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For: Biletskyi B, Colonna P, Masson K, Parrain JL, Commeiras L, Chouraqui G. Small rings in the bigger picture: ring expansion of three- and four-membered rings to access larger all-carbon cyclic systems. Chem Soc Rev 2021;50:7513-38. [PMID: 34002179 DOI: 10.1039/d0cs01396j] [Cited by in Crossref: 5] [Cited by in F6Publishing: 1] [Article Influence: 5.0] [Reference Citation Analysis]
Number Citing Articles
1 Guo Z, Li K, Li H, Wang X, Zhang J, Xie M. Acid‐Promoted Carbon‐Carbon Triple Bond Cleavage of Ynones for the Synthesis of Benzo[ d ]oxazoles/Benzo[ d ]thiazoles and 1‐Arylethan‐1‐ones. Eur J Org Chem 2022;2022. [DOI: 10.1002/ejoc.202200858] [Reference Citation Analysis]
2 Jia S, Tian Y, Li X, Wang P, Lan Y, Yan H. Atroposelective Construction of Nine-Membered Carbonate-Bridged Biaryls. Angew Chem Int Ed Engl 2022;61:e202206501. [PMID: 35621411 DOI: 10.1002/anie.202206501] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
3 Prakash M, Rani P, Samanta S. A substrate-dependent reaction of 1-aryl-2-alkyl-1,2-diketones with 2-aroyl-1-chlorocyclopropanecarboxylates: selective access to 2',5'-dicyclopropoxy-1,1':4',1''-teraryls and pentafulvenes. Org Biomol Chem 2022. [PMID: 35894220 DOI: 10.1039/d2ob00971d] [Reference Citation Analysis]
4 Meyer S, Göbel L, Livingstone K, Roblick C, Daniliuc CG, Gilmour RA. Cyclopropene activation via I(I)/I(III) catalysis: Proof of principle and application in direct tetrafluorination. Tetrahedron 2022. [DOI: 10.1016/j.tet.2022.132925] [Reference Citation Analysis]
5 Zhang F, Dai X, Dai L, Zheng W, Chan WL, Tang X, Zhang X, Lu Y. Phosphine-Catalyzed Enantioselective (3+2) Annulation of Vinylcyclopropanes with Imines for the Synthesis of Chiral Pyrrolidines. Angew Chem Int Ed Engl 2022;61:e202203212. [PMID: 35357071 DOI: 10.1002/anie.202203212] [Cited by in Crossref: 1] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
6 Brześkiewicz J, Loska R. Palladium-Catalyzed Access to Benzocyclobutenone-Derived Ketonitrones via C(sp2)-H Functionalization. Org Lett 2022. [PMID: 35613705 DOI: 10.1021/acs.orglett.2c01317] [Reference Citation Analysis]
7 Lo C, Akula PS, Hong B, Lee G, Chien S. Total Synthesis of Ulodione A via a Double-Alkylation and DABCO Promoted Ring-Expansion Rearrangement Sequence. Org Lett . [DOI: 10.1021/acs.orglett.2c01038] [Cited by in Crossref: 2] [Article Influence: 2.0] [Reference Citation Analysis]
8 Wang YP, Fang K, Tu YQ, Yin JJ, Zhao Q, Ke T. An efficient approach to angular tricyclic molecular architecture via Nazarov-like cyclization and double ring-expansion cascade. Nat Commun 2022;13:2335. [PMID: 35484150 DOI: 10.1038/s41467-022-29947-5] [Reference Citation Analysis]
9 Xu JH, Liu ZK, Tang YL, Gao Y, Hu XQ. Merging strain-release and copper catalysis: the selective ring-opening cross-coupling of 1,2-oxazetidines with boronic acids. Chem Commun (Camb) 2022;58:4180-3. [PMID: 35266480 DOI: 10.1039/d2cc00461e] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
10 Ding L, Song H, Zheng C, You SL. Enantioselective Synthesis of Medium-Sized-Ring Lactones via Iridium-Catalyzed Z-Retentive Asymmetric Allylic Substitution Reaction. J Am Chem Soc 2022. [PMID: 35266702 DOI: 10.1021/jacs.2c01103] [Cited by in Crossref: 3] [Article Influence: 3.0] [Reference Citation Analysis]
11 Jia J, Yuan F, Zhang Z, Song X, Hu F, Xia Y. Copper-Catalyzed Ring-Opening Defluoroborylation of gem-Difluorinated Cyclobutenes: A General Route to Bifunctional 1,3-Dienes and Their Applications. Org Lett 2022. [PMID: 35238573 DOI: 10.1021/acs.orglett.2c00403] [Reference Citation Analysis]
12 Pati BV, Ghosh A, Yadav K, Banjare SK, Pandey S, Lourderaj U, Ravikumar PC. Palladium-catalyzed selective C-C bond cleavage and stereoselective alkenylation between cyclopropanol and 1,3-diyne: one-step synthesis of diverse conjugated enynes. Chem Sci 2022;13:2692-700. [PMID: 35340856 DOI: 10.1039/d1sc04780a] [Cited by in Crossref: 4] [Article Influence: 4.0] [Reference Citation Analysis]
13 Sindlinger M, Ströbele M, Maichle-Mössmer C, Bettinger HF. Kinetic stabilization allows structural analysis of a benzoborirene. Chem Commun (Camb) 2022;58:2818-21. [PMID: 35050291 DOI: 10.1039/d1cc06588b] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
14 Nishimoto M, Uetake Y, Yakiyama Y, Ishiwari F, Saeki A, Sakurai H. Synthesis of the C70 Fragment Buckybowl, Homosumanene, and Heterahomosumanenes via Ring-Expansion Reactions from Sumanenone. J Org Chem 2022. [PMID: 35179377 DOI: 10.1021/acs.joc.1c02416] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
15 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]
16 Xu Y, Zhai T, Xu Z, Ye L. Recent advances towards organocatalytic enantioselective desymmetrizing reactions. Trends in Chemistry 2022. [DOI: 10.1016/j.trechm.2021.12.010] [Cited by in Crossref: 2] [Article Influence: 2.0] [Reference Citation Analysis]
17 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]
18 Lepage RJ, Moore PW, Hewitt RJ, Teesdale-Spittle PH, Krenske EH, Harvey JE. Mechanistic Studies on the Base-Promoted Ring Opening of Glycal-Derived gem-Dibromocyclopropanes. J Org Chem 2021. [PMID: 34932347 DOI: 10.1021/acs.joc.1c02366] [Reference Citation Analysis]
19 Lee JY, Samala S, Kim J, Yoo EJ. Contractions of 1,4-Diazepines to Pyrroles Triggered by Valence Tautomerization: A One-Pot Approach and Mechanism. Org Lett 2021;23:9006-11. [PMID: 34752111 DOI: 10.1021/acs.orglett.1c03549] [Reference Citation Analysis]
20 Ning X, Chen Y, Hu F, Xia Y. Palladium-Catalyzed Carbene Coupling Reactions of Cyclobutanone N-Sulfonylhydrazones. Org Lett 2021;23:8348-52. [PMID: 34623163 DOI: 10.1021/acs.orglett.1c03052] [Reference Citation Analysis]