BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

125 related articles for article (PubMed ID: 37039446)

  • 1.
    Samudrala RP; Penjarla S; Penta S; Gundla R; Chandra Rao BP
    Nucleosides Nucleotides Nucleic Acids; 2023; 42(10):797-806. PubMed ID: 37039446
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Selective deprotection of terminal isopropylidene acetals and trityl ethers using HClO4 supported on silica gel.
    Agarwal A; Vankar YD
    Carbohydr Res; 2005 Jul; 340(9):1661-7. PubMed ID: 15890321
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. Selective cleavage of methoxy protecting groups in carbohydrates.
    Boto A; Hernández D; Hernández R; Suárez E
    J Org Chem; 2006 Mar; 71(5):1938-48. PubMed ID: 16496979
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Selective deprotection of 2',6'-di-O-benzyl-2,3:5,6:3',4'-tri-O-isopropylidenelactose dimethyl acetal.
    Catelani G; D'Andrea F; Puccioni L
    Carbohydr Res; 2000 Feb; 324(3):204-9. PubMed ID: 10724535
    [TBL] [Abstract][Full Text] [Related]  

  • 8. New protecting groups for 1,2-diols (boc- and moc-ethylidene). Cleavage of acetals with bases.
    Ariza X; Costa AM; Faja M; Pineda O; Vilarrasa J
    Org Lett; 2000 Sep; 2(18):2809-11. PubMed ID: 10964371
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Mild deprotection of methylene acetals in combination with trimethylsilyl triflate-2,2'-bipyridyl.
    Fujioka H; Senami K; Kubo O; Yahata K; Minamitsuji Y; Maegawa T
    Chem Pharm Bull (Tokyo); 2010 Mar; 58(3):426-8. PubMed ID: 20190457
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Photochemistry of 2-nitrobenzylidene acetals.
    Sebej P; Solomek T; Hroudná L; Brancová P; Klán P
    J Org Chem; 2009 Nov; 74(22):8647-58. PubMed ID: 19824651
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A reinvestigation of the synthesis and revision of spectral data of 1,2-O-isopropylidene-α-l-sorbofuranose, 1,2:4,6-di-O-isopropylidene-α-L-sorbofuranose and derivatives.
    Biela-Banaś A; Gallienne E; Martin OR
    Carbohydr Res; 2013 Oct; 380():23-8. PubMed ID: 23896160
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. An efficient synthesis of methyl 1,3-O-isopropylidene-alpha-D-fructofuranoside and 2,3:5,6-di-O-isopropylidene-D-glucose dimethyl acetal derivatives from sucrose.
    Hanaya T; Sato N; Yamamoto H
    Carbohydr Res; 2005 Nov; 340(16):2494-501. PubMed ID: 16168975
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Cyanomethyl (CNMe) ether: an orthogonal protecting group for saccharides.
    Molla MR; Thakur R
    Org Biomol Chem; 2022 May; 20(19):4030-4037. PubMed ID: 35506910
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Hafnium(IV) Chloride Catalyzes Highly Efficient Acetalization of Carbonyl Compounds.
    Bonilla-Landa I; López-Hernández E; Barrera-Méndez F; Salas NC; Olivares-Romero JL
    Curr Org Synth; 2019; 16(6):913-920. PubMed ID: 31984912
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Syntheses and reactions of 5-O-acetyl-1,2-anhydro-3-O-benzyl-alpha-D-ribofuranose and beta-D-lyxofuranose, 5-O-acetyl-1,2-anhydro-3,6-di-O-benzyl- and 1,2-anhydro-5,6-di-O-benzoyl-3-O-benzyl-beta-D-mannofuranose, and 6-O-acetyl-1,2-anhydro-3,4-di-O-benzyl-alpha-D-glucopyranose and -beta-D-talopyranose.
    Ning J; Kong F
    Carbohydr Res; 2001 Jan; 330(2):165-75. PubMed ID: 11217969
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Ni-catalyzed homoallylation of polyhydroxy n,o-acetals with conjugated dienes promoted by triethylborane.
    Mori T; Akioka Y; Onodera G; Kimura M
    Molecules; 2014 Jul; 19(7):9288-306. PubMed ID: 24991760
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Stripping off water at ambient temperature: direct atom-efficient acetal formation between aldehydes and diols catalyzed by water-tolerant and recoverable vanadyl triflate.
    Chen CT; Weng SS; Kao JQ; Lin CC; Jan MD
    Org Lett; 2005 Jul; 7(15):3343-6. PubMed ID: 16018656
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.