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chemistry, organic (71) 71
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chemistry, multidisciplinary (24) 24
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Organic Letters, ISSN 1523-7060, 2013, Volume 15, Issue 11, pp. 2818 - 2821
Journal Article
Advanced Synthesis & Catalysis, ISSN 1615-4150, 04/2018, Volume 360, Issue 7, pp. 1370 - 1375
A Co(III)‐catalyzed C−H activation reaction for ortho‐alkenylation of benzamides (aryl/heteroaryl) and C2‐alkenylation of indole derivatives have been... 
alkenylation | amides | C−H activation | Cobalt | alkynyl carboxylic acid | O BOND | ANNULATION | CHEMISTRY, ORGANIC | TERMINAL ALKYNES | COBALT-CATALYZED CYCLIZATION | ISOQUINOLONE SYNTHESIS | ALIPHATIC AMIDES | C-H activation | BENZAMIDES | ARYL | CHEMISTRY, APPLIED | HYDROARYLATION | Amides | Olefins | Organic acids | Alkenes | Regioselectivity | Aromatic compounds | Activation | Carboxylic acids | Substrates | Functional groups
Journal Article
Chemistry – A European Journal, ISSN 0947-6539, 09/2018, Volume 24, Issue 52, pp. 13954 - 13962
Journal Article
Organic Letters, ISSN 1523-7060, 02/2017, Volume 19, Issue 4, pp. 846 - 849
A gold-catalyzed [2,3]-sigmatropic rearrangement reaction has been developed. The intermolecular rearrangement occurs between in situ generated donor–acceptor... 
Journal Article
Advanced Synthesis & Catalysis, ISSN 1615-4150, 09/2018, Volume 360, Issue 18, pp. 3579 - 3584
A Co(III)‐catalyzed counter anion triggered desilylative direct ortho‐vinylation of secondary benzamides is reported. The reaction furnishes the alkenylated... 
alkenylation | alkynylsilane | amides | C−H activation | desilylation | Cobalt | CATALYSIS | O BOND | ANNULATION | ALKYNYL CARBOXYLIC-ACIDS | ARENES | BOND FUNCTIONALIZATION | CHEMISTRY, ORGANIC | ISOQUINOLONE SYNTHESIS | C-H activation | OLEFINATION | CHEMISTRY, APPLIED | HYDROARYLATION | Amides | Anions | Functional groups | Alkynes
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 09/2010, Volume 49, Issue 37, pp. 6622 - 6625
A wide range of primary azides have been efficiently oxidized by a catalytic amount of CuI and TBHP into their corresponding nitriles in aqueous solution. A... 
oxidation | copper | nitriles | azides | tert‐butyl hydroperoxide | Azides | Nitriles | Oxidation | Copper | Tert-butyl hydroperoxide | TRANSFORMATION | tert-butyl hydroperoxide | AQUEOUS-MEDIUM | NUCLEOPHILIC-SUBSTITUTION | MOLYBDENUM XANTHATE | CYANATION | ALDEHYDES | CHEMISTRY, MULTIDISCIPLINARY | DEHYDRATION | PRIMARY AMIDES | HETEROGENEOUS CATALYST | ALDOXIMES
Journal Article
Journal of Organic Chemistry, ISSN 0022-3263, 03/2018, Volume 83, Issue 5, p. 2986
Journal Article
ISSN 1359-7345, 5/2017, Volume 53, Issue 37, pp. 5117 - 512
The C4-aminated indole scaffold is frequently encountered in several natural products and biologically active compounds. Herein we disclose a simple and short... 
Journal Article
Organic Letters, ISSN 1523-7060, 12/2013, Volume 15, Issue 24, pp. 6262 - 6265
A highly regioselective functionalization of indole at the C-4 position by employing an aldehyde functional group as a directing group, and Ru as a catalyst,... 
FUNCTIONALIZATION | PALLADIUM | ACIDS | ARYLATION | ERGOT ALKALOIDS | CHEMISTRY, ORGANIC | BOND FORMATION | ALDEHYDES | IDENTIFICATION | EFFICIENT | ORTHO-ALKENYLATION | Stereoisomerism | Indoles - chemical synthesis | Organometallic Compounds - chemistry | Molecular Structure | Catalysis | Indoles - chemistry | Ruthenium - chemistry
Journal Article
Organic Letters, ISSN 1523-7060, 03/2013, Volume 15, Issue 5, pp. 1092 - 1095
A versatile aerobic catalytic system (I2 and O2/TBHP) for C–H functionalization is reported. This CDC (cross-dehydrogentive coupling) reaction is compatible... 
ACTIVATION | AMINATION | DEHYDROGENATIVE COUPLING REACTIONS | CDC | HETEROCYCLES | TERTIARY-AMINES | CHEMISTRY, ORGANIC | BOND FORMATION | HYDROGEN-PEROXIDE | OXIDATIVE CYANATION | MOLECULAR-OXYGEN
Journal Article
ISSN 1477-0520, 6/2017, Volume 15, Issue 24, pp. 5191 - 5196
An iodine catalyzed sulfenylation of pyrazolones with a diverse range of heterocyclic thiols, heterocyclic thiones and disulfides has been described using... 
