About: Biomimetic 2-Imino-Nazarov Cyclizations via Eneallene Aziridination

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scientific article published on 10 March 2020

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) article scientifique publié en 2020 (fr) artículu científicu espublizáu en marzu de 2020 (ast) scientific article published on 10 March 2020 (en) 2020 թվականի մարտի 10-ին հրատարակված գիտական հոդված (hy) artykuł naukowy opublikowany 10 marca 2020 (pl) наукова стаття, опублікована 10 березня 2020 (uk)
publication date	wds:Q90108380-6FF3EC22-8554-49F7-B920-68D1234BF8DA
publication date	2020-03-10 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q90108380-201FC1BA-691C-4045-9B94-BF651D485DE8
language of work or name	English
cites work	wds:Q90108380-01743A1C-C600-43EE-9CCF-B95DCA9D594B wds:Q90108380-0801FBD2-A7F2-4F0E-A1D9-2069C35C10FA wds:Q90108380-0C32C059-0FBD-411B-966F-907BCF4F80A2 wds:Q90108380-0E7F33B0-3EA8-4946-9D57-F84A2150F380 wds:Q90108380-19748734-ACAA-4C1D-82E8-03FBABEDADF4 wds:Q90108380-1F2A5C52-0035-4693-89BE-F3AA5A29E5EF wds:Q90108380-2C4E4EA9-6127-4F28-810A-BD5CBE8B214C wds:Q90108380-2D16D00C-6E39-49A3-9D0C-5F5FE6A780EC wds:Q90108380-2E850BF7-E04E-45CD-B9FB-28221D45A408 wds:Q90108380-38F0E869-64AB-4451-9F10-CC8E730FD01C wds:Q90108380-4034342F-C6C6-43AB-8FB8-81D1A895EDA4 wds:Q90108380-54840679-913F-4200-B853-DB503AD7D8B8 wds:Q90108380-56C10C78-0F47-4611-881B-AF144053EB46 wds:Q90108380-57A323AD-74AE-4CA5-9856-6A39BADDCF13 wds:Q90108380-5CBC5FF5-D3AF-4072-A7CD-B78DE31C6074 wds:Q90108380-6125194D-2BA0-4F7E-84E7-4DFFD4776680 wds:Q90108380-6BEB56D5-72D2-4706-B609-8AE793EB393D wds:Q90108380-71178C58-D582-4361-9317-3F616B7312A5 wds:Q90108380-73E9E910-BC0E-48FF-B639-FBA33A8AA705 wds:Q90108380-818F31A3-E2C8-4B29-B2E8-7FF72CCF69BD wds:Q90108380-93926654-A69E-439A-ADF7-A0FD5FE4AD04 wds:Q90108380-9BFA3936-E9D5-4F33-A29E-E8EB502C7C6C wds:Q90108380-BECDF361-BF73-4A55-B880-E27A07D7A28D wds:Q90108380-BEF1A0BC-2738-413F-BA70-DE3859784E7A wds:Q90108380-C49381BA-A5ED-478E-AD85-E38E17AD78AB wds:Q90108380-C77D39A2-A789-4124-94BC-27F2780EE9B8 wds:Q90108380-CDD6D211-51E4-4B87-8EF8-E1C32CBB382F wds:Q90108380-DAB83276-2529-4EBB-94DD-7ACD57839E09 wds:Q90108380-E43DB222-A87F-430B-B51E-F4E7452E44E2 wds:Q90108380-F4E73407-35BD-4428-80E7-1C8202BE5F10 wds:Q90108380-FDE641DA-A839-4FB1-BD24-26C6668BE5A5
cites work	The jasmonate signal pathway Total synthesis of (±)-rocaglamide via oxidation-initiated Nazarov cyclization Enamine-iminium ion Nazarov cyclization of alpha-ketoenones Allene ether Nazarov cyclization Nazarov-like cyclization reactions Direct and stereospecific synthesis of allenes via reduction of propargylic alcohols with Cp2Zr(H)Cl Oxidation-initiated Nazarov cyclization of vinyl alkoxyallenes The retro-Nazarov reaction α-Aryl-substituted allenamides in an imino-Nazarov cyclization cascade catalyzed by Au(I). Rhodium catalyzed allene amination: diastereoselective synthesis of aminocyclopropanes via a 2-amidoallylcation intermediate Theoretical study of the vinyl allene oxide to cyclopent-2-en-1-one rearrangement: mechanism, torquoselectivity and solvent effects Versatile method for the synthesis of 4-aminocyclopentenones: dysprosium(III) triflate catalyzed aza-piancatelli rearrangement Theoretical study of the