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Synlett, ISSN 0936-5214, 03/2016, Volume 27, Issue 5, pp. 769 - 772
Abstract An efficient copper-catalyzed C−H/N−H bond functionalization for the synthesis of α-keto- N -acyl sulfoximines from aryl methyl ketones and N... 
letter | ketone | sulfoximine | α-ketoacylation | oxidative coupling | dioxygen
Journal Article
Chemistry – A European Journal, ISSN 0947-6539, 09/2017, Volume 23, Issue 50, pp. 12100 - 12103
An efficient synthesis of N‐propargylsulfoximines was developed through a copper‐catalyzed coupling of aldehydes, alkynes, and NH‐sulfoximines. The reaction... 
multicomponent reactions | aldehyde | copper | alkyne | N-propargylsulfoximine | Copper | Aldehydes | Couplings | Catalysts | Chemical synthesis | Alkynes
Journal Article
Advanced Synthesis & Catalysis, ISSN 1615-4150, 05/2018, Volume 360, Issue 9, pp. 1800 - 1804
Ball milling techniques have been applied in the development of a mechanosynthesis of [Cp*Co(CO)I2], which proved highly efficient as catalyst in... 
mechanosynthesis | cobalt | ball mill | C−H bond functionalization | Amidation | ACTIVATION | ARENES | CHEMISTRY, ORGANIC | NITRENE TRANSFER-REACTIONS | C-H bond functionalization | INDOLES | SOLVENT-FREE | AMIDO TRANSFER | COUPLING REACTIONS | ORGANOMETALLIC SYNTHESIS | C(SP)-H AMINATION | CHEMISTRY, APPLIED | Cobalt | Ball milling | Catalysis | Indoles | Hydrogen bonds | Catalysts
Journal Article
Chemistry – A European Journal, ISSN 0947-6539, 04/2016, Volume 22, Issue 16, pp. 5547 - 5550
Under an atmosphere of dioxygen, copper‐catalyzed de‐alkylation/amination sequences provide sulfonimidamides from unprotected sulfoximines in moderate to good... 
demethylation | copper | sulfoximines | sulfonimidamides | oxygen | ACYL SULFONIMIDAMIDES | ASYMMETRIC-SYNTHESIS | ARYLATION | STEREOCHEMISTRY | SULFUR | CLEAVAGE | CHEMISTRY, MULTIDISCIPLINARY | KETONES | BIOISOSTERES | DERIVATIVES | Copper | Cleavage | Formations | Atmospheres | Bonding | Radicals
Journal Article
Advanced Synthesis & Catalysis, ISSN 1615-4150, 12/2017, Volume 359, Issue 24, pp. 4274 - 4277
A Hofmann‐Löffler‐Freytag type cyclization reaction of S‐aryl‐S‐phenylpropyl sulfoximines (and related derivatives) was developed. Using molecular iodine as... 
Hofmann-Löffler-Freytag reaction | dihydroisothiazole oxides | sulfoximines | Iodine-Mediated | VISIBLE-LIGHT | CATALYSIS | BONDS | CHEMISTRY, ORGANIC | INTRAMOLECULAR FUNCTIONALIZATION | RADICALS | CHEMISTRY, APPLIED | C-H AMINATION | Hofmann-Loffler-Freytag reaction | Oxides | Aromatic compounds | Iodine
Journal Article
Journal of the American Chemical Society, ISSN 0002-7863, 02/2016, Volume 138, Issue 7, pp. 2166 - 2169
Journal Article
Chemistry – A European Journal, ISSN 0947-6539, 10/2017, Volume 23, Issue 56, pp. 13888 - 13892
Journal Article
The Journal of Organic Chemistry, ISSN 0022-3263, 11/2012, Volume 77, Issue 21, pp. 9756 - 9765
A novel iridium-catalyzed asymmetric ring-opening (ARO) reaction of oxabenzonorbornadienes with a variety of phenols was reported, which afforded the... 
