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For: Bauer MR, Di Fruscia P, Lucas SCC, Michaelides IN, Nelson JE, Storer RI, Whitehurst BC. Put a ring on it: application of small aliphatic rings in medicinal chemistry. RSC Med Chem 2021;12:448-71. [PMID: 33937776 DOI: 10.1039/d0md00370k] [Cited by in Crossref: 16] [Cited by in F6Publishing: 45] [Article Influence: 16.0] [Reference Citation Analysis]
Number Citing Articles
1 Rivera G, De Angelis L, Al-Sayyed A, Biswas S, Arman H, Doyle MP. Synthesis of 1,2,3-Triazine Derivatives by Deoxygenation of 1,2,3-Triazine 1-Oxides. Org Lett 2022. [PMID: 36054906 DOI: 10.1021/acs.orglett.2c02484] [Reference Citation Analysis]
2 Wang MM, Nguyen TVT, Waser J. Activation of aminocyclopropanes via radical intermediates. Chem Soc Rev 2022;51:7344-57. [PMID: 35938356 DOI: 10.1039/d2cs00090c] [Reference Citation Analysis]
3 Zeng YF, Wu JB, Chen JT, Guo Y, Wang Z. Oxidative functionalization of alkylidenecyclopropanes and alkylidenecyclobutanes: a versatile platform to access nitrated cyclopropanes and cyclobutanes. Org Biomol Chem 2022. [PMID: 36006008 DOI: 10.1039/d2ob01426b] [Reference Citation Analysis]
4 Majhi J, Dhungana RK, Rentería-Gómez Á, Sharique M, Li L, Dong W, Gutierrez O, Molander GA. Metal-Free Photochemical Imino-Alkylation of Alkenes with Bifunctional Oxime Esters. J Am Chem Soc 2022. [PMID: 35984388 DOI: 10.1021/jacs.2c07170] [Reference Citation Analysis]
5 Ertl P, Altmann E, Racine S, Lewis R. Ring replacement recommender: Ring modifications for improving biological activity. European Journal of Medicinal Chemistry 2022;238:114483. [DOI: 10.1016/j.ejmech.2022.114483] [Reference Citation Analysis]
6 Shi J, Xu QL, Ni YQ, Li L, Pan F. Radical Multicomponent Alkyl Alkynylation of Propellane via Synergistic Photoredox and Copper Catalysis. Org Lett 2022;24:4609-14. [PMID: 35726904 DOI: 10.1021/acs.orglett.2c01721] [Reference Citation Analysis]
7 Li Q, Li L, Xu QL, Pan F. Radical Acylation of [1.1.1]Propellane with Aldehydes: Synthesis of Bicyclo[1.1.1]pentane Ketones. Org Lett 2022. [PMID: 35658457 DOI: 10.1021/acs.orglett.2c01707] [Reference Citation Analysis]
8 Ma J, Chen S, Bellotti P, Wagener T, Daniliuc C, Houk KN, Glorius F. Facile access to fused 2D/3D rings via intermolecular cascade dearomative [2 + 2] cycloaddition/rearrangement reactions of quinolines with alkenes. Nat Catal 2022;5:405-13. [DOI: 10.1038/s41929-022-00784-5] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 4.0] [Reference Citation Analysis]
9 Sharique M, Majhi J, Dhungana RK, Kammer LM, Krumb M, Lipp A, Romero E, Molander GA. A practical and sustainable two-component Minisci alkylation via photo-induced EDA-complex activation. Chem Sci 2022;13:5701-6. [PMID: 35694363 DOI: 10.1039/d2sc01363k] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
10 Gutiérrez-Bonet Á, Popov S, Emmert MH, Hughes JME, Nolting AF, Ruccolo S, Wang Y. Asymmetric Synthesis of Tertiary and Secondary Cyclopropyl Boronates via Cyclopropanation of Enantioenriched Alkenyl Boronic Esters. Org Lett 2022. [PMID: 35544734 DOI: 10.1021/acs.orglett.2c01018] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
11 Stafford NP, Cheng MJ, Dinh DN, Verboom KL, Krische MJ. Chiral α-Stereogenic Oxetanols and Azetidinols via Alcohol-Mediated Reductive Coupling of Allylic Acetates: Enantiotopic π-Facial Selection in Symmetric Ketone Addition. ACS Catal . [DOI: 10.1021/acscatal.2c01647] [Reference Citation Analysis]
12 Lv XY, Abrams R, Martin R. Dihydroquinazolinones as adaptative C(sp3) handles in arylations and alkylations via dual catalytic C-C bond-functionalization. Nat Commun 2022;13:2394. [PMID: 35504911 DOI: 10.1038/s41467-022-29984-0] [Reference Citation Analysis]
