BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Zhu T, Chen J, Xu M. Rhodium-Catalyzed Enantioselective Addition to Unsymmetrical α-Diketones: Tandem One-Pot Synthesis of Optically Active 3-Tetrasubstituted Isochroman Derivatives. Chem Eur J 2013;19:865-9. [DOI: 10.1002/chem.201203701] [Cited by in Crossref: 32] [Cited by in F6Publishing: 27] [Article Influence: 3.2] [Reference Citation Analysis]
Number Citing Articles
1 Santos CM, Silva AM. Six-Membered Ring Systems. Elsevier; 2014. pp. 463-520. [DOI: 10.1016/b978-0-08-100017-5.00015-7] [Cited by in Crossref: 2] [Article Influence: 0.3] [Reference Citation Analysis]
2 Hu Y, Pan D, Cong L, Yao Y, Yu C, Li T, Yao C. NHC-Catalyzed Efficient Syntheses of Isoquinolinones or Isochromanones through Formal [4+2] Cycloaddition of o -Quinodimethanes with Acylhydrazones or Ketones. ChemistrySelect 2018;3:1708-12. [DOI: 10.1002/slct.201702925] [Cited by in Crossref: 11] [Cited by in F6Publishing: 7] [Article Influence: 2.8] [Reference Citation Analysis]
3 Zhu D, Chen W, Xu M. Rhodium-catalyzed asymmetric intramolecular addition of arylboronic acids to ketones: catalytic enantioselective access to 3-hydroxy-2,3-dihydrobenzofurans bearing a tetrasubstituted carbon stereocenter. Tetrahedron 2016;72:2637-42. [DOI: 10.1016/j.tet.2015.04.030] [Cited by in Crossref: 12] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
4 Wang H, Jiang T, Xu M. Simple Branched Sulfur–Olefins as Chiral Ligands for Rh-Catalyzed Asymmetric Arylation of Cyclic Ketimines: Highly Enantioselective Construction of Tetrasubstituted Carbon Stereocenters. J Am Chem Soc 2013;135:971-4. [DOI: 10.1021/ja3110818] [Cited by in Crossref: 187] [Cited by in F6Publishing: 148] [Article Influence: 20.8] [Reference Citation Analysis]
5 Zhu T, Xu M. Chiral Sulfinamide-Olefin Ligands: Switchable Selectivity in Rhodium-Catalyzed Asymmetric 1,2-Addition of Arylboronic Acids to Aliphatic α -Ketoesters. Chin J Chem 2013;31:321-8. [DOI: 10.1002/cjoc.201300063] [Cited by in Crossref: 16] [Cited by in F6Publishing: 11] [Article Influence: 1.8] [Reference Citation Analysis]
6 Shirai T, Yamamoto Y. Scope and Mechanistic Studies of the Cationic Ir/Me-BIPAM-Catalyzed Asymmetric Intramolecular Direct Hydroarylation Reaction. Organometallics 2015;34:3459-63. [DOI: 10.1021/om501260w] [Cited by in Crossref: 16] [Cited by in F6Publishing: 9] [Article Influence: 2.3] [Reference Citation Analysis]
7 Wu C, Zhang Y, Xu M. Ligand-Controlled Rhodium-Catalyzed Site-Selective Asymmetric Addition of Arylboronic Acids to α,β-Unsaturated Cyclic N -Sulfonyl Ketimines. Org Lett 2018;20:1789-93. [DOI: 10.1021/acs.orglett.8b00289] [Cited by in Crossref: 26] [Cited by in F6Publishing: 15] [Article Influence: 6.5] [Reference Citation Analysis]
8 Li Y, Xu M. Simple sulfur–olefins as new promising chiral ligands for asymmetric catalysis. Chem Commun 2014;50:3771-82. [DOI: 10.1039/c3cc49431d] [Cited by in Crossref: 85] [Cited by in F6Publishing: 11] [Article Influence: 10.6] [Reference Citation Analysis]
