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1. Full Text Rh‐Catalyzed Aminative Dearomatization of Naphthols with Hydroxylamine‐O‐Sulfonic Acid (HOSA)
by Yi, Ji‐Cheng and Wu, Zhi‐Jie and You, Shu‐Li
European Journal of Organic Chemistry, ISSN 1434-193X, 09/2019, Volume 2019, Issue 33, pp. 5736 - 5739
An efficient Rh‐catalyzed aminative dearomatization of naphthols was achieved. In the presence of Rh2(esp)2 and HOSA as an inexpensive and readily available... 
Dearomatization | Naphthol | Amination | Rhodium | Homogeneous catalysis | ENANTIOSELECTIVE DEAROMATIZATION | BETA-NAPHTHOLS | ASYMMETRIC DEAROMATIZATION | ARYLATIVE DEAROMATIZATION | OXIDATIVE DEAROMATIZATION | CHEMISTRY, ORGANIC | BOND FORMATION | INTRAMOLECULAR DEAROMATIZATION | SPIROLACTONIZATION | 2-NAPHTHOLS | PHENOL DEAROMATIZATION | Hydroxides
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2. Full Text Rh-Catalyzed aminative dearomatization of 2-naphthols
by Yi, Ji-Cheng and Yi, Ji-Cheng and Tu, Hang-Fei and You, Shu-Li and You, Shu-Li
Organic and Biomolecular Chemistry, ISSN 1477-0520, 2018, Volume 16, Issue 45, pp. 8700 - 8703
A direct aminative dearomatization of 2-naphthols was achieved. In the presence of 1 mol% Rh-2(esp)(2) and 3 equivalents of O-(2,4-dinitrophenyl)hydroxylamine... 
BETA-NAPHTHOLS | ENANTIOSELECTIVE DEAROMATIZATION | ASYMMETRIC DEAROMATIZATION | ARYLATIVE DEAROMATIZATION | OXIDATIVE DEAROMATIZATION | CHEMISTRY, ORGANIC | BOND FORMATION | PHENOL DEAROMATIZATION | INTRAMOLECULAR DEAROMATIZATION | 3+2 SPIROANNULATION | SPIROLACTONIZATION
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3. Full Text Direct halogenative dearomatization of 2-naphthols by NXS (X = Cl, Br) in water
by Zhang, Zhenbei and Sun, Qiangsheng and Xu, Daqian and Xia, Chungu and Sun, Wei
Green Chemistry, ISSN 1463-9262, 2016, Volume 18, Issue 20, pp. 5485 - 5492
A direct halogenative dearomatization of substituted 2-naphthols was achieved by NXS (X = Cl, Br) in environmentally friendly water at room temperature. The... 
ASYMMETRIC DEAROMATIZATION | GREEN & SUSTAINABLE SCIENCE & TECHNOLOGY | HYDROXYLATIVE PHENOL DEAROMATIZATION | ENANTIOSELECTIVE SYNTHESIS | OXIDATIVE DEAROMATIZATION | ONE-POT SYNTHESIS | N-BROMOSUCCINIMIDE | AQUEOUS-MEDIA | BETA-KETO-ESTERS | INTRAMOLECULAR DEAROMATIZATION | CHEMISTRY, MULTIDISCIPLINARY | NAPHTHOL DEAROMATIZATION | Substrates
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4. Full Text Catalytic asymmetric dearomatization (CADA) reactions of phenol and aniline derivatives
by Wu, Wen-Ting and Zhang, Liming and You, Shu-Li
Chemical Society reviews, ISSN 0306-0012, 03/2016, Volume 45, Issue 6, pp. 1570 - 1580
Phenols are widely used as starting materials in both industrial and academic society. Dearomatization reactions of phenols provide an efficient way to... 
Aniline Compounds - chemistry | Catalysis | Oxidation-Reduction | Phenol - chemistry
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5. Full Text Iridium‐Catalyzed Intermolecular Asymmetric Dearomatization of β‐Naphthols with Allyl Alcohols or Allyl Ethers
by Tu, Hang‐Fei and Zheng, Chao and Xu, Ren‐Qi and Liu, Xi‐Jia and You, Shu‐Li
Angewandte Chemie International Edition, ISSN 1433-7851, 03/2017, Volume 56, Issue 12, pp. 3237 - 3241
An Ir‐catalyzed intermolecular asymmetric dearomatization reaction of β‐naphthols with allyl alcohols or allyl ethers was developed. When an iridium catalyst... 
iridium | naphthol | allylic substitution | asymmetric catalysis | dearomatization | ARYLATIVE DEAROMATIZATION | OXIDATIVE DEAROMATIZATION | SUBSTITUTION-REACTIONS | INTRAMOLECULAR DEAROMATIZATION | CHEMISTRY, MULTIDISCIPLINARY | LEAVING GROUPS | KINETIC RESOLUTION | C-C | ALPHA-ALLYLATION | PHENOL DEAROMATIZATION | GRIGNARD-REAGENTS
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6. Full Text Modular Assembly of Spirocarbocyclic Scaffolds through Pd-0-Catalyzed Intermolecular Dearomatizing [2+2+1] Annulation of Bromonaphthols with Aryl Iodides and Alkynes
by Zuo, ZJ and Wang, H and Fan, LX and Liu, JJ and Wang, YY and Luan, XJ
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, ISSN 1433-7851, 03/2017, Volume 56, Issue 10, pp. 2767 - 2771
A novel palladium(0)-catalyzed dearomatizing [2+2+1] spiroannulation of 1-bromo-2-naphthols with aryl iodides and alkynes was developed for the rapid assembly... 
