BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

185 related articles for article (PubMed ID: 25247255)

  • 21. Highly enantioselective asymmetric 1,3-dipolar cycloaddition of azomethine ylide catalyzed by a copper(I)/ClickFerrophos complex.
    Fukuzawa S; Oki H
    Org Lett; 2008 May; 10(9):1747-50. PubMed ID: 18373347
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Brucine diol-copper-catalyzed asymmetric synthesis of endo-pyrrolidines: the mechanistic dichotomy of imino esters.
    Li JY; Kim HY; Oh K
    Org Lett; 2015 Mar; 17(5):1288-91. PubMed ID: 25695534
    [TBL] [Abstract][Full Text] [Related]  

  • 23. A novel one-pot green synthesis of dispirooxindolo-pyrrolidines via 1,3-dipolar cycloaddition reactions of azomethine ylides.
    Almansour AI; Arumugam N; Kumar RS; Periyasami G; A Ghabbour H; Fun HK
    Molecules; 2015 Jan; 20(1):780-91. PubMed ID: 25574820
    [TBL] [Abstract][Full Text] [Related]  

  • 24. C-H functionalization of cyclic amines: redox-annulations with α,β-unsaturated carbonyl compounds.
    Kang Y; Richers MT; Sawicki CH; Seidel D
    Chem Commun (Camb); 2015 Jul; 51(53):10648-51. PubMed ID: 26051897
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Catalytic enantioselective 1,3-dipolar cycloaddition reaction of azomethine ylides and alkenes: the direct strategy to prepare enantioenriched highly substituted proline derivatives.
    Nájera C; Sansano JM
    Angew Chem Int Ed Engl; 2005 Oct; 44(39):6272-6. PubMed ID: 16172996
    [No Abstract]   [Full Text] [Related]  

  • 26. Synthesis of fluorous and nonfluorous polycyclic systems by one-pot, double intramolecular 1,3-dipolar cycloaddition of azomethine ylides.
    Zhang W; Lu Y; Geib S
    Org Lett; 2005 May; 7(11):2269-72. PubMed ID: 15901186
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Enantiospecific synthesis of the bridged pyrrolizidine core of asparagamine A: dipolar cycloadditions of azomethine ylides derived from the sulfonylation of vinylogous amides.
    Epperson MT; Gin DY
    Angew Chem Int Ed Engl; 2002 May; 41(10):1778-80. PubMed ID: 19750714
    [No Abstract]   [Full Text] [Related]  

  • 28. Synthesis of pyrrolo(spiro-[2.3']-oxindole)-spiro-[4.3"]-oxindole via 1,3-dipolar cycloaddition of azomethine ylides with 3-acetonylideneoxindole.
    Xiao JA; Zhang HG; Liang S; Ren JW; Yang H; Chen XQ
    J Org Chem; 2013 Nov; 78(22):11577-83. PubMed ID: 24111532
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Cascade condensation, cyclization, intermolecular dipolar cycloaddition by multi-component coupling and application to a synthesis of (+/-)-crispine A.
    Coldham I; Jana S; Watson L; Martin NG
    Org Biomol Chem; 2009 Apr; 7(8):1674-9. PubMed ID: 19343256
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Enantioselective synthesis of 4-aminopyrrolidine-2,4-dicarboxylate derivatives via Ag-catalyzed cycloaddition of azomethine ylides with alkylidene azlactones.
    González-Esguevillas M; Adrio J; Carretero JC
    Chem Commun (Camb); 2013 May; 49(41):4649-51. PubMed ID: 23579920
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Binaphthol-derived bisphosphoric acids serve as efficient organocatalysts for highly enantioselective 1,3-dipolar cycloaddition of azomethine ylides to electron-deficient olefins.
    He L; Chen XH; Wang DN; Luo SW; Zhang WQ; Yu J; Ren L; Gong LZ
    J Am Chem Soc; 2011 Aug; 133(34):13504-18. PubMed ID: 21780781
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Amine-catalyzed enantioselective 1,3-dipolar cycloadditions of aldehydes to C,N-cyclic azomethine imines.
    Li W; Jia Q; Du Z; Zhang K; Wang J
    Chemistry; 2014 Apr; 20(16):4559-62. PubMed ID: 24644273
    [TBL] [Abstract][Full Text] [Related]  

  • 33. The discovery of oxazolones-grafted spirooxindoles via three-component diversity oriented synthesis and their preliminary biological evaluation.
    Dong H; Song S; Li J; Xu C; Zhang H; Ouyang L
    Bioorg Med Chem Lett; 2015 Sep; 25(17):3585-91. PubMed ID: 26159483
    [TBL] [Abstract][Full Text] [Related]  

  • 34. An exo- and enantioselective 1,3-dipolar cycloaddition of azomethine ylides with alkylidene malonates catalyzed by a N,O-ligand/Cu(OAc)2-derived chiral complex.
    Wang M; Wang Z; Shi YH; Shi XX; Fossey JS; Deng WP
    Angew Chem Int Ed Engl; 2011 May; 50(21):4897-900. PubMed ID: 21538735
    [No Abstract]   [Full Text] [Related]  

  • 35. One-Pot Synthesis of Triazolobenzodiazepines Through Decarboxylative [3 + 2] Cycloaddition of Nonstabilized Azomethine Ylides and Cu-Free Click Reactions.
    Ma X; Zhang X; Qiu W; Zhang W; Wan B; Evans J; Zhang W
    Molecules; 2019 Feb; 24(3):. PubMed ID: 30743991
    [TBL] [Abstract][Full Text] [Related]  

  • 36. The copper-catalyzed asymmetric construction of a dispiropyrrolidine skeleton via 1,3-dipolar cycloaddition of azomethine ylides to α-alkylidene succinimides.
    Yang WL; Liu YZ; Luo S; Yu X; Fossey JS; Deng WP
    Chem Commun (Camb); 2015 Jun; 51(44):9212-5. PubMed ID: 25952504
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Asymmetric construction of 3-vinylidene-pyrrolidine derivatives containing allene moiety via Ag(I)/TF-BiphamPhos-catalyzed 1,3-dipolar cycloaddition of azomethine ylides with diethyl 2-(3,3-diphenylpropa-1,2-dienylidene) malonate.
    Xue ZY; Fang X; Wang CJ
    Org Biomol Chem; 2011 May; 9(10):3622-4. PubMed ID: 21472159
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Total Synthesis of Proposed Structure of Yuremamine and All Diastereomers Using [3+2]-Cycloaddition of Platinum-Containing Azomethine Ylide.
    Ohyama T; Uchida M; Kusama H; Iwasawa N
    Chem Asian J; 2015 Sep; 10(9):1850-3. PubMed ID: 26103522
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Alternating asymmetric self-induction in functionalized pyrrolidine oligomers.
    Kudryavtsev KV; Ivantcova PM; Churakov AV; Wiedmann S; Luy B; Muhle-Goll C; Zefirov NS; Bräse S
    Angew Chem Int Ed Engl; 2013 Nov; 52(48):12736-40. PubMed ID: 24123659
    [No Abstract]   [Full Text] [Related]  

  • 40. 1,3-dipolar cycloadditions from tricyclic hemiaminals. Synthesis of the quinocarcin core through catalyst-free generation of azomethine ylides.
    Huck L; González JF; de la Cuesta E; Menéndez JC; Avendaño C
    Org Biomol Chem; 2011 Sep; 9(18):6271-7. PubMed ID: 21773620
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.