About: Regioselective Syntheses of 1,2-Benzothiazines by Rhodium-Catalyzed Annulation Reactions

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scholarly article by Ying Cheng & Carsten Bolm published 14 April 2015 in Angewandte Chemie International Edition

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована у квітні 2015 (uk) im April 2015 veröffentlichter wissenschaftlicher Artikel (de) scholarly article by Ying Cheng & Carsten Bolm published 14 April 2015 in Angewandte Chemie International Edition (en)
publication date	wds:Q57404730-890DF8A2-A9B4-4F8B-9B52-84CCD286D94E
publication date	2015-04-14 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q57404730-556F92CE-C51C-40E1-A1B4-AD2A53452C8F
language of work or name	English
author name string	wds:Q57404730-1659B8C4-0B00-4E68-B4F5-36766CFE07B3
author name string	Ying Cheng
rdfs:label	Regioselective Syntheses of 1,2-Benzothiazines by Rhodium-Catalyzed Annulation Reactions (en) Regioselective Syntheses of 1,2-Benzothiazines by Rhodium-Catalyzed Annulation Reactions (nl)
skos:prefLabel	Regioselective Syntheses of 1,2-Benzothiazines by Rhodium-Catalyzed Annulation Reactions (en) Regioselective Syntheses of 1,2-Benzothiazines by Rhodium-Catalyzed Annulation Reactions (nl)
name	Regioselective Syntheses of 1,2-Benzothiazines by Rhodium-Catalyzed Annulation Reactions (en) Regioselective Syntheses of 1,2-Benzothiazines by Rhodium-Catalyzed Annulation Reactions (nl)
author	wds:Q57404730-40EDC6B5-306D-457B-9025-EEA65C43CFB0
author	Carsten Bolm
title	wds:Q57404730-CC98D51E-995F-413E-870E-CD8B1FD16A4A
title	Regioselective Syntheses of 1,2-Benzothiazines by Rhodium-Catalyzed Annulation Reactions (en)
page(s)	wds:Q57404730-EFA75FB6-BDB4-400B-80BA-AFCA3C3FE05F
page(s)	12349-12352
instance of	wds:Q57404730-16816F4D-3834-41B0-BB29-680AFE76FC05
instance of	scholarly article
main subject	wds:Q57404730-008DB2E2-DA17-45FD-BFF0-6693AFCF452F wds:Q57404730-25724CE5-33B3-400F-8A4F-AA6F9A05AF01 wds:Q57404730-4D0550ED-A359-47CF-A586-F6B5656F1C46
main subject	rhodium general chemistry catalysis
PubMed ID	wds:Q57404730-0A98A5E1-371E-4821-A8C8-532C49C40EEE
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/25873036
PubMed ID	25873036
published in	wds:Q57404730-ECD0B7AF-EA61-493F-B551-83517285618D
published in	Angewandte Chemie International Edition
issue	wds:Q57404730-08E18B3D-DBC2-475F-8F99-CA6B6E684059
volume	wds:Q57404730-889560B2-3A84-415F-88FC-BC319DE59379
issue	42
volume	54
DOI	wds:Q57404730-A1BE2DC8-0D04-4C57-9902-BA1D95303E8E
DOI	http://dx.doi.org/10.1002/ANIE.201501583
DOI	10.1002/ANIE.201501583
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q57404730
