About: Catalytic Enantioselective Amination of Silyl Enol Ethers Using Chiral Dirhodium(II) Carboxylates: Asymmetric Formal Synthesis of (−)-Metazocine†

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About: Catalytic Enantioselective Amination of Silyl Enol Ethers Using Chiral Dirhodium(II) Carboxylates: Asymmetric Formal Synthesis of (−)-Metazocine† Goto Sponge NotDistinct Permalink

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scientific article published on 26 September 2007

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в жовтні 2007 (uk) im Oktober 2007 veröffentlichter wissenschaftlicher Artikel (de) scientific article published on 26 September 2007 (en) artículu científicu espublizáu en setiembre de 2007 (ast)
publication date	wds:Q58221138-B54F92F5-6CE1-4CB3-9638-4E686943A8C3
publication date	2007-09-26 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q58221138-4556FCFC-265E-4014-8705-4A0648641D8F
language of work or name	English
author name string	wds:Q58221138-6C916CEA-9F43-4C48-882B-3CD011A84ADE wds:Q58221138-77A4C626-18EB-4260-BAE7-97DD492C6802 wds:Q58221138-E3630D73-8203-492C-BBE5-5D8DCDE30BF4 wds:Q58221138-F1DC8DD3-D3DA-4CCB-B2C9-BF026019DF6B
author name string	Masahiko Tanaka Shunichi Hashimoto Minoru Yamawaki Takuya Washio
rdfs:label	Catalytic Enantioselective Amination of Silyl Enol Ethers Using Chiral Dirhodium(II) Carboxylates: Asymmetric Formal Synthesis of (−)-Metazocine† (en) Catalytic Enantioselective Amination of Silyl Enol Ethers Using Chiral Dirhodium (nl)
skos:prefLabel	Catalytic Enantioselective Amination of Silyl Enol Ethers Using Chiral Dirhodium(II) Carboxylates: Asymmetric Formal Synthesis of (−)-Metazocine† (en) Catalytic Enantioselective Amination of Silyl Enol Ethers Using Chiral Dirhodium (nl)
name	Catalytic Enantioselective Amination of Silyl Enol Ethers Using Chiral Dirhodium(II) Carboxylates: Asymmetric Formal Synthesis of (−)-Metazocine† (en) Catalytic Enantioselective Amination of Silyl Enol Ethers Using Chiral Dirhodium (nl)
author	wds:Q58221138-0C0E4025-CA90-43BC-9EF4-BFBF0922D546 wds:Q58221138-E35D20DC-4470-4B9B-9A99-29044FFA6B05
author	Takumi Abe Masahiro Anada
title	wds:Q58221138-7D6F5E45-E9EB-4ED4-8EA1-C21EDD6735CC
title	Catalytic enantioselective amination of silyl enol ethers using chiral dirhodium(II) carboxylates: asymmetric formal synthesis of (-)-metazocine (en)
page(s)	wds:Q58221138-92110219-226D-496E-B8C0-23E4E5A8CE99
page(s)	4559-4562
instance of	wds:Q58221138-D84514BA-B369-4F6F-B38C-48B321C5C881
instance of	scholarly article
main subject	wds:Q58221138-4BE97EBA-E5EE-4079-8DE7-7A603E90CF37 wds:Q58221138-98BB9C69-367A-4FF9-B1F0-88D71B305405
main subject	chirality enantioselectivity
PubMed ID	wds:Q58221138-8824B106-3F33-4298-ACFE-C0C581BA766C
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/17894504
PubMed ID	17894504
published in	wds:Q58221138-D3DFCFE6-3613-4E47-8B1E-0FB2EC99CB4B
published in	Organic Letters
issue	wds:Q58221138-B8D97217-3F01-4E74-AE06-E94F8D5926B8
volume	wds:Q58221138-7DD8C63D-4821-479E-8712-187E2EA7D212
issue	22
volume	9
number of pages	wds:Q58221138-B1B0AFBB-2174-4D3C-BD86-A3712285184A
number of pages	4 (xsd:decimal)
DOI	wds:Q58221138-FDCCE51E-70CF-4E0F-850B-36EF48F49A07
DOI	http://dx.doi.org/10.1021/OL702019B
DOI	10.1021/OL702019B
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q58221138
is cites work of	Hypervalent iodine reagents in the total synthesis of natural products Rh(2)(S-PTTL)(3)TPA-A Mixed Ligand Dirhodium(II) Catalyst for Enantioselective Reactions of α-Alkyl-α-Diazoesters Chiral crown conformation of Rh(2)(S-PTTL)(4): enantioselective cyclopropanation with alpha-alkyl-alpha-diazoesters Chemistry of polyvalent iodine Allylic C-H amination for the preparation of syn-1,3-amino alcohol motifs Transition-metal-catalyzed aminations and aziridinations of C-H and C=C bonds with iminoiodinanes A Nucleophilic Strategy for Enantioselective Intermolecular α-Amination: Access to Enantioenriched α-Arylamino Ketones Catalytic asymmetric transannulation of NH-1,2,3-triazoles with olefins Asymmetric nitrene transfer reactions: sulfimidation, aziridination and C-H amination using azide compounds as nitrene precursors. Transition metal-catalyzed iodine(iii)-mediated nitrene transfer reactions: efficient tools for challenging syntheses. A Rh(II)-catalyzed multicomponent reaction by trapping an α-amino enol intermediate in a traditional two-component reaction pathway. Catalytic Enantioselective Functionalization of Unactivated Terminal Alkenes Synthesis of 1,4-amino alcohols by Grignard reagent addition to THF and N-tosyliminobenzyliodinane. Making expensive dirhodium(II) catalysts cheaper: Rh(II) recycling methods. Copper(II) triflate catalyzed amination of 1,3-dicarbonyl compounds. Base-catalyzed N-N bond cleavage of hydrazones: synthesis of α-amino ketones.
is cites work of	wds:Q46943397-AFE1E14B-A021-4113-91AD-1F3C912BA047 wds:Q37019352-214B46FA-A00F-4CA1-B4B7-F21619EEDE03 wds:Q33849191-FAB17707-922C-4BF0-A61E-A287E6BB2BE7 wds:Q37994587-5CA65E27-A551-41B0-BC26-74FD44CAD9CC wds:Q42547866-CFA2EB99-DE83-44C7-9B58-6D5A6D904AF6 wds:Q37495203-D1FFD3B8-8AA9-4B5F-A4EE-DCAB3AFAF78F wds:Q41981595-F3C14CF5-C22F-440B-9E57-4F0E79CD56FE wds:Q51333657-CA3AA6BC-3D53-475C-99B2-E26177F06EC2 wds:Q37688738-4D8F0182-6E12-4E19-BE71-45F95A9F26B2 wds:Q37914735-908F3C86-9890-4AF4-8D97-A265787E392B wds:Q37961656-C4F2B39A-0DC2-4EAD-AED7-1D31344B0DBE wds:Q37318116-6274D41A-808E-437A-BC90-97BB91DAE3C5 wds:Q41558254-7DB887DB-7057-4A2C-9A56-5AEA0756B8D3 wds:Q53063840-448143C1-CF06-4D62-8ED8-7272173435CB wds:Q48184302-3F5F9DED-E7C3-4257-9D82-447785F5AAAA wds:Q50762966-D1E24AF7-DF60-4309-BEC0-6C0DC4EEC130

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