electrocyclic ring closure of hydroxypentadienyl cations. Catalytic cycloaddition of 2-methyleneaziridines with 1,1-dicyanoalkenes Intermolecular reaction of internal alkynes and imines: propargyl tosylates as key partners in a gold-catalyzed [4 + 1] unusual cyclization leading to cyclopent-2-enimines Rhodium-Catalyzed Alkene Difunctionalization with Nitrenes. Importance of off-cycle species in the acid-catalyzed aza-Piancatelli rearrangement. Structure and reactivity of bicyclic methylene aziridines prepared by intramolecular aziridination of allenes The intramolecular amination of allenes Interrupted imino-Nazarov cyclization of 1-aminopentadienyl cation and related cascade process. Nazarov reactions of vinyl cyclopropylamines: an approach to the imino-Nazarov problem Nazarov reaction: current trends and recent advances in the synthesis of natural compounds and their analogs. Oxidation-Initiated Cyclizations of Pentadienyl Ethers: An Alternative Entry to the Nazarov Reaction. Regioselective Functionalization of Enamides at the α-Carbon via Unsymmetrical 2-Amidoallyl Cations. A Lewis acid catalyzed intramolecular [4+3] cycloaddition route to polycyclic systems that contain a seven-membered ring Stereocontrolled Syntheses of Seven-Membered Carbocycles by Tandem Allene Aziridination/[4+3] Reaction. Lewis Acid-Catalyzed Nucleophilic Addition of Indoles to in Situ-Generated 2-Amidoallyl Cations. A unifying mechanism for the rearrangement of vinyl allene oxide geometric isomers to cyclopentenones. Lewis acid promoted intramolecular (3 + 2) 'cycloadditions' of methyleneaziridines with alkene and alkyne acceptors Catalytic intermolecular alkene oxyamination with nitrenes Versatile One-Pot Synthesis of Polysubstituted Cyclopent-2-enimines from α,β-Unsaturated Amides: Imino-Nazarov Reaction
author name string	wds:Q90108380-B6398C3C-65D4-49C2-8DDE-B16B6113D65B wds:Q90108380-F9A2DFE5-4472-4832-8A7E-79602F269523
author name string	Joshua R Corbin Devin R Ketelboeter
rdfs:label	Biomimetic 2-Imino-Nazarov Cyclizations via Eneallene Aziridination (en) Biomimetic 2-Imino-Nazarov Cyclizations via Eneallene Aziridination (nl)
skos:prefLabel	Biomimetic 2-Imino-Nazarov Cyclizations via Eneallene Aziridination (en) Biomimetic 2-Imino-Nazarov Cyclizations via Eneallene Aziridination (nl)
name	Biomimetic 2-Imino-Nazarov Cyclizations via Eneallene Aziridination (en) Biomimetic 2-Imino-Nazarov Cyclizations via Eneallene Aziridination (nl)
author	wds:Q90108380-4988372E-E1E4-4BBB-AE06-501E4C02D076 wds:Q90108380-7FDF79CB-CDCA-4678-B722-8CA6A493B178
author	Jennifer M Schomaker Israel Fernández
title	wds:Q90108380-2CAE3420-3AB3-4316-B9E0-4967875D196D
title	Biomimetic 2-Imino-Nazarov Cyclizations via Eneallene Aziridination (en)
page(s)	wds:Q90108380-BA6C7237-134A-458C-A83C-D689A6DC04D1
page(s)	5568-5573
instance of	wds:Q90108380-4240832C-1095-484E-BF24-D3EBED148A03
instance of	scholarly article
PubMed ID	wds:Q90108380-3C93D0E4-305B-4580-9C71-D2D2B5182EDD
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/32142272
PubMed ID	32142272
published in	wds:Q90108380-5E373E61-5595-4C7D-A617-C84D2057BFD3
published in	Journal of the American Chemical Society
issue	wds:Q90108380-DCFF0B56-550B-4209-B60B-76DDE68B0EE1

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