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For: Gregson CHU, Noble A, Aggarwal VK. Divergent, Strain-Release Reactions of Azabicyclo[1.1.0]butyl Carbinols: Semipinacol or Spiroepoxy Azetidine Formation. Angew Chem Int Ed Engl 2021;60:7360-5. [PMID: 33555105 DOI: 10.1002/anie.202100583] [Cited by in Crossref: 7] [Cited by in F6Publishing: 10] [Article Influence: 7.0] [Reference Citation Analysis]
Number Citing Articles
1 Musci P, Colella M, Andresini M, Aramini A, Degennaro L, Luisi R. Flow technology enabled preparation of C3-heterosubstituted 1-azabicyclo[1.1.0]butanes and azetidines: accessing unexplored chemical space in strained heterocyclic chemistry. Chem Commun (Camb) 2022;58:6356-9. [PMID: 35536561 DOI: 10.1039/d2cc01641a] [Reference Citation Analysis]
2 Rao MLN, Islam SS. Rearrangement-Driven Molecular Diversity: Synthesis of Functionalized Pyrones, Orthoesters, and Xanthones from Spiroketals. Org Lett 2021;23:8668-72. [PMID: 34714091 DOI: 10.1021/acs.orglett.1c02888] [Reference Citation Analysis]
3 Tyler JL, Noble A, Aggarwal VK. Strain-Release-Driven Friedel-Crafts Spirocyclization of Azabicyclo[1.1.0]butanes. Angew Chem Int Ed Engl 2021. [PMID: 34780681 DOI: 10.1002/anie.202114235] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
4 Colella M, Musci P, Cannillo D, Spennacchio M, Aramini A, Degennaro L, Luisi R. Development of a Continuous Flow Synthesis of 2-Substituted Azetines and 3-Substituted Azetidines by Using a Common Synthetic Precursor. J Org Chem 2021;86:13943-54. [PMID: 34291947 DOI: 10.1021/acs.joc.1c01297] [Reference Citation Analysis]
5 Pinkert T, Das M, Schrader ML, Glorius F. Use of Strain-Release for the Diastereoselective Construction of Quaternary Carbon Centers. J Am Chem Soc 2021;143:7648-54. [PMID: 33974436 DOI: 10.1021/jacs.1c03492] [Cited by in Crossref: 2] [Cited by in F6Publishing: 9] [Article Influence: 2.0] [Reference Citation Analysis]
6 Wierzba AJ, Gryko DT, Gryko D. Acylation of electrophilic bicyclo[1.1.0]butanes via Co/Ni-catalyzed reductive cross-coupling. J Porphyrins Phthalocyanines 2021;25:630-8. [DOI: 10.1142/s1088424621500528] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
7 Tyler JL, Noble A, Aggarwal VK. Strain-Release Driven Spirocyclization of Azabicyclo[1.1.0]butyl Ketones. Angew Chem Int Ed Engl 2021;60:11824-9. [PMID: 33754432 DOI: 10.1002/anie.202102754] [Cited by in Crossref: 1] [Cited by in F6Publishing: 4] [Article Influence: 1.0] [Reference Citation Analysis]
8 Kerner MJ, Wipf P. Semipinacol-Type Rearrangements of [3-(Arylsulfonyl)bicyclo[1.1.0]butan-1-yl]alkanols. Org Lett 2021;23:3615-9. [PMID: 33872016 DOI: 10.1021/acs.orglett.1c01004] [Cited by in Crossref: 2] [Cited by in F6Publishing: 5] [Article Influence: 2.0] [Reference Citation Analysis]
9 Tyler JL, Noble A, Aggarwal VK. Strain‐Release Driven Spirocyclization of Azabicyclo[1.1.0]butyl Ketones. Angew Chem 2021;133:11930-5. [DOI: 10.1002/ange.202102754] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
10 Gregson CHU, Noble A, Aggarwal VK. Divergent, Strain-Release Reactions of Azabicyclo[1.1.0]butyl Carbinols: Semipinacol or Spiroepoxy Azetidine Formation. Angew Chem Int Ed Engl 2021;60:7360-5. [PMID: 33555105 DOI: 10.1002/anie.202100583] [Cited by in Crossref: 7] [Cited by in F6Publishing: 10] [Article Influence: 7.0] [Reference Citation Analysis]