NAPHTHOLS | OXIDATIVE DEAROMATIZATION | CATALYZED SYNTHESIS | ALKYLATION | dearomatization | spiroannulation | INTRAMOLECULAR DEAROMATIZATION | CHEMISTRY, MULTIDISCIPLINARY | INDOLES | SEQUENTIAL REACTIONS | ASYMMETRIC ALLYLIC DEAROMATIZATION | C-H activation | homogeneous catalysis | CONSTRUCTION | palladium | SPIRO
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7. Full Text Pd(0)-Catalyzed intramolecular arylative dearomatization of β-naphthols
by Xu, Ren-Qi and Yang, Ping and You, Shu-Li
Chemical communications (Cambridge, England), ISSN 1359-7345, 07/2017, Volume 53, Issue 54, pp. 7553 - 7556
An efficient Pd(0)-catalyzed intramolecular arylative dearomatization of β-naphthols is described. Using Q-Phos as a ligand, the arylative dearomatization... 
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8. Full Text Gold‐Catalyzed Dearomatization of 2‐Naphthols with Alkynes
by An, Juzeng and Parodi, Adriano and Monari, Magda and Reis, Marta Castiñeira and Lopez, Carlos Silva and Bandini, Marco
Chemistry – A European Journal, ISSN 0947-6539, 12/2017, Volume 23, Issue 69, pp. 17473 - 17477
The site‐selective dearomatization of naphthols is realized in a straightforward manner through a gold(I)‐catalyzed [3,3]‐sigmatropic rearrangement/allene... 
gold | naphthol | catalysis | mechanism | dearomatization | BETA-NAPHTHOLS | MICHAEL REACTION | PROPARGYL CLAISEN REARRANGEMENT | ASYMMETRIC DEAROMATIZATION | OXIDATIVE DEAROMATIZATION | NONCOVALENT INTERACTIONS | INTRAMOLECULAR DEAROMATIZATION | CHEMISTRY, MULTIDISCIPLINARY | INDOLES | CASCADE REACTION | INTERMOLECULAR ARYLATIVE DEAROMATIZATION | Catalysis | Reaction time | Gold | Allene | Ethers | Machinery | Alkynes
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9. Full Text Direct halogenative dearomatization of 2-naphthols by NXS (X = Cl, Br) in water
by Zhang, Zhenbei and Sun, Qiangsheng and Xu, Daqian and Xia, Chungu and Sun, Wei
Green Chemistry, ISSN 1463-9262, 2016, Volume 18, Issue 20, pp. 5485 - 5492
A direct halogenative dearomatization of substituted 2-naphthols was achieved by NXS (X = Cl, Br) in environmentally friendly water at room temperature. The... 
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10. Full Text Catalytic Asymmetric Chlorinative Dearomatization Reaction of Benzofurans
by Liang, Xiao‐Wei and Zheng, Chao and You, Shu‐Li
Advanced Synthesis & Catalysis, ISSN 1615-4150, 06/2016, Volume 358, Issue 13, pp. 2066 - 2071
A catalytic asymmetric chlorinative dearomatization reaction of benzofuran derivatives was achieved by using hydroquinidine 1,4‐phthalazinediyl diether... 
catalytic asymmetric dearomatization (CADA) reaction | organocatalysts | CADA | halofunctionalization | spiro compounds | benzofurans | ANION PHASE-TRANSFER | ARYLATIVE DEAROMATIZATION | ENANTIOSELECTIVE SYNTHESIS | OXIDATIVE DEAROMATIZATION | C BOND FORMATION | EFFICIENT SYNTHESIS | CHEMISTRY, ORGANIC | REISSERT-TYPE REACTION | QUATERNARY STEREOCENTER | ALLYLIC DEAROMATIZATION | PHENOL DEAROMATIZATION | CHEMISTRY, APPLIED | Chlorination | Synthesis | Asymmetry | Catalysts | Reagents | Derivatives | Catalysis | Bearing
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11. Full Text Catalytic asymmetric dearomatization (CADA) reactions of phenol and aniline derivatives
by Wu, Wen-Ting and Zhang, Liming and You, Shu-Li
Chemical Society Reviews, ISSN 0306-0012, 3/2016, Volume 45, Issue 6, pp. 157 - 158
Phenols are widely used as starting materials in both industrial and academic society. Dearomatization reactions of phenols provide an efficient way to... 
