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For: Benmekhbi L, Louafi F, Roisnel T, Hurvois JP. Synthesis of Tetrahydroisoquinoline Alkaloids and Related Compounds through the Alkylation of Anodically Prepared α-Amino Nitriles. J Org Chem 2016;81:6721-39. [PMID: 27410716 DOI: 10.1021/acs.joc.6b01419] [Cited by in Crossref: 24] [Cited by in F6Publishing: 14] [Article Influence: 4.0] [Reference Citation Analysis]
Number Citing Articles
1 Yang Y, Li Y, Cheng C, Yang G, Zhang J, Zhang Y, Zhao Y, Zhang L, Li C, Tang L. Synthesis of 4-Aryl Isoquinolinedione Derivatives by a Palladium-Catalyzed Coupling Reaction of Aryl Halides with Isoquinoline-1,3(2 H,4 H)-diones. J Org Chem 2018;83:3348-53. [PMID: 29400968 DOI: 10.1021/acs.joc.7b02961] [Cited by in Crossref: 9] [Cited by in F6Publishing: 6] [Article Influence: 2.3] [Reference Citation Analysis]
2 Lv J, Li ZH, Deng AJ, Qin HL. A unified total synthesis of benzo[d][1,3]dioxole-type benzylisoquinoline alkaloids of aporphines, coptisines, and dibenzopyrrocolines. Org Biomol Chem 2021. [PMID: 34951439 DOI: 10.1039/d1ob02258j] [Reference Citation Analysis]
3 Kouznetsov VV, Galvis CEP. Strecker reaction and α-amino nitriles: Recent advances in their chemistry, synthesis, and biological properties. Tetrahedron 2018;74:773-810. [DOI: 10.1016/j.tet.2018.01.005] [Cited by in Crossref: 73] [Cited by in F6Publishing: 28] [Article Influence: 18.3] [Reference Citation Analysis]
4 Liu P, Zhang C, Zhao S, Yu F, Li F, He Y. Metal-Free Aerobic Oxidative Cyanation of Tertiary Amines: Azobis(isobutyronitrile) (AIBN) as a Sole Cyanide Source. J Org Chem 2017;82:12786-90. [DOI: 10.1021/acs.joc.7b02021] [Cited by in Crossref: 14] [Cited by in F6Publishing: 7] [Article Influence: 2.8] [Reference Citation Analysis]
5 Zhuang SY, Tang YX, Liu JY, Chen XL, Ma JT, Wu YD, Zheng KL, Wu AX. I2-DMSO-Mediated N-H/α-C(sp3)-H Difunctionalization of Tetrahydroisoquinoline: Formal [2 + 2 + 1] Annulation for the Construction of Pyrrolo[2,1-a]isoquinoline Derivatives. Org Lett 2022. [PMID: 35394795 DOI: 10.1021/acs.orglett.2c00813] [Reference Citation Analysis]
6 Talk RA, El-tunsi A, Robertson CC, Coldham I. Regioselective Lithiation and Electrophilic Quenching of N -Boc-3-phenyltetrahydroisoquinoline: Regioselective Lithiation and Electrophilic Quenching of N -Boc-3-phenyltetrahydroisoquinoline. Eur J Org Chem 2019;2019:5294-301. [DOI: 10.1002/ejoc.201900238] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
7 Kouznetsov VV, Ortiz-villamizar MC, Méndez-vargas LY, Galvis CEP. A Review on Metal-Free Oxidative α-Cyanation and Alkynylation of N-Substituted Tetrahydroisoquinolines as a Rapid Route for the Synthesis of Isoquinoline Alkaloids. COC 2020;24:809-16. [DOI: 10.2174/1385272824999200420073539] [Cited by in Crossref: 6] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
8 Hill JE, Matlock JV, Lefebvre Q, Cooper KG, Clayden J. Consecutive Ring Expansion and Contraction for the Synthesis of 1-Aryl Tetrahydroisoquinolines and Tetrahydrobenzazepines from Readily Available Heterocyclic Precursors. Angew Chem Int Ed Engl 2018;57:5788-91. [PMID: 29539221 DOI: 10.1002/anie.201802188] [Cited by in Crossref: 24] [Cited by in F6Publishing: 13] [Article Influence: 6.0] [Reference Citation Analysis]
9 Li YX, Cheng C, Tang L, Yang YY. Palladium catalyzed asymmetric allylic alkylation of isoquinolinedione derivatives in the preparation of quaternary carbon stereocenters. Org Biomol Chem 2020;18:4551-5. [PMID: 32484497 DOI: 10.1039/d0ob00765j] [Cited by in Crossref: 3] [Article Influence: 1.5] [Reference Citation Analysis]
10 Kim HP, Yu H, Kim H, Kim SH, Lee D. DDQ-Promoted Mild and Efficient Metal-Free Oxidative α-Cyanation of N-Acyl/Sulfonyl 1,2,3,4-Tetrahydroisoquinolines. Molecules 2018;23:E3223. [PMID: 30563272 DOI: 10.3390/molecules23123223] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 0.8] [Reference Citation Analysis]
