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For: Mishra UK, Patel K, Ramasastry SSV. Synthesis of Cyclopropanoids via Substrate-Based Cyclization Pathways. Org Lett 2019;21:175-9. [PMID: 30543443 DOI: 10.1021/acs.orglett.8b03537] [Cited by in Crossref: 10] [Cited by in F6Publishing: 7] [Article Influence: 3.3] [Reference Citation Analysis]
Number Citing Articles
1 Liu D, Liu X, Sun J, Han Y, Yan CG. Domino reaction of bindone and 1,3-dipolarophiles for the synthesis of diverse spiro and fused indeno[1,2-a]fluorene-7,12-diones. Org Biomol Chem 2022;20:4964-9. [PMID: 35660847 DOI: 10.1039/d2ob00815g] [Reference Citation Analysis]
2 Deng R, Wu S, Mou C, Liu J, Zheng P, Zhang X, Chi YR. Carbene-Catalyzed Enantioselective Sulfonylation of Enone Aryl Aldehydes: A New Mode of Breslow Intermediate Oxidation. J Am Chem Soc 2022. [PMID: 35274946 DOI: 10.1021/jacs.1c13384] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
3 Fadeev AA, Makarov AS, Ivanova OA, Uchuskin MG, Trushkov IV. Extended Corey–Chaykovsky reactions: transformation of 2-hydroxychalcones to benzannulated 2,8-dioxabicyclo[3.2.1]octanes and 2,3-dihydrobenzofurans. Org Chem Front 2022;9:737-44. [DOI: 10.1039/d1qo01646f] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
4 Liu D, Liu X, Sun J, Yan CG. Selective Synthesis of Diverse Spiro-oxindole-fluorene Derivatives via a DABCO-Promoted Annulation Reaction of Bindone and 3-Methyleneoxindoles. J Org Chem 2021;86:14705-19. [PMID: 34661401 DOI: 10.1021/acs.joc.1c01513] [Reference Citation Analysis]
5 Ma SS, Jiang BL, Yu ZK, Zhang SJ, Xu BH. Cobalt-Catalyzed Chemoselective Transfer Hydrogenative Cyclization Cascade of Enone-Tethered Aldehydes. Org Lett 2021;23:3873-8. [PMID: 33960792 DOI: 10.1021/acs.orglett.1c00992] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
6 Denisa Bisag G, Ruggieri S, Fochi M, Bernardi L. Catalyst‐ and Substrate‐Dependent Chemodivergent Reactivity of Stabilised Sulfur Ylides with Salicylaldehydes. Adv Synth Catal 2021;363:3053-9. [DOI: 10.1002/adsc.202100124] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
7 Maurya JP, Ramasastry SSV. Divergent Michael/Aldol Cascades Under Semi-Aqueous Conditions: Synthesis of Cyclopenta- and Cycloheptannulated (Hetero)arenes. J Org Chem 2021;86:525-37. [PMID: 33395742 DOI: 10.1021/acs.joc.0c02195] [Cited by in Crossref: 2] [Article Influence: 2.0] [Reference Citation Analysis]
8 Singh B, Bankar SK, Kumar K, Ramasastry SSV. Palladium-catalysed 5-endo-trig allylic (hetero)arylation. Chem Sci 2020;11:4948-53. [PMID: 34122951 DOI: 10.1039/d0sc01932a] [Cited by in Crossref: 9] [Cited by in F6Publishing: 1] [Article Influence: 4.5] [Reference Citation Analysis]
9 Mishra UK, Patel K, Ramasastry SSV. Ring-Opening/Recyclization Cascades of Monoactivated Cyclopropanes. Org Lett 2020;22:3815-9. [PMID: 32330047 DOI: 10.1021/acs.orglett.0c01056] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
10 Bisag GD, Ruggieri S, Fochi M, Bernardi L. Sulfoxonium ylides: simple compounds with chameleonic reactivity. Org Biomol Chem 2020;18:8793-809. [DOI: 10.1039/d0ob01822h] [Cited by in Crossref: 17] [Article Influence: 8.5] [Reference Citation Analysis]
11 Song R, Yu H, Huang H, Chen Y. Controlled One‐Pot Synthesis of Multiple Heterocyclic Scaffolds Based on an Amphiphilic Claisen‐Schmidt Reaction Intermediate. ChemistrySelect 2019;4:14021-6. [DOI: 10.1002/slct.201904110] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
12 Patel K, Mishra UK, Mukhopadhyay D, Ramasastry SSV. Beyond the Corey-Chaykovsky Reaction: Synthesis of Unusual Cyclopropanoids via Desymmetrization and Thereof. Chem Asian J 2019;14:4568-71. [PMID: 31513351 DOI: 10.1002/asia.201901108] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 1.3] [Reference Citation Analysis]
13 Cao J, Sun J, Yan C. Construction of indeno[1,2- a ]fluorene via domino reaction of 1,3-indanedione and 3-arylideneindolin-2-ones or chalcones. Org Biomol Chem 2019;17:9008-13. [DOI: 10.1039/c9ob01779h] [Cited by in Crossref: 3] [Article Influence: 1.0] [Reference Citation Analysis]