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For: Ma X, Pinto W, Pham LN, Sloman DL, Han Y. Synthetic Studies of 2,2-Difluorobicyclo[1.1.1]pentanes (BCP-F 2 ): The Scope and Limitation of Useful Building Blocks for Medicinal Chemists: Synthetic Studies of 2,2-Difluorobicyclo[1.1.1]pentanes (BCP-F 2 ): The Scope and Limitation of Useful Building Blocks for Medicinal Chemists. Eur J Org Chem 2020;2020:4581-605. [DOI: 10.1002/ejoc.202000679] [Cited by in Crossref: 6] [Cited by in F6Publishing: 10] [Article Influence: 3.0] [Reference Citation Analysis]
Number Citing Articles
1 Bychek R, Mykhailiuk PK. A Practical and Scalable Approach to Fluoro-Substituted Bicyclo[1.1.1]pentanes. Angew Chem Int Ed Engl 2022;61:e202205103. [PMID: 35638404 DOI: 10.1002/anie.202205103] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
2 Bychek R, Mykhailiuk PK. A Practical and Scalable Approach to Fluoro‐Substituted Bicyclo[1.1.1]pentanes. Angewandte Chemie. [DOI: 10.1002/ange.202205103] [Reference Citation Analysis]
3 Jung M, Lindsay VNG. One-Pot Synthesis of Strain-Release Reagents from Methyl Sulfones. J Am Chem Soc . [DOI: 10.1021/jacs.2c00923] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
4 Schwartz BD, Smyth AP, Nashar PE, Gardiner MG, Malins LR. Investigating Bicyclobutane-Triazolinedione Cycloadditions as a Tool for Peptide Modification. Org Lett 2022. [PMID: 35014844 DOI: 10.1021/acs.orglett.1c04071] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 4.0] [Reference Citation Analysis]
5 McNamee RE, Thompson AL, Anderson EA. Synthesis and Applications of Polysubstituted Bicyclo[1.1.0]butanes. J Am Chem Soc 2021;143:21246-51. [PMID: 34904841 DOI: 10.1021/jacs.1c11244] [Reference Citation Analysis]
6 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]
7 Ma X, Yeung CS. Achieving C(sp2)-C(sp3) Coupling with BCP-F2 Building Blocks via Barluenga Coupling: A Comparative Approach. J Org Chem 2021;86:10672-98. [PMID: 34314187 DOI: 10.1021/acs.joc.1c01370] [Reference Citation Analysis]
8 Le TP, Rončević I, Dračínský M, Císařová I, Šolínová V, Kašička V, Kaleta J. Polyhalogenated Bicyclo[1.1.1]pentane-1,3-dicarboxylic Acids. J Org Chem 2021;86:10303-19. [PMID: 34269057 DOI: 10.1021/acs.joc.1c01020] [Reference Citation Analysis]
9 Anderson JM, Measom ND, Murphy JA, Poole DL. Bridge Functionalisation of Bicyclo[1.1.1]pentane Derivatives. Angew Chem Int Ed Engl 2021. [PMID: 34151501 DOI: 10.1002/anie.202106352] [Cited by in F6Publishing: 8] [Reference Citation Analysis]
10 Ma X, Han Y, Bennett DJ. Selective Synthesis of 1-Dialkylamino-2-alkylbicyclo-[1.1.1]pentanes. Org Lett 2020;22:9133-8. [DOI: 10.1021/acs.orglett.0c03612] [Cited by in Crossref: 7] [Cited by in F6Publishing: 5] [Article Influence: 3.5] [Reference Citation Analysis]