9 Zhang Z, Zhu D, Chen W, Xu B, Xu M. Enantioselective Synthesis of gem -Diaryl Benzofuran-3(2 H )-ones via One-Pot Asymmetric Rhodium/Palladium Relay Catalysis. Org Lett 2017;19:2726-9. [DOI: 10.1021/acs.orglett.7b01070] [Cited by in Crossref: 9] [Cited by in F6Publishing: 7] [Article Influence: 1.8] [Reference Citation Analysis]
10 Infante R, Martin-alvarez JM, Andrés C, Nieto J. Dimethylzinc-Mediated Addition of Phenylacetylene to α-Diketones Catalyzed by Chiral Perhydro-1,3-benzoxazines. Org Lett 2017;19:1516-9. [DOI: 10.1021/acs.orglett.7b00252] [Cited by in Crossref: 6] [Cited by in F6Publishing: 4] [Article Influence: 1.2] [Reference Citation Analysis]
11 Tamanna, Kumar M, Joshi K, Chauhan P. Catalytic Asymmetric Synthesis of Isochroman Derivatives. Adv Synth Catal 2020;362:1907-26. [DOI: 10.1002/adsc.202000243] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
12 Yang XC, Xu M, Wang JB, Liu MM, Mathey F, Hua YZ, Wang MC. Enantioselective synthesis of indanone spiro-isochromanone derivatives via a dinuclear zinc-catalyzed Michael/transesterification tandem reaction. Org Biomol Chem 2020;18:3917-26. [PMID: 32400845 DOI: 10.1039/d0ob00541j] [Cited by in Crossref: 4] [Article Influence: 2.0] [Reference Citation Analysis]
13 Sathi V, Deepthi A, Thomas NV. An Unprecedented Synthesis of 3,3‐Disubstituted Isochroman‐1,4‐diones Using Nitrones as Oxygen Atom Donors. J Heterocyclic Chem 2019;56:2333-40. [DOI: 10.1002/jhet.3619] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
14 Wang B, Leng H, Yang X, Han B, Rao C, Liu L, Peng C, Huang W. Efficient synthesis of tetrahydronaphthalene- or isochroman-fused spirooxindoles using tandem reactions. RSC Adv 2015;5:88272-6. [DOI: 10.1039/c5ra15735h] [Cited by in Crossref: 20] [Cited by in F6Publishing: 1] [Article Influence: 2.9] [Reference Citation Analysis]
15 Xue F, Wang D, Li X, Wan B. Chiral olefin–sulfoxide as ligands for rhodium-catalyzed asymmetric conjugate addition of arylboronic acids to unsaturated esters. Org Biomol Chem 2013;11:7893. [DOI: 10.1039/c3ob41342j] [Cited by in Crossref: 21] [Cited by in F6Publishing: 12] [Article Influence: 2.3] [Reference Citation Analysis]
16 Yuan S, Wang Y, Liu J, Qiu G. NBS-Mediated Oxygen Transfer Reaction of Carbonyl in Ester: Efficient Synthesis of Benzil- o -carboxylate Derivative From o -Alkynylbenzoate. Adv Synth Catal 2017;359:1981-9. [DOI: 10.1002/adsc.201700168] [Cited by in Crossref: 23] [Cited by in F6Publishing: 16] [Article Influence: 4.6] [Reference Citation Analysis]
17 Wang Z, Chen W, Xu M. Rhodium-catalyzed Asymmetric Arylation of Nitroalkenes Powered by Simple Chiral Sulfur-Olefin Ligands: Rh-catalyzed Asymmetric Arylation of Nitroalkenes. Journal of the Chinese Chemical Society 2018;65:331-6. [DOI: 10.1002/jccs.201700328] [Cited by in Crossref: 1] [Article Influence: 0.2] [Reference Citation Analysis]
18 Sipos G, Drinkel EE, Dorta R. The emergence of sulfoxides as efficient ligands in transition metal catalysis. Chem Soc Rev 2015;44:3834-60. [PMID: 25954773 DOI: 10.1039/c4cs00524d] [Cited by in Crossref: 130] [Cited by in F6Publishing: 12] [Article Influence: 18.6] [Reference Citation Analysis]
19 Otocka S, Kwiatkowska M, Madalińska L, Kiełbasiński P. Chiral Organosulfur Ligands/Catalysts with a Stereogenic Sulfur Atom: Applications in Asymmetric Synthesis. Chem Rev 2017;117:4147-81. [PMID: 28191933 DOI: 10.1021/acs.chemrev.6b00517] [Cited by in Crossref: 132] [Cited by in F6Publishing: 82] [Article Influence: 26.4] [Reference Citation Analysis]