13 Blackmun DE, Chamness SA, Schindler CS. Intramolecular, Visible-Light-Mediated Aza Paternò-Büchi Reactions of Unactivated Alkenes. Org Lett 2022. [PMID: 35439412 DOI: 10.1021/acs.orglett.2c01008] [Reference Citation Analysis]
14 Hui C, Wang Z, Xie Y, Liu J. Contemporary synthesis of bioactive cyclobutane natural products. Green Synthesis and Catalysis 2022. [DOI: 10.1016/j.gresc.2022.04.006] [Reference Citation Analysis]
15 Meyer CC, Dubey ZJ, Krische MJ. Enantioselective Iridium-Catalyzed Reductive Coupling of Dienes with Oxetanones and N-Acyl-Azetidinones Mediated by 2-Propanol. Angew Chem Int Ed Engl 2022;61:e202115959. [PMID: 35119714 DOI: 10.1002/anie.202115959] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [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] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 3.0] [Reference Citation Analysis]
17 Lichtenstein YI, Golovanov IS, Ioffe SL, Tabolin AA. Tandem [3+2]-cycloaddition/homo-Baldwin rearrangement of silyl nitronates and donor-acceptor cyclopropenes. A novel approach to polysubstituted aziridines starting from nitro compounds. Tetrahedron 2022. [DOI: 10.1016/j.tet.2022.132693] [Reference Citation Analysis]
18 Mills LR, Gygi D, Ludwig JR, Simmons EM, Wisniewski SR, Kim J, Chirik PJ. Cobalt-Catalyzed C(sp 2 )–C(sp 3 ) Suzuki–Miyaura Cross-Coupling Enabled by Well-Defined Precatalysts with L,X-Type Ligands. ACS Catal 2022;12:1905-18. [DOI: 10.1021/acscatal.1c05586] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
19 Chang TY, Adrion DM, Meyer AR, Lopez SA, Garcia-Garibay MA. A Green Chemistry Approach toward the Stereospecific Synthesis of Densely Functionalized Cyclopropanes via the Solid-State Photodenitrogenation of Crystalline 1-Pyrazolines. J Org Chem 2022. [PMID: 35041410 DOI: 10.1021/acs.joc.1c01808] [Reference Citation Analysis]
20 Goetzke FW, Sidera M, Fletcher SP. Catalytic asymmetric hydrometallation of cyclobutenes with salicylaldehydes. Chem Sci 2021;13:236-40. [DOI: 10.1039/d1sc06035j] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
21 Kelly CB, Milligan JA, Tilley LJ, Sodano TM. Bicyclobutanes: from curiosities to versatile reagents and covalent warheads. Chem Sci . [DOI: 10.1039/d2sc03948f] [Reference Citation Analysis]
22 Sivanandan ST, Bharath Krishna R, Baiju TV, Mohan C. Visible‐Light‐Mediated Ring‐Opening Reactions of Cyclopropanes. European J Organic Chem 2021;2021:6781-805. [DOI: 10.1002/ejoc.202100986] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
23 Mousseau JJ, Perry MA, Bundesmann MW, Chinigo GM, Choi C, Gallego G, Hicklin RW, Hoy S, Limburg DC, Sach NW, Zhang Y. Automated Nanomole-Scale Reaction Screening toward Benzoate Bioisosteres: A Photocatalyzed Approach to Highly Elaborated Bicyclo[1.1.1]Pentanes. ACS Catal 2022;12:600-6. [DOI: 10.1021/acscatal.1c05076] [Cited by in Crossref: 3] [Article Influence: 3.0] [Reference Citation Analysis]
24 Laidlaw G, Franckevičius V. Palladium-Catalyzed Decarboxylative Asymmetric Allylic Alkylation of Thietane 1,1-Dioxides. Org Lett 2021. [PMID: 34914384 DOI: 10.1021/acs.orglett.1c04075] [Reference Citation Analysis]
25 Anderson JM, Measom ND, Murphy JA, Poole DL. Bridge Functionalisation of Bicyclo[1.1.1]pentane Derivatives. Angew Chem 2021;133:24958-73. [DOI: 10.1002/ange.202106352] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
26 Beromi MM, Younker JM, Zhong H, Pabst TP, Chirik PJ. Catalyst Design Principles Enabling Intermolecular Alkene-Diene [2+2] Cycloaddition and Depolymerization Reactions. J Am Chem Soc 2021;143:17793-805. [PMID: 34652908 DOI: 10.1021/jacs.1c08912] [Reference Citation Analysis]
