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 *

358 related articles for article (PubMed ID: 15575776)

  • 1. Highly efficient chemoselective deprotection of O,O-acetals and O,O-ketals catalyzed by molecular iodine in acetone.
    Sun J; Dong Y; Cao L; Wang X; Wang S; Hu Y
    J Org Chem; 2004 Dec; 69(25):8932-4. PubMed ID: 15575776
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Indium(III) trifluoromethanesulfonate as an efficient catalyst for the deprotection of acetals and ketals.
    Gregg BT; Golden KC; Quinn JF
    J Org Chem; 2007 Jul; 72(15):5890-3. PubMed ID: 17595139
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Unexpected highly chemoselective deprotection of the acetals from aldehydes and not ketones: TESOTf-2,6-lutidine combination.
    Fujioka H; Sawama Y; Murata N; Okitsu T; Kubo O; Matsuda S; Kita Y
    J Am Chem Soc; 2004 Sep; 126(38):11800-1. PubMed ID: 15382908
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Iron(III)-catalyzed cyclization of alkynyl aldehyde acetals: experimental and computational studies.
    Xu T; Yang Q; Li D; Dong J; Yu Z; Li Y
    Chemistry; 2010 Aug; 16(30):9264-72. PubMed ID: 20583061
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Zeolite catalyzed selective deprotection of di- and tri-O-isopropylidene sugar acetals.
    Bhaskar PM; Mathiselvam M; Loganathan D
    Carbohydr Res; 2008 Jul; 343(10-11):1801-7. PubMed ID: 18502410
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Tetrabutylammonium tribromide (TBATB): a mild and efficient catalyst for O-isopropylidenation of carbohydrates.
    Khan AT; Khan MM; Adhikary A
    Carbohydr Res; 2011 Apr; 346(5):673-7. PubMed ID: 21333273
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Highly efficient deprotection of aromatic acetals under neutral conditions using beta-cyclodextrin in water.
    Krishnaveni NS; Surendra K; Reddy MA; Nageswar YV; Rao KR
    J Org Chem; 2003 Mar; 68(5):2018-9. PubMed ID: 12608827
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Electrochemical Oxidative Decarboxylation of Malonic Acid Derivatives: A Method for the Synthesis of Ketals and Ketones.
    Ma X; Luo X; Dochain S; Mathot C; Markò IE
    Org Lett; 2015 Oct; 17(19):4690-3. PubMed ID: 26392322
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Unusual carbon-carbon bond formations between allylboronates and acetals or ketals catalyzed by a peculiar indium(I) Lewis acid.
    Schneider U; Dao HT; Kobayashi S
    Org Lett; 2010 Jun; 12(11):2488-91. PubMed ID: 20462242
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A simple and efficient chemoselective method for the catalytic deprotection of acetals and ketals using bismuth triflate.
    Carrigan MD; Sarapa D; Smith RC; Wieland LC; Mohan RS
    J Org Chem; 2002 Feb; 67(3):1027-30. PubMed ID: 11856058
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A mild deprotection of isopropylidene ketals from 2-deoxyglycosides using AcOH/H
    Ding XG; Zheng J; Cai XR; Su J; Wang Q; Wang YW; Liu XN; Liang XY
    Carbohydr Res; 2024 Jul; 541():109167. PubMed ID: 38823063
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Efficient synthesis of highly functionalized dihydropyrido[2,3-d]pyrimidines by a double annulation strategy from alpha-alkenoyl-alpha-carbamoyl ketene-(S,S)-acetals.
    Zhao L; Liang F; Bi X; Sun S; Liu Q
    J Org Chem; 2006 Feb; 71(3):1094-8. PubMed ID: 16438526
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The acid hydrolysis mechanism of acetals catalyzed by a supramolecular assembly in basic solution.
    Pluth MD; Bergman RG; Raymond KN
    J Org Chem; 2009 Jan; 74(1):58-63. PubMed ID: 19113901
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Highly efficient access to bi- and tricyclic ketals through gold-catalyzed tandem reactions of 4-acyl-1,6-diynes.
    Meng J; Zhao YL; Ren CQ; Li Y; Li Z; Liu Q
    Chemistry; 2009; 15(8):1830-4. PubMed ID: 19132708
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Organoiridium complexes: efficient catalysts for the formation of sugar acetals and ketals.
    Mandal S; Verma PR; Mukhopadhyay B; Gupta P
    Carbohydr Res; 2011 Sep; 346(13):2007-10. PubMed ID: 21632036
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Iodine-sodium cyanoborohydride-mediated reductive ring opening of 4,6-O-benzylidene acetals of hexopyranosides.
    Rao KV; Patil PR; Atmakuri S; Kartha KP
    Carbohydr Res; 2010 Dec; 345(18):2709-13. PubMed ID: 21055729
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Organic chemistry using weakly electrophilic salts: efficient formation of O,O-mixed, O,S- and N,O-acetals.
    Fujioka H; Okitsu T; Ohnaka T; Li R; Kubo O; Okamoto K; Sawama Y; Kita Y
    J Org Chem; 2007 Oct; 72(21):7898-902. PubMed ID: 17887700
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Reaction of the acetals with TESOTf-base combination; speculation of the intermediates and efficient mixed acetal formation.
    Fujioka H; Okitsu T; Sawama Y; Murata N; Li R; Kita Y
    J Am Chem Soc; 2006 May; 128(17):5930-8. PubMed ID: 16637661
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Lewis acid catalyzed reaction of arylvinylidenecyclopropanes with acetals: a facile synthetic protocol for the preparation of indene derivatives.
    Lu JM; Shi M
    Org Lett; 2006 Nov; 8(23):5317-20. PubMed ID: 17078707
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Lewis Acid Catalyzed Synthesis of α-Trifluoromethyl Esters and Lactones by Electrophilic Trifluoromethylation.
    Katayev D; Matoušek V; Koller R; Togni A
    Org Lett; 2015 Dec; 17(23):5898-901. PubMed ID: 26588788
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 18.