ENANTIOSELECTIVE DEAROMATIZATION | BETA-NAPHTHOLS | OXIDATIVE DEAROMATIZATION | C BOND FORMATION | CONSTRUCTION | 2-NAPHTHOLS | ALLYLIC DEAROMATIZATION | 1-AMINONAPHTHALENE DERIVATIVES | CHEMISTRY, MULTIDISCIPLINARY | SPIROLACTONIZATION | CYCLIZATION | Phenol | Asymmetry | Catalysts | Aromaticity | Aniline | Derivatives | Catalysis | Construction industry
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12. Full Text A DFT Study on Rh-Catalyzed Asymmetric Dearomatization of 2‑Naphthols Initiated with C–H Activation: A Refined Reaction Mechanism and Origins of Multiple Selectivity
by Zheng, Chao and Zheng, Jun and You, Shu-Li
ACS Catalysis, ISSN 2155-5435, 01/2016, Volume 6, Issue 1, pp. 262 - 271
Comprehensive DFT calculations have been performed to pursue deeper understandings on the mechanism of Rh-catalyzed asymmetric dearomatization of 2-naphthols... 
enantioselectivity | DFT calculation | asymmetric dearomatization | Rh-catalysis | C-H activation | reaction mechanism | ENANTIOSELECTIVE DEAROMATIZATION | RHODIUM | OXIDATIVE DEAROMATIZATION | CHEMISTRY, PHYSICAL | BOND FORMATION | N BOND | CHIRAL CYCLOPENTADIENYL LIGANDS | COMPUTATIONAL INVESTIGATIONS | ALLYLIC DEAROMATIZATION | PHENOL DEAROMATIZATION | DENSITY-FUNCTIONAL THEORY
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13. Full Text Chiral N,N '-dioxide/Sc(OTf)(3) complex-catalyzed asymmetric dearomatization of beta-naphthols
by Ge, SL and Kang, TF and Lin, LL and Zhang, XY and Zhao, P and Liu, XH and Feng, XM
CHEMICAL COMMUNICATIONS, ISSN 1359-7345, 11/2017, Volume 53, Issue 86, pp. 11759 - 11762
An efficient N,N'-dioxide-scandium(III) complex catalytic system has been developed for the asymmetric dearomatization of beta-naphthols through conjugate... 
ENANTIOSELECTIVE DEAROMATIZATION | HYDROXYLATIVE PHENOL DEAROMATIZATION | ARYLATIVE DEAROMATIZATION | OXIDATIVE DEAROMATIZATION | N,N'-DIOXIDE-SCANDIUM(III) COMPLEXES | ELECTRON-DEFICIENT ALKYNES | C BOND FORMATION | PHASE-TRANSFER CATALYSIS | ALLYLIC DEAROMATIZATION | CHEMISTRY, MULTIDISCIPLINARY | CONJUGATE ADDITION
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14. Full Text Pd(0)-Catalyzed intramolecular arylative dearomatization of β-naphthols
by Xu, Ren-Qi and Yang, Ping and You, Shu-Li
Chemical Communications, ISSN 1359-7345, 2017, Volume 53, Issue 54, pp. 7553 - 7556
An efficient Pd(0)-catalyzed intramolecular arylative dearomatization of beta-naphthols is described. Using Q-Phos as a ligand, the arylative dearomatization... 
ENANTIOSELECTIVE DEAROMATIZATION | GOLD | HYDROXYLATIVE PHENOL DEAROMATIZATION | OXIDATIVE DEAROMATIZATION | CATALYTIC ASYMMETRIC DEAROMATIZATION | CONSTRUCTION | EFFICIENT | CHEMISTRY, MULTIDISCIPLINARY | INDOLES | ACCESS | SKELETON | Catalysts | Ligands | Feasibility
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15. Full Text Construction of the Benzomesembrine Skeleton: Palladium(0)‐Catalyzed Intermolecular Arylative Dearomatization of α‐Naphthols and Subsequent Aza‐Michael Reaction
by Xu, Ren‐Qi and Gu, Qing and You, Shu‐Li
Angewandte Chemie International Edition, ISSN 1433-7851, 06/2017, Volume 56, Issue 25, pp. 7252 - 7256
A novel palladium(0)‐catalyzed intermolecular arylative dearomatization of α‐naphthols and subsequent aza‐Michael reaction is described. Two adjacent... 
cross-coupling | palladium | heterocycles | cyclization | dearomatization | ENANTIOSELECTIVE DEAROMATIZATION | BETA-NAPHTHOLS | ASYMMETRIC DEAROMATIZATION | HYDROXYLATIVE PHENOL DEAROMATIZATION | C-O BOND | SCELETIUM ALKALOIDS | INTRAMOLECULAR DEAROMATIZATION | CHEMISTRY, MULTIDISCIPLINARY | ARYL HALIDES | DIARYL ETHERS | DERIVATIVES | Construction | Palladium | Chemical synthesis | Michael reaction
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