| scholarly article | Q13442814 |
| P356 | DOI | 10.1039/C7CC01717K |
| P698 | PubMed publication ID | 28367542 |
| P50 | author | Keiji Mori | Q59555298 |
| P2093 | author name string | Taira Yoshida | |
| P2860 | cites work | Palladium-Catalyzed Ligand-Directed C−H Functionalization Reactions | Q29012891 |
| Catalytic C–H functionalization by metal carbenoid and nitrenoid insertion | Q29308505 | ||
| Innate and Guided C–H Functionalization Logic | Q30054500 | ||
| Formation of N-alkylpyrroles via intermolecular redox amination | Q33885988 | ||
| C-H bond functionalization via hydride transfer: Lewis acid catalyzed alkylation reactions by direct intramolecular coupling of sp3 C-H bonds and reactive alkenyl oxocarbenium intermediates | Q34198744 | ||
| C-H bond functionalization via hydride transfer: synthesis of dihydrobenzopyrans from ortho-vinylaryl akyl ethers | Q34198769 | ||
| Asymmetric Redox-Annulation of Cyclic Amines | Q36142441 | ||
| Aryl-aryl bond formation by transition-metal-catalyzed direct arylation. | Q36702962 | ||
| Metal-free α-amination of secondary amines: computational and experimental evidence for azaquinone methide and azomethine ylide intermediates | Q36844734 | ||
| Redox-neutral copper(II) carboxylate catalyzed α-alkynylation of amines | Q37173876 | ||
| Palladium(II)-catalyzed C-H activation/C-C cross-coupling reactions: versatility and practicality | Q37294999 | ||
| Organocatalytic C-H activation reactions. | Q38047283 | ||
| Structure-activity studies for a novel series of tricyclic substituted hexahydrobenz[e]isoindole alpha(1A) adrenoceptor antagonists as potential agents for the symptomatic treatment of benign prostatic hyperplasia (BPH). | Q40884000 | ||
| Redox-neutral α-C-H bond functionalization of secondary amines with concurrent C-P bond formation/N-alkylation | Q41862545 | ||
| Tunable hydride transfer in the redox amination of indoline with aldehyde: an attractive intramolecular hydrogen-bond effect. | Q42835855 | ||
| Enantioselective organocatalytic C-H bond functionalization via tandem 1,5-hydride transfer/ring closure: asymmetric synthesis of tetrahydroquinolines | Q42940768 | ||
| Expeditious synthesis of benzopyrans via Lewis acid-catalyzed C-H functionalization: remarkable enhancement of reactivity by an ortho substituent | Q43123804 | ||
| Thermal cyclization of phenylallenes that contain ortho-1,3-dioxolan-2-yl groups: new cascade reactions initiated by 1,5-hydride shifts of acetalic H atoms. | Q43523759 | ||
| Synthesis of (-)-PNU-286607 by asymmetric cyclization of alkylidene barbiturates | Q44556801 | ||
| Scope of palladium-catalyzed alkylative ring opening | Q44753462 | ||
| Rh-catalyzed isomerization and intramolecular redox reaction of alkynyl ethers affording dihydropyrans and ketoolefins | Q46125338 | ||
| Reagent-controlled regiodivergent resolution of unsymmetrical oxabicyclic alkenes using a cationic rhodium catalyst. | Q46165067 | ||
| Catalytic enantioselective tert-aminocyclization by asymmetric binary acid catalysis (ABC): stereospecific 1,5-hydrogen transfer. | Q50508847 | ||
| Enantioselective gold-catalyzed functionalization of unreactive sp3 C-H bonds through a redox-neutral domino reaction. | Q50526544 | ||
| Highly enantioselective synthesis of tetrahydroquinolines via cobalt(II)-catalyzed tandem 1,5-hydride transfer/cyclization. | Q50528956 | ||
| Product-selectivity control by the nature of the catalyst: Lewis acid-catalyzed selective formation of ring-fused tetrahydroquinolines and tetrahydroazepines via intramolecular redox reaction. | Q50544252 | ||
| The redox-neutral approach to C-H functionalization. | Q51785550 | ||
| Organometallic chemistry: C-H activation. | Q53199987 | ||
| High Facial Diastereoselectivity in Intra- and Intermolecular Reactions of Chiral Benzylic Cations | Q56028492 | ||
| Chiral α-Branched Benzylic Carbocations: Diastereoselective Intermolecular Reactions with Arene Nucleophiles and NMR Spectroscopic Studies | Q57072612 | ||
| Organocatalytic Asymmetric Direct C sp 3H Functionalization of Ethers: A Highly Efficient Approach to Chiral Spiroethers | Q58374761 | ||
| Zinc(II)-Catalyzed Redox Cross-Dehydrogenative Coupling of Propargylic Amines and Terminal Alkynes for Synthesis of N-Tethered 1,6-Enynes | Q58615253 | ||
| P433 | issue | 31 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | diastereoselectivity | Q64131393 |
| P304 | page(s) | 4319-4322 | |
| P577 | publication date | 2017-04-03 | |
| P1433 | published in | Chemical Communications | Q426303 |
| P1476 | title | Hf(OTf)4-Catalyzed highly diastereoselective synthesis of 1,3-disubstituted tetralin derivatives via benzylic C(sp3)-H bond functionalization. | |
| P478 | volume | 53 |
| Q64916014 | Highly diastereoselective synthesis of tricyclic fused-pyrans by sequential hydride shift mediated double C(sp3)-H bond functionalization. |
| Q55054476 | Intramolecular hydride transfer onto arynes: redox-neutral and transition metal-free C(sp3)-H functionalization of amines. |
| Q90442481 | Redox-triggered cascade dearomative cyclizations enabled by hexafluoroisopropanol |
Search more.