These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
123 related articles for article (PubMed ID: 37695257)
1. Stereoselective Synthesis of Secondary and Tertiary Boronic Esters via Matteson Homologation. Tost M; Kazmaier U Org Lett; 2023 Sep; 25(37):6835-6839. PubMed ID: 37695257 [TBL] [Abstract][Full Text] [Related]
2. A Straightforward Synthesis of Polyketides via Ester Dienolate Matteson Homologation. Andler O; Kazmaier U Chemistry; 2021 Jan; 27(3):949-953. PubMed ID: 33089903 [TBL] [Abstract][Full Text] [Related]
3. Stereoselective Synthesis of Highly Substituted O-Heterocycles via Matteson Homologation: A Ring-Closing Metathesis Approach. Kinsinger T; Schäfer P; Kazmaier U Org Lett; 2023 May; 25(18):3303-3307. PubMed ID: 37102993 [TBL] [Abstract][Full Text] [Related]
4. Application of Vinyl Nucleophiles in Matteson Homologations. Kinsinger T; Kazmaier U Org Lett; 2022 May; 24(20):3599-3603. PubMed ID: 35583355 [TBL] [Abstract][Full Text] [Related]
5. Stereoselective Synthesis of a Protected Side Chain of Callipeltin A. Horn A; Kazmaier U Org Lett; 2022 Oct; 24(39):7072-7076. PubMed ID: 36149738 [TBL] [Abstract][Full Text] [Related]
6. Lithiation-borylation methodology and its application in synthesis. Leonori D; Aggarwal VK Acc Chem Res; 2014 Oct; 47(10):3174-83. PubMed ID: 25262745 [TBL] [Abstract][Full Text] [Related]
7. α-Sulfinyl Benzoates as Precursors to Li and Mg Carbenoids for the Stereoselective Iterative Homologation of Boronic Esters. Casoni G; Kucukdisli M; Fordham JM; Burns M; Myers EL; Aggarwal VK J Am Chem Soc; 2017 Aug; 139(34):11877-11886. PubMed ID: 28812893 [TBL] [Abstract][Full Text] [Related]
8. Stereoselective Synthesis of a Protected Side Chain of Meliponamycin A. Andler O; Kazmaier U Org Lett; 2022 Apr; 24(13):2541-2545. PubMed ID: 35343704 [TBL] [Abstract][Full Text] [Related]
9. Matteson Homologation-Based Total Synthesis of Lagunamide A. Gorges J; Kazmaier U Org Lett; 2018 Apr; 20(7):2033-2036. PubMed ID: 29578725 [TBL] [Abstract][Full Text] [Related]
10. Application of Allylzinc Reagents as Nucleophiles in Matteson Homologations. Andler O; Kazmaier U Org Lett; 2021 Nov; 23(21):8439-8444. PubMed ID: 34633200 [TBL] [Abstract][Full Text] [Related]
11. Aza-Matteson Reactions via Controlled Mono- and Double-Methylene Insertions into Nitrogen-Boron Bonds. Xie Q; Dong G J Am Chem Soc; 2021 Sep; 143(36):14422-14427. PubMed ID: 34491049 [TBL] [Abstract][Full Text] [Related]
12. Short Enantioselective Total Synthesis of Tatanan A and 3-epi-Tatanan A Using Assembly-Line Synthesis. Noble A; Roesner S; Aggarwal VK Angew Chem Int Ed Engl; 2016 Dec; 55(51):15920-15924. PubMed ID: 27865037 [TBL] [Abstract][Full Text] [Related]
13. Strain-Release-Driven Homologation of Boronic Esters: Application to the Modular Synthesis of Azetidines. Fawcett A; Murtaza A; Gregson CHU; Aggarwal VK J Am Chem Soc; 2019 Mar; 141(11):4573-4578. PubMed ID: 30836746 [TBL] [Abstract][Full Text] [Related]
14. Asymmetric Catalytic Hydroboration of Enol Carbamates Enables an Enantioselective Matteson Homologation. Kuznetsov DM; Ready JM Synlett; 2023 Nov; 34(18):2181-2186. PubMed ID: 39092078 [TBL] [Abstract][Full Text] [Related]
15. Vinylidene Homologation of Boronic Esters and its Application to the Synthesis of the Proposed Structure of Machillene. Fordham JM; Grayson MN; Aggarwal VK Angew Chem Int Ed Engl; 2019 Oct; 58(43):15268-15272. PubMed ID: 31365776 [TBL] [Abstract][Full Text] [Related]
16. Facile formation of β-hydroxyboronate esters by a Cu-catalyzed diboration/Matteson homologation sequence. Moore CM; Medina CR; Cannamela PC; McIntosh ML; Ferber CJ; Roering AJ; Clark TB Org Lett; 2014 Dec; 16(23):6056-9. PubMed ID: 25412356 [TBL] [Abstract][Full Text] [Related]
17. Homologation and alkylation of boronic esters and boranes by 1,2-metallate rearrangement of boronate complexes. Thomas SP; French RM; Jheengut V; Aggarwal VK Chem Rec; 2009; 9(1):24-39. PubMed ID: 19243084 [TBL] [Abstract][Full Text] [Related]