhou (grant SZS201708), the Fund for Scientific Research-Flanders (FWO), the Research Fund of the University of Leuven (KU Leuven) and by the Ministry of Education and Science of the Russian Federation (the agreement number 02.a03.0008). A. A. N. is grateful to the European Community Mobility Program “Erasmus Mundus Action 2, Strand 1”.
Additional Links:
http://pubs.rsc.org/en/content/articlehtml/2018/cs/c7cs00065k
Appears in Collections:
Articles; KAUST Catalysis Center (KCC)

Full metadata record

DC FieldValue Language
dc.contributor.authorPeshkov, Vsevolod A.en
dc.contributor.authorPereshivko, Olga P.en
dc.contributor.authorNechaev, Anton A.en
dc.contributor.authorPeshkov, Anatoly A.en
dc.contributor.authorVan der Eycken, Erik V.en
dc.date.accessioned2018-04-15T07:13:36Z-
dc.date.available2018-04-15T07:13:36Z-
dc.date.issued2018-03-16en
dc.identifier.citationPeshkov VA, Pereshivko OP, Nechaev AA, Peshkov AA, Van der Eycken EV (2018) Reactions of secondary propargylamines with heteroallenes for the synthesis of diverse heterocycles. Chemical Society Reviews. Available: http://dx.doi.org/10.1039/c7cs00065k.en
dc.identifier.issn0306-0012en
dc.identifier.issn1460-4744en
dc.identifier.doi10.1039/c7cs00065ken
dc.identifier.urihttp://hdl.handle.net/10754/627465-
dc.description.abstractThis focused review aims to summarize recent developments in the processes involving additions of secondary propargylamines to various heteroallenes and subsequent transition metal-catalyzed or electrophile-mediated cyclizations. The utility of this convenient and tunable strategy spans from the carbon dioxide fixation and target-oriented synthesis of complex natural and biologically active products to the generation of extended synthetic libraries of diverse oxygen-, nitrogen- and sulfur-containing heterocycles. For comparative purposes, the analogous transformations of propargylic alcohols are also highlighted in this account.en
dc.description.sponsorshipSupport was provided by the Startup Fund from Soochow University (grant Q410900714), the Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD), the Project of Scientific and Technologic Infrastructure of Suzhou (grant SZS201708), the Fund for Scientific Research-Flanders (FWO), the Research Fund of the University of Leuven (KU Leuven) and by the Ministry of Education and Science of the Russian Federation (the agreement number 02.a03.0008). A. A. N. is grateful to the European Community Mobility Program “Erasmus Mundus Action 2, Strand 1”.en
dc.publisherRoyal Society of Chemistry (RSC)en
dc.relation.urlhttp://pubs.rsc.org/en/content/articlehtml/2018/cs/c7cs00065ken
dc.titleReactions of secondary propargylamines with heteroallenes for the synthesis of diverse heterocyclesen
dc.typeArticleen
dc.contributor.departmentKAUST Catalysis Center (KCC)en
dc.identifier.journalChemical Society Reviewsen
dc.contributor.institutionCollege of Chemistry, Chemical Engineering and Materials Science, Dushu Lake Campus, Soochow University, Suzhou 215123, China.en
dc.contributor.institutionLaboratory of Organic & Microwave-Assisted Chemistry (LOMAC), Department of Chemistry, University of Leuven (KU Leuven), Celestijnenlaan 200F, 3001 Leuven, Belgium.en
dc.contributor.institutionPeoples Friendship University of Russia (RUDN University), 6 Miklukho-Maklaya street, Moscow, 117198, Russia.en
kaust.authorPeshkov, Anatoly A.en
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