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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

332 related articles for article (PubMed ID: 31609533)

  • 21. Spiroketal-based diphosphine ligands in Pd-catalyzed asymmetric allylic amination of Morita-Baylis-Hillman adducts: exceptionally high efficiency and new mechanism.
    Wang X; Guo P; Han Z; Wang X; Wang Z; Ding K
    J Am Chem Soc; 2014 Jan; 136(1):405-11. PubMed ID: 24328176
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Development of Synthetic Methodologies via Catalytic Enantioselective Synthesis of 3,3-Disubstituted Oxindoles.
    Cao ZY; Zhou F; Zhou J
    Acc Chem Res; 2018 Jun; 51(6):1443-1454. PubMed ID: 29808678
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Highly enantio- and diastereoselective allylic alkylation of Morita-Baylis-Hillman carbonates with allyl ketones.
    Tong G; Zhu B; Lee R; Yang W; Tan D; Yang C; Han Z; Yan L; Huang KW; Jiang Z
    J Org Chem; 2013 May; 78(10):5067-72. PubMed ID: 23594149
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Organocatalyzed Asymmetric Vinylogous Allylic-Allylic Alkylation of Morita-Baylis-Hillman Carbonates with Olefinic Azlactones: Facile Access to Chiral Multifunctional α-Amino Acid Derivatives.
    Zhao S; Zhao YY; Lin JB; Xie T; Liang YM; Xu PF
    Org Lett; 2015 Jul; 17(13):3206-9. PubMed ID: 26075590
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Tertiary amine-catalyzed chemoselective and asymmetric [3 + 2] annulation of Morita-Baylis-Hillman carbonates of isatins with propargyl sulfones.
    Peng J; Huang X; Jiang L; Cui HL; Chen YC
    Org Lett; 2011 Sep; 13(17):4584-7. PubMed ID: 21815615
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Organocatalytic Synthesis of Highly Functionalized Heterocycles by Enantioselective aza-Morita-Baylis-Hillman-Type Domino Reactions.
    Takizawa S
    Chem Pharm Bull (Tokyo); 2020; 68(4):299-315. PubMed ID: 32238648
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Aqueous Morita-Baylis-Hillman reaction of unprotected isatins with cyclic enones.
    Gomes JC; Sirvent J; Moyano A; Rodrigues MT; Coelho F
    Org Lett; 2013 Nov; 15(22):5838-41. PubMed ID: 24188034
    [TBL] [Abstract][Full Text] [Related]  

  • 28. (DHQ)2AQN-catalyzed asymmetric substitution of isatin-derived hydrazones with O-Boc-protected Morita-Baylis-Hillman adducts: A strategy for synthesizing enantioenriched azo compounds incorporating an oxindole scaffold.
    Yang HB; Zhao YZ; Sang R; Shi M
    J Org Chem; 2014 Apr; 79(8):3519-28. PubMed ID: 24670223
    [TBL] [Abstract][Full Text] [Related]  

  • 29. An enantioselective organocatalyzed aza-Morita-Baylis-Hillman reaction of isatin-derived ketimines with acrolein.
    Yoshida Y; Sako M; Kishi K; Sasai H; Hatakeyama S; Takizawa S
    Org Biomol Chem; 2015 Sep; 13(34):9022-8. PubMed ID: 26214279
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Recent advances in the annulation of Morita-Baylis-Hillman adducts.
    Zhong NJ; Wang YZ; Cheng L; Wang D; Liu L
    Org Biomol Chem; 2018 Jul; 16(29):5214-5227. PubMed ID: 29964282
    [TBL] [Abstract][Full Text] [Related]  

  • 31. One-pot tandem approach to spirocyclic oxindoles featuring adjacent spiro-stereocenters.
    Liu YL; Wang X; Zhao YL; Zhu F; Zeng XP; Chen L; Wang CH; Zhao XL; Zhou J
    Angew Chem Int Ed Engl; 2013 Dec; 52(51):13735-9. PubMed ID: 24346948
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Synthesis, biological activities, and structure-activity relationships of Morita-Baylis-Hillman adducts: An update.
    Devi N; Pathania AS; Singh V; Sharma S
    Arch Pharm (Weinheim); 2024 Oct; 357(10):e2400372. PubMed ID: 38963326
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Recent extensions of the Morita-Baylis-Hillman reaction.
    Ma GN; Jiang JJ; Shi M; Wei Y
    Chem Commun (Camb); 2009 Oct; (37):5496-514. PubMed ID: 19753340
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Enantioselective Morita-Baylis-Hillman reaction of isatins with acrylates: facile creation of 3-hydroxy-2-oxindoles.
    Zhong F; Chen GY; Lu Y
    Org Lett; 2011 Jan; 13(1):82-5. PubMed ID: 21138329
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Lewis Base-Catalyzed [4 + 3] Annulation of ortho-Quinone Methides and MBH Carbonates: Synthesis of Functionalized Benzo[ b]oxepines Bearing Oxindole Scaffolds.
    Du JY; Ma YH; Meng FX; Zhang RR; Wang RN; Shi HL; Wang Q; Fan YX; Huang HL; Cui JC; Ma CL
    Org Lett; 2019 Jan; 21(2):465-468. PubMed ID: 30618260
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Asymmetric (4 + 3) and (4 + 1) Annulations of Isatin-derived Morita-Baylis-Hillman Carbonates to Construct Diverse Chiral Heterocyclic Frameworks.
    Yan RJ; Liu BX; Xiao BX; Du W; Chen YC
    Org Lett; 2020 Jun; 22(11):4240-4244. PubMed ID: 32412770
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Chiral Phosphine Ligands of COAP and SKP Switched Regiodivergent Asymmetric Allylic Alkylation of MBH Adducts.
    Sun XY; Song JY; Wang BL; Zhou SS; Ou ZX; Li LB; Wang Z; Wang XW
    J Org Chem; 2024 Apr; 89(7):4904-4915. PubMed ID: 38500413
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Regio- and Enantioselective Allylic Amination of Aliphatic MBH Adducts with N-Heteroaromatics.
    Wang H; Yu L; Xie M; Wu J; Qu G; Ding K; Guo H
    Chemistry; 2018 Jan; 24(6):1425-1430. PubMed ID: 29125647
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Organocatalytic and electrophilic approach to oxindoles with C3-quaternary stereocenters.
    Peng J; Huang X; Cui HL; Chen YC
    Org Lett; 2010 Oct; 12(19):4260-3. PubMed ID: 20812696
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Recent advances in the synthetic applications of Morita-Baylis-Hillman and Rauhut-Currier adducts of nitroalkenes.
    Sivanandan ST; Nair DK; Namboothiri INN
    Org Biomol Chem; 2023 Aug; 21(31):6243-6262. PubMed ID: 37486601
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 17.