BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

153 related articles for article (PubMed ID: 25679053)

  • 1. Acid catalyzed alcoholysis of sulfinamides: unusual stereochemistry, kinetics and a question of mechanism involving sulfurane intermediates and their pseudorotation.
    Bujnicki B; Drabowicz J; Mikołajczyk M
    Molecules; 2015 Feb; 20(2):2949-72. PubMed ID: 25679053
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Nucleophilic Substitution at Tricoordinate Sulfur-Alkaline Hydrolysis of Optically Active Dialkoxysulfonium Salts: Stereochemistry, Mechanism and Reaction Energetics.
    Mikołajczyk M; Bujnicki B; Drabowicz J; Cypryk M
    Molecules; 2022 Nov; 27(23):. PubMed ID: 36500306
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Formation of cyclic sulfinates and sulfinamides through homolytic substitution at the sulfur atom.
    Coulomb J; Certal V; Fensterbank L; Lacôte E; Malacria M
    Angew Chem Int Ed Engl; 2006 Jan; 45(4):633-7. PubMed ID: 16365844
    [No Abstract]   [Full Text] [Related]  

  • 4. A stereospecific synthesis of chiral cyclic sulfinamides.
    Harmata M; Zheng P
    Org Lett; 2007 Dec; 9(25):5251-3. PubMed ID: 17990893
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Expedient synthesis of sulfinamides from sulfonyl chlorides.
    Harmata M; Zheng P; Huang C; Gomes MG; Ying W; Rayanil KO; Balan G; Calkins NL
    J Org Chem; 2007 Jan; 72(2):683-5. PubMed ID: 17221999
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Squaramide-tertiary amine catalyzed asymmetric cascade sulfa-Michael/Michael addition via dynamic kinetic resolution: access to highly functionalized chromans with three contiguous stereocenters.
    Yang W; Yang Y; Du DM
    Org Lett; 2013 Mar; 15(6):1190-3. PubMed ID: 23463941
    [TBL] [Abstract][Full Text] [Related]  

  • 7. An approach to the stereoselective synthesis of syn- and anti-1,3-diol derivatives. Retention of configuration in the Mitsunobu reaction.
    Ahn C; DeShong P
    J Org Chem; 2002 Mar; 67(6):1754-9. PubMed ID: 11895389
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Diversity-oriented asymmetric catalysis (DOAC): stereochemically divergent synthesis of thiochromanes using an imidazoline-aminophenol-nickel-catalyzed Michael/Henry reaction.
    Arai T; Yamamoto Y
    Org Lett; 2014 Mar; 16(6):1700-3. PubMed ID: 24601640
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Highly selective palladium catalyzed kinetic resolution and enantioselective substitution of racemic allylic carbonates with sulfur nucleophiles: asymmetric synthesis of allylic sulfides, allylic sulfones, and allylic alcohols.
    Gais HJ; Jagusch T; Spalthoff N; Gerhards F; Frank M; Raabe G
    Chemistry; 2003 Sep; 9(17):4202-21. PubMed ID: 12953206
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Highly stereoselective benzylation of N-sulfinylketimines.
    García Ruano JL; Alemán J; Parra A
    J Am Chem Soc; 2005 Sep; 127(37):13048-54. PubMed ID: 16159300
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Nucleophilic Substitution at Heteroatoms-Identity Substitution Reactions at Phosphorus and Sulfur Centers: Do They Proceed in a Concerted (S
    Mikołajczyk M; Cypryk M; Gostyński B; Kowalczewski J
    Molecules; 2022 Jan; 27(3):. PubMed ID: 35163860
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A Cation-Directed Enantioselective Sulfur-Mediated Michael/Mannich Three-Component Domino Reaction involving Chalcones as Michael Acceptors.
    Ding R; Zheng B; Wang Y; Peng Y
    Org Lett; 2015 Sep; 17(17):4128-31. PubMed ID: 26295594
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mechanistic studies on the Cu-catalyzed three-component reactions of sulfonyl azides, 1-alkynes and amines, alcohols, or water: dichotomy via a common pathway.
    Yoo EJ; Ahlquist M; Bae I; Sharpless KB; Fokin VV; Chang S
    J Org Chem; 2008 Jul; 73(14):5520-8. PubMed ID: 18557650
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Impregnated ruthenium on magnetite as a recyclable catalyst for the N-alkylation of amines, sulfonamides, sulfinamides, and nitroarenes using alcohols as electrophiles by a hydrogen autotransfer process.
    Cano R; Ramón DJ; Yus M
    J Org Chem; 2011 Jul; 76(14):5547-57. PubMed ID: 21615080
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Stereoinversion of tertiary alcohols to tertiary-alkyl isonitriles and amines.
    Pronin SV; Reiher CA; Shenvi RA
    Nature; 2013 Sep; 501(7466):195-9. PubMed ID: 24025839
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Chiral sulfur derivatives in the allylation of acyl hydrazones: C(2)-symmetric bis-sulfinamides as enhanced chiral organic promoters.
    Fernández I; Alcudia A; Gori B; Valdivia V; Recio R; García MV; Khiar N
    Org Biomol Chem; 2010 Oct; 8(19):4388-93. PubMed ID: 20694222
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The diastereoselective synthesis of quaternary substituted thioindolines from sulfur ylide intermediates.
    Nyong AM; Rainier JD
    J Org Chem; 2005 Jan; 70(2):746-8. PubMed ID: 15651836
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Rhodium-Catalyzed Synthesis of Organosulfur Compounds Involving S-S Bond Cleavage of Disulfides and Sulfur.
    Arisawa M; Yamaguchi M
    Molecules; 2020 Aug; 25(16):. PubMed ID: 32784672
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Palladium-catalyzed stereospecific substitution of alpha,beta-unsaturated gamma,delta-epoxy esters by alcohols with double inversion of configuration: synthesis of 4-alkoxy-5-hydroxy-2-pentenoates.
    Yu XQ; Yoshimura F; Ito F; Sasaki M; Hirai A; Tanino K; Miyashita M
    Angew Chem Int Ed Engl; 2008; 47(4):750-4. PubMed ID: 18069707
    [No Abstract]   [Full Text] [Related]  

  • 20. Development of asymmetric reactions catalyzed by chiral organotin-alkoxide reagents.
    Yanagisawa A; Yoshida K
    Chem Rec; 2013 Feb; 13(1):117-27. PubMed ID: 23424074
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.