27 Wearing ER, Blackmun DE, Becker MR, Schindler CS. 1- and 2-Azetines via Visible Light-Mediated [2 + 2]-Cycloadditions of Alkynes and Oximes. J Am Chem Soc 2021;143:16235-42. [PMID: 34570970 DOI: 10.1021/jacs.1c07523] [Cited by in Crossref: 3] [Article Influence: 3.0] [Reference Citation Analysis]
28 Yang Y, Tsien J, Hughes JME, Peters BK, Merchant RR, Qin T. An intramolecular coupling approach to alkyl bioisosteres for the synthesis of multisubstituted bicycloalkyl boronates. Nat Chem 2021;13:950-5. [PMID: 34584254 DOI: 10.1038/s41557-021-00786-z] [Cited by in Crossref: 1] [Cited by in F6Publishing: 12] [Article Influence: 1.0] [Reference Citation Analysis]
29 Badir SO, Lipp A, Krumb M, Cabrera-Afonso MJ, Kammer LM, Wu VE, Huang M, Csakai A, Marcaurelle LA, Molander GA. Photoredox-mediated hydroalkylation and hydroarylation of functionalized olefins for DNA-encoded library synthesis. Chem Sci 2021;12:12036-45. [PMID: 34667569 DOI: 10.1039/d1sc03191k] [Cited by in Crossref: 2] [Cited by in F6Publishing: 11] [Article Influence: 2.0] [Reference Citation Analysis]
30 K. Pagire S, Kumagai N, Shibasaki M. Highly Enantio- and Diastereoselective Synthesis of 1,2,3-Trisubstituted Cyclopropanes from α,β-Unsaturated Amides and Stabilized Sulfur Ylides Catalyzed by a Chiral Copper(I) Complex. ACS Catal 2021;11:11597-606. [DOI: 10.1021/acscatal.1c02723] [Reference Citation Analysis]
31 Goetz AE, Becirovic H, Blasberg F, Chen B, Clarke HJ, Colombo M, Daddario P, Damon DB, Depretz C, Dumond YR, Grilli MD, Han L, Houck TL, Johnson AM, Jones KN, Jung J, Leeman M, Liu F, Lu CV, Mangual EJ, Nelson JD, Puchlopek-dermenci ALA, Ruggeri SG, Simonds PA, Sitter B, Virtue DE, Wang S, Yu L, Yu T. Large-Scale Cyclopropanation of Butyl Acrylate with Difluorocarbene and Classical Resolution of a Key Fluorinated Building Block. Org Process Res Dev . [DOI: 10.1021/acs.oprd.1c00171] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
32 Biernasiuk A, Banasiewicz A, Masłyk M, Martyna A, Janeczko M, Baranowska-Łączkowska A, Malm A, Łączkowski KZ. Synthesis and Physicochemical Characterization of Novel Dicyclopropyl-Thiazole Compounds as Nontoxic and Promising Antifungals. Materials (Basel) 2021;14:3500. [PMID: 34201678 DOI: 10.3390/ma14133500] [Reference Citation Analysis]
33 Zhong X, Tan J, Qiao J, Zhou Y, Lv C, Su Z, Dong S, Feng X. Catalytic asymmetric synthesis of spirocyclobutyl oxindoles and beyond via [2+2] cycloaddition and sequential transformations. Chem Sci 2021;12:9991-7. [PMID: 34377393 DOI: 10.1039/d1sc02681j] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
34 Brown MS, Caporello MA, Goetz AE, Johnson AM, Jones KN, Knopf KM, Kulkarni SA, Lee T, Li B, Lu CV, Magano J, Puchlopek-dermenci ALA, Reyes GP, Ruggeri SG, Wei L, Weisenburger GA, Wisdom RA, Zhang M. Streamlined Synthesis of a Bicyclic Amine Moiety Using an Enzymatic Amidation and Identification of a Novel Solid Form. Org Process Res Dev 2021;25:1419-30. [DOI: 10.1021/acs.oprd.1c00120] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
35 Serafini M, Cargnin S, Massarotti A, Tron GC, Pirali T, Genazzani AA. What's in a Name? Drug Nomenclature and Medicinal Chemistry Trends using INN Publications. J Med Chem 2021;64:4410-29. [PMID: 33847110 DOI: 10.1021/acs.jmedchem.1c00181] [Reference Citation Analysis]
36 Ratni H, Baumann K, Bellotti P, Cook XA, Green LG, Luebbers T, Reutlinger M, Stepan AF, Vifian W. Phenyl bioisosteres in medicinal chemistry: discovery of novel γ-secretase modulators as a potential treatment for Alzheimer's disease. RSC Med Chem 2021;12:758-66. [PMID: 34124674 DOI: 10.1039/d1md00043h] [Cited by in F6Publishing: 3] [Reference Citation Analysis]