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For: Flick AC, Ding HX, Leverett CA, Fink SJ, O’donnell CJ. Synthetic Approaches to New Drugs Approved During 2016. J Med Chem 2018;61:7004-31. [DOI: 10.1021/acs.jmedchem.8b00260] [Cited by in Crossref: 28] [Cited by in F6Publishing: 21] [Article Influence: 7.0] [Reference Citation Analysis]
Number Citing Articles
1 Flick AC, Leverett CA, Ding HX, Mcinturff E, Fink SJ, Helal CJ, Deforest JC, Morse PD, Mahapatra S, O’donnell CJ. Synthetic Approaches to New Drugs Approved during 2018. J Med Chem 2020;63:10652-704. [DOI: 10.1021/acs.jmedchem.0c00345] [Cited by in Crossref: 9] [Cited by in F6Publishing: 4] [Article Influence: 4.5] [Reference Citation Analysis]
2 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]
3 Abourehab MAS, Alqahtani AM, Youssif BGM, Gouda AM. Globally Approved EGFR Inhibitors: Insights into Their Syntheses, Target Kinases, Biological Activities, Receptor Interactions, and Metabolism. Molecules 2021;26:6677. [PMID: 34771085 DOI: 10.3390/molecules26216677] [Reference Citation Analysis]
4 Flick AC, Leverett CA, Ding HX, Mcinturff E, Fink SJ, Helal CJ, O’donnell CJ. Synthetic Approaches to the New Drugs Approved During 2017. J Med Chem 2019;62:7340-82. [DOI: 10.1021/acs.jmedchem.9b00196] [Cited by in Crossref: 23] [Cited by in F6Publishing: 16] [Article Influence: 7.7] [Reference Citation Analysis]
5 Dhameliya TM, Donga HA, Vaghela PV, Panchal BG, Sureja DK, Bodiwala KB, Chhabria MT. A decennary update on applications of metal nanoparticles (MNPs) in the synthesis of nitrogen- and oxygen-containing heterocyclic scaffolds. RSC Adv 2020;10:32740-820. [DOI: 10.1039/d0ra02272a] [Cited by in Crossref: 6] [Article Influence: 3.0] [Reference Citation Analysis]
6 Rísquez-Cuadro R, Matsumoto R, Ortega-Caballero F, Nanba E, Higaki K, García Fernández JM, Ortiz Mellet C. Pharmacological Chaperones for the Treatment of α-Mannosidosis. J Med Chem 2019;62:5832-43. [PMID: 31017416 DOI: 10.1021/acs.jmedchem.9b00153] [Cited by in Crossref: 13] [Cited by in F6Publishing: 12] [Article Influence: 4.3] [Reference Citation Analysis]
7 Prasad V, Mishra N, Agrahari AK, Singh SK, Mohapatra PP, Tiwari VK. Cycloelimination-assisted Combinatorial Synthesis of Diverse Heterocyclic Scaffolds of Chemotherapeutic Values. COC 2019;23:768-808. [DOI: 10.2174/1385272823666190405145805] [Cited by in Crossref: 2] [Article Influence: 0.7] [Reference Citation Analysis]
8 Robello M, Barresi E, Baglini E, Salerno S, Taliani S, Settimo FD. The Alpha Keto Amide Moiety as a Privileged Motif in Medicinal Chemistry: Current Insights and Emerging Opportunities. J Med Chem 2021;64:3508-45. [PMID: 33764065 DOI: 10.1021/acs.jmedchem.0c01808] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
9 Luo G, Xiang M, Krische MJ. Successive Nucleophilic and Electrophilic Allylation for the Catalytic Enantioselective Synthesis of 2,4-Disubstituted Pyrrolidines. Org Lett 2019;21:2493-7. [PMID: 30816719 DOI: 10.1021/acs.orglett.9b00508] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
10 Ge C, Wang G, Wu P, Chen C. Synthesis of Naphthalenyl Triflates via the Cationic Annulation of Benzodiynes with Triflic Acid. Org Lett 2019;21:5010-4. [DOI: 10.1021/acs.orglett.9b01590] [Cited by in Crossref: 6] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
11 Flick AC, Leverett CA, Ding HX, McInturff E, Fink SJ, Mahapatra S, Carney DW, Lindsey EA, DeForest JC, France SP, Berritt S, Bigi-Botterill SV, Gibson TS, Liu Y, O'Donnell CJ. Synthetic Approaches to the New Drugs Approved during 2019. J Med Chem 2021;64:3604-57. [PMID: 33783211 DOI: 10.1021/acs.jmedchem.1c00208] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
12 Wang S, Yuan XH, Wang SQ, Zhao W, Chen XB, Yu B. FDA-approved pyrimidine-fused bicyclic heterocycles for cancer therapy: Synthesis and clinical application. Eur J Med Chem 2021;214:113218. [PMID: 33540357 DOI: 10.1016/j.ejmech.2021.113218] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 3.0] [Reference Citation Analysis]
13 Hartwig JF, Shaughnessy KH, Shekhar S, Green RA. Palladium‐Catalyzed Amination of Aryl Halides. Organic Reactions. Wiley; 2004. pp. 853-958. [DOI: 10.1002/0471264180.or100.14] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