is cites work of	Kooperative Lewis-Säure/Cp*CoIII-katalysierte C-H-Bindungsaktivierung zur Synthese von Isochinolin-3-onen Copper-catalyzed N-methylation/ethylation of sulfoximines. Copper-Catalyzed S-C/S-N Bond Interconversions. Transfer of Electrophilic NH Using Convenient Sources of Ammonia: Direct Synthesis of NH Sulfoximines from Sulfoxides Regio-selective synthesis of diversely substituted benzo[a]carbazoles through Rh(iii)-catalyzed annulation of 2-arylindoles with α-diazo carbonyl compounds. Microwave-Assisted Synthesis of Heterocycles by Rhodium(III)-Catalyzed Annulation of N-Methoxyamides with α-Chloroaldehydes. A comprehensive overview of directing groups applied in metal-catalysed C-H functionalisation chemistry Mechanistic investigation of the NH-sulfoximination of sulfide. Evidence for λ6-sulfanenitrile intermediates. IrIII -Catalyzed One-Pot Cascade Synthesis of Pentacyclic-Fused Carbazoles from Indoles and Diazoes. Rhodium-catalyzed C-H activation of 3-(indolin-1-yl)-3-oxopropanenitriles with diazo compounds and tandem cyclization leading to hydrogenated azepino[3,2,1-hi]indoles. Rh(III)-Catalyzed C-H Activation/Intramolecular Cyclization: Access to N-Acyl-2,3-dihydro-1H-carbazol-4(9H)-ones from Cyclic 2-Diazo-1,3-diketones and N-Arylamides Rhodium-catalyzed benzoisothiazole synthesis by tandem annulation reactions of sulfoximines and activated olefins. Benzo[c]isothiazole 2-Oxides: Three-Dimensional Heterocycles with Cross-Coupling and Functionalization Potential Synthesis of isoquinolines via Rh-catalyzed C-H activation/C-N cyclization with diazodiesters or diazoketoesters as a C2 source. Regioselective synthesis of multisubstituted isoquinolones and pyridones via Rh(III)-catalyzed annulation reactions. Microwave-Assisted Synthesis of Heterocycles by Rhodium(III)-Catalyzed Annulation of N -Methoxyamides with α-Chloroaldehydes Rhodium-Catalyzed ortho -Amidations in the Preparation of Thiadiazine 1-Oxides Copper-Catalyzed Regioselective Cascade Alkylation and Cyclocondensation of Quinoline N-Oxides with Diazo Esters: Direct Access to Conjugated π-Systems. A divergent and metal free synthesis of sulfoximine tethered imidazoles, imidazopyridines, imidazothiazoles, imidazobenzothiazines, thiazoles and selenazoles.
is cites work of	wds:Q48376325-35A47FFF-96C4-41E7-B122-56FBA2A32DCC wds:Q49687209-C11221A7-85E1-4A97-B73C-146AAF90C6C8 wds:Q48369161-FF270303-B935-48E0-991D-015F5235F1E6 wds:Q51786580-490BEFD7-5EF0-4E14-8BF5-C4BDB4D955EF wds:Q41531242-1E8DCAEF-C928-4908-B5CC-CA87BDBC0F10 wds:Q57657035-67163468-BE11-4891-BEF5-8812A3C725AD wds:Q51345322-CE7CB800-82D5-4527-A229-FD7D126C759B wds:Q52884208-DF3527C1-1B9C-40ED-B70B-47D8707A23E4 wds:Q57404718-A1DE91DD-AB5D-4BD0-B63A-13AE3A292BC4 wds:Q51098702-2CBC7F91-74BC-4B9D-AB48-1AD687052250 wds:Q48300356-20A88AE8-4928-49E8-A7DA-0DB0BA473791 wds:Q50730291-E90271FD-7EBA-457C-930F-6000F4DB837D wds:Q54451997-30A3D730-7097-4692-831F-E92B251EA5D3 wds:Q57404720-6D900BF7-3EA4-4AE3-8D27-D31BAA3C6BE9 wds:Q92926908-B97AEAED-9DC9-4F07-8D93-E75B1796C115 wds:Q57404696-750589D0-A421-4ED3-8180-18166CAAF96E wds:Q48958818-81E076A2-DCC4-4A31-8D4E-23124D3BEFE4 wds:Q51687706-101FC934-618C-4EB8-9710-35F6061A8C04 wds:Q58420199-D80EF115-5E4E-43F1-8B16-5B29D36AA20F

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