11 Balzano F, Uccello-barretta G, Aiello F. Chiral Analysis by NMR Spectroscopy: Chiral Solvating Agents. Chiral Analysis. Elsevier; 2018. pp. 367-427. [DOI: 10.1016/b978-0-444-64027-7.00009-4] [Cited by in Crossref: 7] [Article Influence: 1.8] [Reference Citation Analysis]
12 Wu Z, Du S, Gao G, Yang W, Yang X, Huang H, Chang M. Secondary amines as coupling partners in direct catalytic asymmetric reductive amination. Chem Sci 2019;10:4509-14. [PMID: 31057780 DOI: 10.1039/c9sc00323a] [Cited by in Crossref: 19] [Cited by in F6Publishing: 1] [Article Influence: 6.3] [Reference Citation Analysis]
13 Das E, Basak S, Anoop A, Chand S, Basak A. How To Achieve High Regioselectivity in Barrier-less Nucleophilic Addition to p -Benzynes Generated via Bergman Cyclization of Unsymmetrical Cyclic Azaenediyne? J Org Chem 2019;84:2911-21. [DOI: 10.1021/acs.joc.9b00060] [Cited by in Crossref: 6] [Article Influence: 2.0] [Reference Citation Analysis]
14 Hu Z, Tang H, Yan X, Zeng Y, Aisa HA, Zhang Y, Hao X. Five new alkaloids from Aconitum apetalum (Ranunculaceae). Phytochemistry Letters 2019;29:6-11. [DOI: 10.1016/j.phytol.2018.10.017] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
15 Ma RJ, Sun JT, Liu CH, Chen L, Si CM, Wei BG. Synthesis of 1-benzylisoindoline and 1-benzyl-tetrahydroisoquinoline through nucleophilic addition of organozinc reagents to N,O-acetals. Org Biomol Chem 2020;18:7139-50. [PMID: 32966517 DOI: 10.1039/d0ob01477j] [Cited by in Crossref: 4] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
16 Kuwabara K, Maekawa Y, Murai T. P-stereogenic phosphinothioic acids, phosphonothioic acids and their esters: Syntheses, reactions, and applications. Tetrahedron 2020;76:131152. [DOI: 10.1016/j.tet.2020.131152] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
17 Gunasekera D, Mahajan JP, Wanzi Y, Rodrigo S, Liu W, Tan T, Luo L. Controlling One- or Two-Electron Oxidation for Selective Amine Functionalization by Alternating Current Frequency. J Am Chem Soc 2022. [PMID: 35622985 DOI: 10.1021/jacs.2c02605] [Reference Citation Analysis]
18 Buev EM, Stepanov MA, Moshkin VS, Sosnovskikh VY. Synthesis of 6,12-Methanodibenzo[ c , f ]azocines and 4-Aryltetrahydroisoquinolines from Aromatic Aldehydes. Org Lett 2020;22:631-5. [DOI: 10.1021/acs.orglett.9b04401] [Cited by in Crossref: 5] [Cited by in F6Publishing: 2] [Article Influence: 1.7] [Reference Citation Analysis]
19 Mattalia JR. The reductive decyanation reaction: an overview and recent developments. Beilstein J Org Chem 2017;13:267-84. [PMID: 28326136 DOI: 10.3762/bjoc.13.30] [Cited by in Crossref: 32] [Cited by in F6Publishing: 27] [Article Influence: 6.4] [Reference Citation Analysis]
20 Du Q, Liu L, Zhou T. General and Efficient Copper-Catalyzed Oxazaborolidine Complex in Transfer Hydrogenation of Isoquinolines under Mild Conditions. ACS Omega 2020;5:21219-25. [PMID: 32875258 DOI: 10.1021/acsomega.0c02957] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
21 Hill JE, Matlock JV, Lefebvre Q, Cooper KG, Clayden J. Consecutive Ring Expansion and Contraction for the Synthesis of 1-Aryl Tetrahydroisoquinolines and Tetrahydrobenzazepines from Readily Available Heterocyclic Precursors. Angew Chem 2018;130:5890-3. [DOI: 10.1002/ange.201802188] [Cited by in Crossref: 10] [Article Influence: 2.5] [Reference Citation Analysis]
22 Ji Y, Feng G, Chen M, Shi L, Du H, Zhou Y. Iridium-catalyzed asymmetric hydrogenation of cyclic iminium salts. Org Chem Front 2017;4:1125-9. [DOI: 10.1039/c7qo00060j] [Cited by in Crossref: 17] [Cited by in F6Publishing: 1] [Article Influence: 3.4] [Reference Citation Analysis]
23 Motaleb A, Bera A, Maity P. An organocatalyst bound α-aminoalkyl radical intermediate for controlled aerobic oxidation of iminium ions. Org Biomol Chem 2018;16:5081-5. [PMID: 29947387 DOI: 10.1039/c8ob01032c] [Cited by in Crossref: 17] [Cited by in F6Publishing: 2] [Article Influence: 5.7] [Reference Citation Analysis]