20 Li Y, Zhu D, Xu M. A new versatile approach to synthesise enantioenriched 3-hydroxyoxindoles, 1,3-dihydroisobenzofuran and 3-isochromanone derivatives by a rhodium-catalyzed asymmetric arylation–cyclization sequence. Chem Commun 2013;49:11659. [DOI: 10.1039/c3cc47927g] [Cited by in Crossref: 28] [Cited by in F6Publishing: 20] [Article Influence: 3.1] [Reference Citation Analysis]
21 Crespi S, Jäger S, König B, Fagnoni M. A Photocatalytic Meerwein Approach to the Synthesis of Isochromanones and Isochromenones: A Photocatalytic Meerwein Approach to the Synthesis of Isochromanones and Isochromenones. Eur J Org Chem 2017;2017:2147-53. [DOI: 10.1002/ejoc.201601458] [Cited by in Crossref: 17] [Cited by in F6Publishing: 6] [Article Influence: 3.4] [Reference Citation Analysis]
22 Liu Y, Li W, Zhang J. Chiral ligands designed in China. National Science Review 2017;4:326-58. [DOI: 10.1093/nsr/nwx064] [Cited by in Crossref: 37] [Cited by in F6Publishing: 24] [Article Influence: 7.4] [Reference Citation Analysis]
23 Shimogaki M, Fujita M, Sugimura T. Enantioselective Oxidation of Alkenylbenzoates Catalyzed by Chiral Hypervalent Iodine(III) To Yield 4-Hydroxyisochroman-1-ones: Enantioselective Oxidation of Alkenylbenzoates. Eur J Org Chem 2013;2013:7128-38. [DOI: 10.1002/ejoc.201300959] [Cited by in Crossref: 64] [Cited by in F6Publishing: 45] [Article Influence: 7.1] [Reference Citation Analysis]
24 Solé D, Mariani F, Fernández I. A Joint Experimental-Computational Comparative Study of the Pd 0 -Catalysed Reactions of Aryl Iodides and Aldehydes with N, O, and S Tethers: Pd 0 -Catalysed Reactions of Aryl Iodides and Aldehydes. Eur J Org Chem 2015;2015:3935-42. [DOI: 10.1002/ejoc.201500393] [Cited by in Crossref: 8] [Cited by in F6Publishing: 3] [Article Influence: 1.1] [Reference Citation Analysis]
25 Dong H, Xu M, Feng C, Sun X, Lin G. Recent applications of chiral N-tert-butanesulfinyl imines, chiral diene ligands and chiral sulfur–olefin ligands in asymmetric synthesis. Org Chem Front 2015;2:73-89. [DOI: 10.1039/c4qo00245h] [Cited by in Crossref: 52] [Article Influence: 7.4] [Reference Citation Analysis]
26 Wang H, Li Y, Xu M. Rhodium-Catalyzed Highly Enantioselective Arylation of Cyclic Diketimines: Efficient Synthesis of Chiral Tetrasubstituted 1,2,5-Thiadiazoline 1,1-Dioxides. Org Lett 2014;16:3962-5. [DOI: 10.1021/ol501770q] [Cited by in Crossref: 52] [Cited by in F6Publishing: 39] [Article Influence: 6.5] [Reference Citation Analysis]
27 Chen WW, Xu MH. Recent advances in rhodium-catalyzed asymmetric synthesis of heterocycles. Org Biomol Chem 2017;15:1029-50. [PMID: 27808318 DOI: 10.1039/c6ob02021f] [Cited by in Crossref: 39] [Cited by in F6Publishing: 3] [Article Influence: 9.8] [Reference Citation Analysis]
28 Yu Y, Xu M. Design of a new series of chiral phosphite–olefin ligands and their application in asymmetric catalysis. Org Chem Front 2014;1:738. [DOI: 10.1039/c4qo00135d] [Cited by in Crossref: 18] [Article Influence: 2.3] [Reference Citation Analysis]