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For: Alves NG, Alves AJS, Soares MIL, Pinho e Melo TMVD. Recent Advances in the Synthesis of Spiro‐β‐Lactams and Spiro‐δ‐Lactams. Adv Synth Catal 2021;363:2464-501. [DOI: 10.1002/adsc.202100013] [Cited by in Crossref: 8] [Cited by in F6Publishing: 10] [Article Influence: 8.0] [Reference Citation Analysis]
Number Citing Articles
1 Alves AJS, Alves NG, Bártolo I, Fontinha D, Caetano S, Prudêncio M, Taveira N, Pinho e Melo TMVD. Unveiling a family of spiro-β-lactams with anti-HIV and antiplasmodial activity via phosphine-catalyzed [3+2] annulation of 6-alkylidene-penicillanates and allenoates. Front Chem 2022;10:1017250. [DOI: 10.3389/fchem.2022.1017250] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
2 Griffiths OM, Ley SV. Multicomponent Direct Assembly of N -Heterospirocycles Facilitated by Visible-Light-Driven Photocatalysis. J Org Chem . [DOI: 10.1021/acs.joc.2c01684] [Reference Citation Analysis]
3 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]
4 Alves AJS, Silvestre JAD, Pinho e Melo TMVD. Synthesis of novel chiral spiro-β-lactams from nitrile oxides and 6-(Z)-(benzoylmethylene)penicillanate: batch, microwave-induced and continuous flow methodologies. RSC Adv 2022;12:30879-30891. [DOI: 10.1039/d2ra04848e] [Reference Citation Analysis]
5 Abazid AH, Nachtsheim BJ. Application of chiral triazole-substituted iodoarenes in the enantioselective construction of spirooxazolines. Chem Commun (Camb) 2021;57:8822-5. [PMID: 34382967 DOI: 10.1039/d1cc03246a] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
6 Guin S, Majee D, Samanta S. Unmasking the reverse reactivity of cyclic N-sulfonyl ketimines: multifaceted applications in organic synthesis. Chem Commun (Camb) 2021;57:9010-28. [PMID: 34498642 DOI: 10.1039/d1cc03439a] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 5.0] [Reference Citation Analysis]