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 *

148 related articles for article (PubMed ID: 34374288)

  • 1. Stereoselective Installation of Five Contiguous Stereogenic Centers in a Double Aldol-Tishchenko Cascade and Evaluation of the Key Transition State through DFT Calculation.
    Mackey P; Turlik A; Ando K; Light ME; Houk KN; McGlacken GP
    Org Lett; 2021 Aug; 23(16):6372-6376. PubMed ID: 34374288
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Asymmetric Aldol-Tishchenko Reaction of Sulfinimines.
    Foley VM; McSweeney CM; Eccles KS; Lawrence SE; McGlacken GP
    Org Lett; 2015 Nov; 17(22):5642-5. PubMed ID: 26528888
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The Aldol-Tishchenko Reaction of Butanone, Cyclobutanone and a 3-Pentanone Derived Sulfinylimine and DFT Calculations of the Stereo-determining Step.
    Alcock E; Mackey P; Turlik A; Bhatt K; Light ME; Houk KN; McGlacken GP
    Chemistry; 2023 Apr; 29(22):e202203029. PubMed ID: 36617506
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Samarium Ion-Promoted Cross-Aldol Reactions and Tandem Aldol/Evans-Tishchenko Reactions.
    Lu L; Chang HY; Fang JM
    J Org Chem; 1999 Feb; 64(3):843-853. PubMed ID: 11674156
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Direct enantioselective aldol-Tishchenko reaction catalyzed by chiral lithium diphenylbinaphtholate.
    Ichibakase T; Nakajima M
    Org Lett; 2011 Apr; 13(7):1579-81. PubMed ID: 21355567
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Stereoselective Synthesis of 2-Fluoro-1,3-Diols via Lithium Binaphtholate-Catalyzed Aldol-Tishchenko Reaction.
    Asano T; Kotani S; Nakajima M
    Org Lett; 2019 Jun; 21(11):4192-4196. PubMed ID: 31120256
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mechanism and Origins of Stereoselectivity of the Aldol-Tishchenko Reaction of Sulfinimines.
    Turlik A; Ando K; Mackey P; Alcock E; Light M; McGlacken GP; Houk KN
    J Org Chem; 2021 Mar; 86(5):4296-4303. PubMed ID: 33586983
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Direct catalytic asymmetric aldol-Tishchenko reaction.
    Gnanadesikan V; Horiuchi Y; Ohshima T; Shibasaki M
    J Am Chem Soc; 2004 Jun; 126(25):7782-3. PubMed ID: 15212518
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Direct asymmetric aldol-Tishchenko reaction of aliphatic ketones catalyzed by syn-aminoalcohol-Yb(III) complexes.
    Mlynarski J; Jankowska J; Rakiel B
    Chem Commun (Camb); 2005 Oct; (38):4854-6. PubMed ID: 16193137
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Enantio- and Diastereoselective Two-Pot Synthesis of Isoquinuclidines from Glutaraldehyde and
    Ramaraju P; Pawar AP; Iype E; Mir NA; Choudhary S; Sharma DK; Kant R; Kumar I
    J Org Chem; 2019 Oct; 84(19):12408-12419. PubMed ID: 31486644
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Potassium Base-Promoted Diastereoselective Synthesis of 1,3-Diols from Allylic Alcohols and Aldehydes through a Tandem Allylic-Isomerization/Aldol-Tishchenko Reaction.
    Sai M
    Chem Asian J; 2021 Dec; 16(24):4053-4056. PubMed ID: 34651444
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Enantioselective Synthesis of Acyclic Stereotriads Featuring Fluorinated Tetrasubstituted Stereocenters.
    Shao N; Liu X; Monnier V; Charles L; Rodriguez J; Bressy C; Quintard A
    Chemistry; 2022 Jan; 28(5):e202103874. PubMed ID: 34821417
    [TBL] [Abstract][Full Text] [Related]  

  • 13. On the Mechanism of the Asymmetric Aldol Addition of Chiral N-Amino Cyclic Carbamate Hydrazones: Evidence of Non-Curtin-Hammett Behavior.
    Uddin MN; Knight JD; Rastelli EJ; Soubra-Ghaoui C; Albright TA; Wu CH; Wu JI; Coltart DM
    Chemistry; 2019 Dec; 25(70):16037-16047. PubMed ID: 31650641
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Merging α-Lithiation and Aldol-Tishchenko Reaction to Construct Polyols from Benzyl Ethers.
    Sedano C; Velasco R; Suárez-Pantiga S; Sanz R
    Org Lett; 2020 Oct; 22(20):8070-8075. PubMed ID: 32991180
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Highly diastereo- and enantioselective organocatalytic domino Michael/aldol reaction of acyclic 3-halogeno-1,2-diones to α,β-unsaturated aldehydes.
    Lefranc A; Guénée L; Alexakis A
    Org Lett; 2013 May; 15(9):2172-5. PubMed ID: 23607321
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Application of Polyamines and Amino Acid Derivatives Based on 2-Azabicycloalkane Backbone in Enantioselective Aldol Reaction.
    Iwan D; Kamińska K; Wojaczyńska E
    Molecules; 2021 Aug; 26(17):. PubMed ID: 34500600
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Diastereoselective aldol reaction of zincated 3-chloro-3-methyl-1-azaallylic anions as key step in the synthesis of 1,2,3,4-tetrasubstituted 3-chloroazetidines.
    Mangelinckx S; De Sterck B; Colpaert F; Catak S; Jacobs J; Rooryck S; Waroquier M; Van Speybroeck V; De Kimpe N
    J Org Chem; 2012 Apr; 77(7):3415-25. PubMed ID: 22390195
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Evans-Tishchenko coupling of heteroaryl aldehydes.
    Dorgan PD; Durrani J; Cases-Thomas MJ; Hulme AN
    J Org Chem; 2010 Nov; 75(21):7475-8. PubMed ID: 20929205
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Regulated-stereoselective construction of thirteen stereogenic centers necessary for the frame of (+)-discodermolide, based on iterative Lewis acid-promoted aldol reactions.
    Kiyooka S; Shahid KA; Goto F; Okazaki M; Shuto Y
    J Org Chem; 2003 Oct; 68(21):7967-78. PubMed ID: 14535772
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Organocatalytic Oxa-Michael/Michael/Michael/Aldol Condensation Quadruple Domino Sequence: Asymmetric Synthesis of Tricyclic Chromanes.
    Kumar M; Chauhan P; Bailey SJ; Jafari E; von Essen C; Rissanen K; Enders D
    Org Lett; 2018 Feb; 20(4):1232-1235. PubMed ID: 29406738
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.