14 Cai Q, Zhou W. Ullmann‐Ma Reaction: Development, Scope and Applications in Organic Synthesis . Chin J Chem 2020;38:879-93. [DOI: 10.1002/cjoc.202000075] [Cited by in Crossref: 23] [Cited by in F6Publishing: 4] [Article Influence: 11.5] [Reference Citation Analysis]
15 Li B, Shen Y, Wu H, Wu X, Yuan L, Ji Q. Design, synthesis and biological evaluation of novel 3,4-dihydro-2(1H)-quinolinone derivatives as potential chitin synthase inhibitors and antifungal agents. European Journal of Medicinal Chemistry 2020;195:112278. [DOI: 10.1016/j.ejmech.2020.112278] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
16 Rodrigalvarez J, Reeve LA, Miró J, Gaunt MJ. Pd(II)-Catalyzed Enantioselective C(sp3)-H Arylation of Cyclopropanes and Cyclobutanes Guided by Tertiary Alkylamines. J Am Chem Soc 2022. [PMID: 35212219 DOI: 10.1021/jacs.1c11921] [Reference Citation Analysis]
17 Nikolaienko P, Jentsch M, Kale AP, Cai Y, Rueping M. Electrochemical and Scalable Dehydrogenative C(sp 3 )−H Amination via Remote Hydrogen Atom Transfer in Batch and Continuous Flow. Chem Eur J 2019;25:7177-84. [DOI: 10.1002/chem.201806092] [Cited by in Crossref: 20] [Cited by in F6Publishing: 12] [Article Influence: 6.7] [Reference Citation Analysis]
18 Loui HJ, Suneja A, Schneider C. Cooperative Rh/Chiral Phosphoric Acid Catalysis toward the Highly Stereoselective (3 + 3)-Cycloannulation of Carbonyl Ylides and Indolyl-2-methides. Org Lett 2021;23:2578-83. [DOI: 10.1021/acs.orglett.1c00489] [Cited by in Crossref: 4] [Cited by in F6Publishing: 1] [Article Influence: 4.0] [Reference Citation Analysis]
19 Kobayashi S, Tamura T, Yoshimoto S, Kawakami T, Masuyama A. 4-Methyltetrahydropyran (4-MeTHP): Application as an Organic Reaction Solvent. Chem Asian J 2019;14:3921-37. [PMID: 31549485 DOI: 10.1002/asia.201901169] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 1.7] [Reference Citation Analysis]
20 Ghanakota P, Bos PH, Konze KD, Staker J, Marques G, Marshall K, Leswing K, Abel R, Bhat S. Combining Cloud-Based Free-Energy Calculations, Synthetically Aware Enumerations, and Goal-Directed Generative Machine Learning for Rapid Large-Scale Chemical Exploration and Optimization. J Chem Inf Model 2020;60:4311-25. [DOI: 10.1021/acs.jcim.0c00120] [Cited by in Crossref: 8] [Cited by in F6Publishing: 6] [Article Influence: 4.0] [Reference Citation Analysis]
21 Wang S, Yu B, Liu H. Pd(II)-Catalyzed Intramolecular C(sp 2 )–H Arylation of Tryptamines Using the Nonsteric NH 2 as a Directing Group. Org Lett 2021;23:42-8. [DOI: 10.1021/acs.orglett.0c03668] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
22 Ning L, Li H, Lai Z, Szostak M, Chen X, Dong Y, Jin S, An J. Synthesis of α-Deuterated Primary Amines via Reductive Deuteration of Oximes Using D2O as a Deuterium Source. J Org Chem 2021;86:2907-16. [PMID: 33486945 DOI: 10.1021/acs.joc.0c02829] [Reference Citation Analysis]
23 Ötvös SB, Kappe CO. Continuous flow asymmetric synthesis of chiral active pharmaceutical ingredients and their advanced intermediates. Green Chem 2021;23:6117-38. [PMID: 34671222 DOI: 10.1039/d1gc01615f] [Cited by in Crossref: 3] [Article Influence: 3.0] [Reference Citation Analysis]
24 Li H, Hou Y, Liu C, Lai Z, Ning L, Szostak R, Szostak M, An J. Pentafluorophenyl Esters: Highly Chemoselective Ketyl Precursors for the Synthesis of α,α-Dideuterio Alcohols Using SmI 2 and D 2 O as a Deuterium Source. Org Lett 2020;22:1249-53. [DOI: 10.1021/acs.orglett.9b04383] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 3.5] [Reference Citation Analysis]
25 Xu W, Gong X, Odilov A, Hu T, Jiang X, Zhu F, Guo S, Jiang D, Wu M, Shen J. Scalable Process for Making 5,7-Dichlorotetrahydroisoquinoline-6-carboxylic Acid Using Methylene as the Protecting Group. Org Process Res Dev 2021;25:2447-52. [DOI: 10.1021/acs.oprd.1c00229] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
26 Mousavi H. A comprehensive survey upon diverse and prolific applications of chitosan-based catalytic systems in one-pot multi-component synthesis of heterocyclic rings. Int J Biol Macromol 2021;186:1003-166. [PMID: 34174311 DOI: 10.1016/j.ijbiomac.2021.06.123] [Reference Citation Analysis]