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Organic Letters, ISSN 1523-7060, 03/2016, Volume 18, Issue 6, pp. 1278 - 1281
A palladium-catalyzed domino reaction via a dehydrogenative aromatization and a dual C­(sp2)–H functionalization process for one-pot synthesis of carbazoles... 
MEDIATED TOTAL-SYNTHESIS | H BOND ACTIVATION | ORGANIC-SYNTHESIS | FUNCTIONALIZED CARBAZOLES | TRANSITION-METAL-COMPLEXES | DOUBLE N-ARYLATION | C-N | DIENE COMPLEXES | 1ST TOTAL-SYNTHESIS | CHEMISTRY, ORGANIC | PRIMARY AMINES
Journal Article
Organic & biomolecular chemistry, ISSN 1477-0520, 06/2016, Volume 14, Issue 21, pp. 4848 - 4852
Synthesis of isoquinolines based on efficient C-C and C-N bond formation through Rh(iii)-catalyzed C-H activation and subsequent intramolecular cyclization is... 
Journal Article
The Journal of Organic Chemistry, ISSN 0022-3263, 06/2017, Volume 82, Issue 12, pp. 6434 - 6440
2′-Aminoacetophenones undergo a C­(sp3)–H oxidation followed by intramolecular C–N bond formation by virtue of a simple electrochemical oxidation in the... 
OXIDATION | ACTIVATION | SUBSTITUTED ISATINS | HALOFORM REACTION | CHEMISTRY, ORGANIC | DOMINO APPROACH | N-ARYLISATINS | ORGANIC ELECTROSYNTHESIS | METHYL KETONES | ELECTROCHEMICAL SYNTHESIS | MOLECULAR-OXYGEN
Journal Article
Organic Letters, ISSN 1523-7060, 05/2013, Volume 15, Issue 9, pp. 2274 - 2277
A metal-free sequential dual oxidative amination of C(sp3)–H bonds under ambient conditions was the first developed, affording imidazo[1,5-a]pyridines in good... 
FUNCTIONALIZATION | INTERMOLECULAR AMINATION | COPPER-CATALYZED AMIDATION | ANILINES | ESTERS | CHEMISTRY, ORGANIC | ALPHA-AMINO-ACIDS | ADJACENT | C-H BONDS | Amination | Hydrogen Bonding | Oxidation-Reduction | Pyridines - chemistry | Imidazoles - chemistry | Pyridines - chemical synthesis | Molecular Structure | Imidazoles - chemical synthesis
Journal Article
Organic Letters, ISSN 1523-7060, 03/2016, Volume 18, Issue 5, pp. 1178 - 1181
A distinct C–H activation-based traceless synthetic protocol via electrophilic removal of a directing group is reported, complementing the currently... 
FUNCTIONALIZATION | FORM ISOCOUMARINS | FACILE SYNTHESIS | MILD CONDITIONS | INTERNAL OXIDANT | EFFICIENT SYNTHESIS | CHEMISTRY, ORGANIC | BOND ACTIVATION | RH(III)-CATALYZED SYNTHESIS | ALKYNES | CARBOXYLIC-ACIDS
Journal Article
Organic Letters, ISSN 1523-7060, 10/2018, Volume 20, Issue 20, pp. 6359 - 6363
An efficient NH4I-mediated intermolecular annulation of methyl N-heteroaromatics with amines/amino acids was developed by virtue of anodic oxidation, providing... 
FUNCTIONALIZATION | ELECTROSYNTHESIS | KETONES | EFFICIENT APPROACH | CHEMISTRY, ORGANIC | TRANSANNULATION | METAL | OXIDATIVE AMINATION | C-H BONDS | CYCLIZATION | ELECTROCHEMICAL SYNTHESIS
Journal Article
Organic and Biomolecular Chemistry, ISSN 1477-0520, 2016, Volume 14, Issue 21, pp. 4848 - 4852
Journal Article
Journal Article
by Fang, WY and Zha, GF and Zhao, C and Qin, HL
CHEMICAL COMMUNICATIONS, ISSN 1359-7345, 06/2019, Volume 55, Issue 44, pp. 6273 - 6276
The construction of para-amino-arylfluorosulfates was achieved through installation of fluorosulfate (-OSO2F) functionality into aromatic C(sp(2))-H bonds by... 
REARRANGEMENT | SULFONYL FLUORIDES | SUFEX CLICK CHEMISTRY | TRANSTHYRETIN | ACIDS | PHENOLS | STRATEGY | ANILINE | ELECTROPHILES | DERIVATIVES | CHEMISTRY, MULTIDISCIPLINARY
Journal Article
Organic Letters, ISSN 1523-7060, 05/2016, Volume 18, Issue 9, pp. 2062 - 2065
An efficient double C–N bond formation sequence to prepare highly substituted quinazolines utilizing benzimidates and dioxazolones under the catalytic... 
