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Journal Article
The Journal of Organic Chemistry, ISSN 0022-3263, 04/2013, Volume 78, Issue 8, pp. 3636 - 3646
Journal Article
Journal Article
The Journal of Organic Chemistry, ISSN 0022-3263, 06/2013, Volume 78, Issue 11, pp. 5700 - 5704
Journal Article
Journal of Medicinal Chemistry, ISSN 0022-2623, 11/2012, Volume 55, Issue 21, pp. 9089 - 9106
Journal Article
Inorganic Chemistry, ISSN 0020-1669, 05/2016, Volume 55, Issue 10, pp. 4850 - 4863
Journal Article
Organic Letters, ISSN 1523-7060, 05/2010, Volume 12, Issue 10, pp. 2234 - 2237
Journal Article
Organic Letters, ISSN 1523-7060, 07/2011, Volume 13, Issue 13, pp. 3542 - 3545
2H-Indazoles are synthesized using copper-catalyzed, one-pot, three-component reactions of 2-bromobenzaldehydes, primary amines, and sodium azide. A copper... 
CUPRIC ACETATE | HALIDES | AMINATION | DESIGN | COUPLING REACTIONS | INDAZOLES | CHEMISTRY, ORGANIC | ARYL AZIDES | INHIBITORS | TAUTOMERISM | DERIVATIVES | Molecular Structure | Copper - chemistry | Catalysis | Nitrogen - chemistry | Indazoles - chemical synthesis | Carbon - chemistry
Journal Article
Organic Letters, ISSN 1523-7060, 10/2010, Volume 12, Issue 20, pp. 4576 - 4579
A variety of N-aryl-1H-indazoles and benzimidazoles were synthesized from common arylamino oximes in good to excellent yields. The product selectivity depends... 
1-ARYL-1H-INDAZOLES | PYRAZOLES | EFFICIENT SYNTHESIS | INDAZOLES | CHEMISTRY, ORGANIC | DERIVATIVES | CYCLIZATION | Molecular Structure | Ethylamines - chemistry | Indazoles - chemical synthesis | Benzimidazoles - chemical synthesis
Journal Article
Organic Letters, ISSN 1523-7060, 07/2011, Volume 13, Issue 13, pp. 3340 - 3343
Readily available, stable, and inexpensive N-tosylhydrazones react with arynes under mild reaction conditions to afford 3-substituted indazoles in moderate to... 
GENERATED IN-SITU | 1,3-DIPOLAR CYCLOADDITION | CHEMISTRY, ORGANIC | BAMFORD-STEVENS REACTION | DIAZO-COMPOUNDS | 1H-INDAZOLES | DERIVATIVES | SELECTIVITY | SALTS | Molecular Structure | Indazoles - chemical synthesis | Stereoisomerism | Hydrazones - chemistry
Journal Article
Journal Article
European Journal of Organic Chemistry, ISSN 1434-193X, 12/2017, Volume 2017, Issue 45, pp. 6604 - 6608
A facile, one‐pot synthesis of 1H‐indazoles featuring a Cu‐catalyzed C–H ortho‐hydroxylation and N–N bond‐formation sequence with the use of pure oxygen as the... 
Domino reactions | C–H activation | Hydroxylation | Nitrogen heterocycles | Copper | ACTIVATION | ONE-POT SYNTHESIS | AMIDATION | CHEMISTRY, ORGANIC | 1H-INDAZOLES | BENZYDAMINE | FUNCTIONALIZATION | CROSS-COUPLING REACTIONS | C-H activation | INDAZOLE | DERIVATIVES | CYCLIZATION
Journal Article
The Journal of Organic Chemistry, ISSN 0022-3263, 02/2018, Volume 83, Issue 3, pp. 1591 - 1597
3-Alkyl/aryl-1H-indazoles and 3-alkyl/aryl-3H-indazole-3-phosphonates were synthesized efficiently through a 1,3-dipolar cycloaddition reaction between... 
ASYMMETRIC MANNICH REACTION | 1,3-DIPOLAR CYCLOADDITIONS | PHOSPHONATES | DIELS-ALDER REACTIONS | REGIOSELECTIVE SYNTHESIS | INDAZOLES | CHEMISTRY, ORGANIC | DIAZO-COMPOUNDS | ALPHA-DIAZOMETHYLPHOSPHONATES | ARYNES | BOND | Usage | Chemical properties | Ring formation (Chemistry) | Chemical synthesis | Methyl groups
Journal Article
Journal of Medicinal Chemistry, ISSN 0022-2623, 04/2012, Volume 55, Issue 7, pp. 3364 - 3386
Journal Article
Journal Article
Journal of Medicinal Chemistry, ISSN 0022-2623, 06/2012, Volume 55, Issue 11, pp. 5188 - 5219
A highly selective series of inhibitors of the class I phosphatidylinositol 3-kinases (PI3Ks) has been designed and synthesized. Starting from the dual... 
MAMMALIAN TARGET | RAPAMYCIN | CROSS-COUPLING REACTIONS | CHEMISTRY, MEDICINAL | PI3K | C-N | PATHWAY | KINASE INHIBITOR | MUTATIONS | CANCER | DISCOVERY | Indazoles - chemical synthesis | Pyrazoles - chemical synthesis | Pyrimidines - chemical synthesis | Humans | Microsomes, Liver - metabolism | Pyridines - pharmacokinetics | Biological Availability | Crystallography, X-Ray | Structure-Activity Relationship | Sulfones - pharmacology | TOR Serine-Threonine Kinases - antagonists & inhibitors | Drug Design | Female | Piperazines - pharmacokinetics | Pyrazoles - pharmacokinetics | Pyrazoles - pharmacology | Sulfones - chemical synthesis | Purines - chemical synthesis | Triazines - pharmacology | Signal Transduction | Purines - pharmacology | Purines - pharmacokinetics | Pyridines - chemical synthesis | Models, Molecular | Rats | Proto-Oncogene Proteins c-akt - physiology | Pyrimidines - pharmacology | Sulfones - pharmacokinetics | Sulfonamides - pharmacology | Class I Phosphatidylinositol 3-Kinases - antagonists & inhibitors | Piperazines - pharmacology | Sulfonamides - pharmacokinetics | Indazoles - pharmacology | Xenograft Model Antitumor Assays | Sulfonamides - chemical synthesis | Animals | Class I Phosphatidylinositol 3-Kinases - physiology | Indazoles - pharmacokinetics | Mice, Nude | Triazines - chemical synthesis | Pyrimidines - pharmacokinetics | Piperazines - chemical synthesis | Mice | Pyridines - pharmacology | Triazines - pharmacokinetics | DESIGN | NEOPLASMS | BASIC BIOLOGICAL SCIENCES | PHOSPHOTRANSFERASES | IN VIVO | PROTEINS | 60 APPLIED LIFE SCIENCES
Journal Article
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