Journal Article
The Journal of Organic Chemistry, ISSN 0022-3263, 07/2017, Volume 82, Issue 13, pp. 6913 - 6921
Highly selective azo directed 1,4-addition of an ortho C–H bond to maleimides has been developed using Co­(III) catalyst. This reaction furnishes 3-arylated... 
FUNCTIONALIZATION | ANTICANCER ACTIVITY | MILD CONDITIONS | RING-OPENING REACTIONS | COBALT CATALYSIS | AZOBENZENES | AMIDATION | CHEMISTRY, ORGANIC | INDOLE SYNTHESIS | INTERNAL ALKYNES | RHODIUM CATALYSIS
Journal Article
The Journal of Organic Chemistry, ISSN 0022-3263, 09/2016, Volume 81, Issue 17, pp. 7838 - 7846
A regioselective formation of C–S bonds has been achieved using a cross dehydrogenative coupling (CDC) protocol using iodine as a catalyst and dimethyl... 
KETONES | HETEROARENES | S BOND FORMATION | VINYL SULFONES | THIOLATION | STRATEGY | CHEMISTRY, ORGANIC | INHIBITORS | C-H FUNCTIONALIZATION | EFFICIENT | DERIVATIVES | Chemical bonds | Chemical properties | Research | Catalysis | Heterocyclic aromatic compounds
Journal Article
Organic Letters, ISSN 1523-7060, 06/2013, Volume 15, Issue 11, pp. 2818 - 2821
A highly regioselective alkenylation of indole at the C2-position has been achieved using the Ru(II) catalyst by employing a directing group strategy. This... 
H BOND ACTIVATION | FUNCTIONALIZATION | DIRECT ARYLATION | PROTECTING GROUP | ATOM ECONOMY | CHEMISTRY, ORGANIC | OLEFINS | CARBON-HYDROGEN BONDS | CLEAVAGE | PALLADIUM ACETATE | ORTHO-ALKENYLATION
Journal Article
Advanced Synthesis & Catalysis, ISSN 1615-4150, 01/2020, Volume 362, Issue 1, pp. 152 - 159
A cobalt‐catalyzed regioselective [4+2] annulation/lactonization reaction of benzamides with 4‐hydroxy‐2‐alkynoates is reported. This reaction utilizes air as... 
[4+2] annulation | aerobic condition | lactonization | cobalt | C−H activation | regioselective | ANNULATION | BOND FUNCTIONALIZATION | CHEMISTRY, ORGANIC | ALIPHATIC AMIDES | C-H activation | CARBONYLATION | DIRECTED FUNCTIONALIZATION | AROMATIC AMIDES | BIDENTATE | CHEMISTRY, APPLIED | ACCESS | CYCLIZATION | Organic chemistry | Regioselectivity | Oxidants | Oxidizing agents | Chemical reactions | Substrates | Functional groups
Journal Article
The Journal of Organic Chemistry, ISSN 0022-3263, 03/2017, Volume 82, Issue 6, pp. 3084 - 3093
Synthesis of polyfunctionalized aminothioalkenes has been demonstrated using iodine as a catalyst (30 mol %) and dimethyl sulfoxide as an oxidant under... 
KETONES | HETEROARENES | METAL-FREE CONDITIONS | BROMINATION | S BOND FORMATION | SULFIDES | H FUNCTIONALIZATION STRATEGY | REGIOSELECTIVE SYNTHESIS | CHEMISTRY, ORGANIC | INHIBITORS | DISULFIDES | Chemical properties | Catalysis | Research | Dimethyl sulfoxide | Amino compounds
Journal Article
Advanced Synthesis & Catalysis, ISSN 1615-4150, 11/2019, Volume 361, Issue 21, pp. 4933 - 4940
A manganese‐catalyzed C−H bond alkenylation of indoles at C2‐position with 4‐hydroxy‐2‐alkynoates leading to concomitant lactonization under removable... 
Lactonization | C−H Activation | 4-Hydroxy-2-alkynoate | Indole | Manganese | ACID | C-H Activation | IMINES | ARYLATION | EFFICIENT SYNTHESIS | CHEMISTRY, ORGANIC | BOND FORMATION | ALKYNES | FUNCTIONALIZATION | ESTERS | CHEMISTRY, APPLIED | ACCESS | Indoles | Regioselectivity | Hydrogen bonds | Substrates | Functional groups
Journal Article
The Journal of Organic Chemistry, ISSN 0022-3263, 10/2011, Volume 76, Issue 19, pp. 7938 - 7944
A facile metal-free route of oxidative amination of benzoxazole by activation of C–H bonds with secondary or primary amines in the presence of catalytic iodine... 
AZOLES | FUNCTIONALIZATION | OXIDATION | FORMAMIDES | ACIDS | ARYL HALIDES | ARYLATION | CHEMISTRY, ORGANIC | COPPER | DERIVATIVES | C-H | Iodine - chemistry | Acetates - chemistry | Benzoxazoles - chemistry | Catalysis | Amination | Green Chemistry Technology - methods | Iodine compounds | Oxazoles | Analysis | Amino compounds | Chemical bonds | Chemical properties
Journal Article
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