DIRECTING GROUP | UNPROTECTED INDOLES | N-N BOND | 2-SUBSTITUTED QUINAZOLINES | ANTIBACTERIAL ACTIVITY | CYCLIZATION REACTIONS | EFFICIENT SYNTHESIS | REGIOSELECTIVE SYNTHESIS | CHEMISTRY, ORGANIC | DEHYDROGENATIVE SYNTHESIS | SUBSTITUTED PYRIDINES
Journal Article
Chemistry – An Asian Journal, ISSN 1861-4728, 03/2013, Volume 8, Issue 3, pp. 534 - 537
Synthesize while the iron is hot: The synthesis of 2‐vinylquinolines via a FeCl3‐catalyzed CH sp3 functionalization and a subsequent CN cleavage is reported.... 
synthesis | 2‐vinylquinolines | iron | radicals | CH functionalization | C-H functionalization | 2-vinylquinolines
Journal Article
The Journal of Physical Chemistry C, ISSN 1932-7447, 02/2017, Volume 121, Issue 7, pp. 3947 - 3957
The self-assembly of 2,7-bis­(decyloxy)-9-fluorenone on highly oriented pyrolytic graphite is investigated at the solid/gas interface by scanning tunneling... 
Journal Article
Organic Letters, ISSN 1523-7060, 07/2017, Volume 19, Issue 13, pp. 3640 - 3643
An efficient Rh­(III)-catalyzed C–H activation protocol has been developed for the synthesis of 2,3-benzodiazepines with use of N-Boc hydrazones and... 
UNPROTECTED INDOLES | INHIBITION | RECEPTOR ANTAGONISTS | HUMAN PLASMA | REDOX-NEUTRAL SYNTHESIS | ONE-POT SYNTHESIS | IN-VIVO | BETA-DIKETONES | CHEMISTRY, ORGANIC | DIAZO-COMPOUNDS | BOND ACTIVATION
Journal Article
Journal of Organic Chemistry, ISSN 0022-3263, 05/2015, Volume 80, Issue 9, pp. 4736 - 4742
A copper-catalyzed radical methylation/sp(3) C-H amination/oxidation reaction for the facile synthesis of quinazolinone was developed. In this cascade... 
C(SP)-H BONDS | METHYL ESTERIFICATION | MEDIATED INTRAMOLECULAR AMINATION | BONDS EFFICIENT SYNTHESIS | ONE-POT SYNTHESIS | INTERMOLECULAR AMIDATION | C-C | CHEMISTRY, ORGANIC | MICROWAVE IRRADIATION | OXIDATIVE AMINATION | BETA-LACTAMS
Journal Article
Journal of Organic Chemistry, ISSN 0022-3263, 03/2019, Volume 84, Issue 6, pp. 3148 - 3157
An NH4I-mediated tandem electrosynthesis of 1,3-disubstituted imidazo[1,5-a]quinolines was developed from readily available starting materials in aqueous... 
MILD | ELECTROSYNTHESIS | EFFICIENT APPROACH | HETEROCYCLES | AMINO-ACIDS | CHEMISTRY, ORGANIC | BOND FORMATION | C-H FUNCTIONALIZATION | OLEFIN COUPLING REACTIONS | CYCLIZATION | ELECTROCHEMICAL SYNTHESIS
Journal Article
Colloid and Polymer Science, ISSN 0303-402X, 05/2016, Volume 294, Issue 5, pp. 841 - 849
Journal Article
Journal of Cellular Biochemistry, ISSN 0730-2312, 08/2017, Volume 118, Issue 8, pp. 2182 - 2192
ABSTRACT Chondrosarcoma, the second‐most frequent primary bone malignancy, is generally more resistant to conventional chemotherapy and radiotherapy.... 
YAP | JQ1 | CHONDROSARCOMA | CELL CYCLE ARREST | p21 | CANCER-CELLS | APOPTOSIS | BIOCHEMISTRY & MOLECULAR BIOLOGY | C-MYC | MECHANISMS | CELL BIOLOGY | LYMPHOMAGENESIS | THERAPY | DEGRADATION | PROGRESSION | BRD4 | Cell Cycle - genetics | Apoptosis - drug effects | Humans | Cell Survival - genetics | Cellular Senescence - drug effects | Apoptosis - genetics | Immunoblotting | Phosphoproteins - metabolism | Cyclin-Dependent Kinase Inhibitor p21 - genetics | Flow Cytometry | RNA Interference | Cyclin-Dependent Kinase Inhibitor p21 - metabolism | Gene Expression Regulation, Neoplastic - drug effects | Gene Expression Regulation, Neoplastic - genetics | Cell Survival - drug effects | Cellular Senescence - genetics | Cell Proliferation - genetics | Signal Transduction - genetics | Phosphoproteins - genetics | Proto-Oncogene Proteins c-myc - metabolism | Azepines - pharmacology | Triazoles - pharmacology | Signal Transduction - drug effects | Chondrosarcoma - metabolism | Adaptor Proteins, Signal Transducing - genetics | Cell Line, Tumor | Cell Proliferation - drug effects | Proto-Oncogene Proteins c-myc - genetics | Adaptor Proteins, Signal Transducing - metabolism | Cell Cycle - drug effects | Proteins - antagonists & inhibitors | Epigenetic inheritance | Chemotherapy | T cells | Tumor proteins | Growth | Cancer | Cell proliferation | Regulations | GTP-binding protein | Chondrosarcoma | Senescence | p53 Protein | c-Myc protein | Lymphocytes T | Malignancy | Bone tumors | Myc protein | Cyclin D1 | Proteins | Cell growth | Bcl-x protein | Lymphocytes | Cell cycle | Inhibition | Radiation therapy | Yes-associated protein | Cyclin-dependent kinase inhibitor p21 | Inhibitors | Cyclin-dependent kinase inhibitor p27 | Bcl protein | In vitro methods and tests | Apoptosis
Journal Article