BORONIC ACIDS | HETEROBICYCLIC ALKENES | NICKEL-COMPLEXES | AZABICYCLIC ALKENES | OXABICYCLIC ALKENES | N-BOC-AZABENZONORBORNADIENE | CHEMISTRY, ORGANIC | ALLYLIC ALKYLATIONS | GRIGNARD-REAGENTS | AMINE NUCLEOPHILES | ORGANOZINC HALIDES | Thermal properties | Analysis | Crystals | Chemical bonds | Phenols | Catalysis | Iridium | Chemical properties | Structure
Journal Article
Environmental Science & Technology, ISSN 0013-936X, 12/2014, Volume 48, Issue 24, pp. 14490 - 14498
Journal Article
Chemistry : a European journal, ISSN 0947-6539, 09/2017, Volume 23, Issue 50, pp. 12100 - 12103
Journal Article
Organic Letters, ISSN 1523-7060, 11/2017, Volume 19, Issue 21, pp. 6020 - 6023
A Cp*Rh­(III) complex has been used as catalyst for the preparation of unprecedented 1,2-benzothiazepine 1-oxides by [4 + 3] cyclization of NH-sulfoximines... 
ACTIVATION | THIADIAZINE 1-OXIDES | S-ARYL SULFOXIMINES | DRUG DISCOVERY | ALLYLATION | CHEMISTRY | CHEMISTRY, ORGANIC | N BOND FORMATION | OXIDATIVE CYCLIZATION | DERIVATIVES | C-H FUNCTIONALIZATIONS
Journal Article
Organic Letters, ISSN 1523-7060, 12/2017, Volume 19, Issue 23, pp. 6284 - 6287
Under solventless grinding conditions, mechanochemical ruthenium-catalyzed hydroarylations of alkynes with acetanilides lead to trisubstituted alkenes. Only... 
FUNCTIONALIZATION | SOLVENTLESS CONDITIONS | EFFICIENT ROUTE | CHEMISTRY, ORGANIC | STEREOSELECTIVE HYDROARYLATION | BOND ACTIVATION | OXIDATIVE ANNULATION | ANILIDES | C-H ACTIVATION | STRECKER REACTION | INDOLES
Journal Article
Chemistry - A European Journal, ISSN 0947-6539, 10/2017, Volume 23, Issue 56, p. 13888
An N-heterocyclic carbene (NHC)-catalyzed highly diastereo- and enantioselective formal [3+2] reaction of o-hydroxy aromatic aldimines and cinnamaldehydes for... 
Phosphates | Phosphoric acid | Synthesis | Hydrogen | Analysis | Quinone | Crystals | Catalysis | Enantiomers | Structure | Organic compounds | Quinones | Asymmetric synthesis | Hydrogen bonds | Amides | Selectivity | Benzoquinone | Chemical synthesis
Journal Article
中国科学:技术科学英文版, ISSN 1674-7321, 2012, Volume 55, Issue 11, pp. 3200 - 3203
Photoluminescence properties of highly p+-doped GaASl_ySby are investigated. Band gap narrowing (BGN) effect is considered for heavily doped GaAs1_ySby... 
费米能级 | FWHM | 外延层 | 最大值 | 光致发光特性 | p型掺杂 | PL光谱 | 摩尔分数
Journal Article
ACS Catalysis, ISSN 2155-5435, 2015, Volume 5, Issue 5, pp. 2770 - 2773
A ruthenium-catalyzed arylation reaction of oxa- and azabicyclic alkenes with (hetero)­arenes by C–H bond activation has been discovered. The reaction does not... 
C-H bond activation | ruthenium | alkylation | oxygen | oxa- and azabicyclic alkenes | ASYMMETRIC-SYNTHESIS | OXABICYCLIC ALKENES | DIRECT FUNCTIONALIZATION | RING-OPENING REACTIONS | ARENES | CHEMISTRY, PHYSICAL | CARBON-HYDROGEN BONDS | UNACTIVATED ALKENES | H BOND ACTIVATION | C-C | METAL
Journal Article
ChemInform, ISSN 0931-7597, 07/2016, Volume 47, Issue 30, pp. no - no
...ChemInform Abstract The reaction has a broad substrate scope and delivers the products in moderate to high yields. Scheme   Hanchao Cheng , Carsten Bolm... 
ketones (benzene compounds) | catalysis, phase‐transfer catalysis | aldehyde derivatives (acyclic compounds) | sulfoxides, sulfones, sulfenes and derivatives (benzene compounds)
Journal Article
ChemInform, ISSN 0931-7597, 07/2016, Volume 47, Issue 30, p. no
The reaction has a broad substrate scope and delivers the products in moderate to high yields. 
Catalysis | Ketones | Copper | Organosulfur compounds
Journal Article
Environmental Science and Technology, ISSN 0013-936X, 12/2014, Volume 48, Issue 24, pp. 14490 - 14498
Journal Article
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