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 *

158 related articles for article (PubMed ID: 35506910)

  • 1. 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]  

  • 2. Cyanomethyl Ether as an Orthogonal Participating Group for Stereoselective Synthesis of 1,2-
    Molla MR; Das P; Guleria K; Subramanian R; Kumar A; Thakur R
    J Org Chem; 2020 Aug; 85(15):9955-9968. PubMed ID: 32600042
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Synthesis of monophosphoryl lipid A using 2-naphtylmethyl ethers as permanent protecting groups.
    Verpalen ECJM; Brouwer AJ; Boons GJ
    Carbohydr Res; 2020 Dec; 498():108152. PubMed ID: 33032087
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Temporary ether protecting groups at the anomeric center in complex carbohydrate synthesis.
    Li W; Yu B
    Adv Carbohydr Chem Biochem; 2020; 77():1-69. PubMed ID: 33004110
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Lipase-Mediated Conversion of Protecting Group Silyl Ethers: An Unspecific Side Reaction.
    Pick LM; Wenzlaff J; Yousefi M; Davari MD; Ansorge-Schumacher MB
    Chembiochem; 2023 Sep; 24(18):e202300384. PubMed ID: 37224395
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Enhanced diastereoselectivity in beta-mannopyranosylation through the use of sterically minimal propargyl ether protecting groups.
    Crich D; Jayalath P; Hutton TK
    J Org Chem; 2006 Apr; 71(8):3064-70. PubMed ID: 16599600
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Asymmetric Total Synthesis of Brasiliquinones B and C via Oxidative Cyclization of a Hydroquinone-Silyl Enol Ether Hybrid.
    Miyake H; Nakajima R; Kumamoto T
    J Org Chem; 2022 Sep; 87(18):12491-12497. PubMed ID: 36042538
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Development of a photolabile carbonyl-protecting group toolbox.
    Yang H; Zhang X; Zhou L; Wang P
    J Org Chem; 2011 Apr; 76(7):2040-8. PubMed ID: 21370916
    [TBL] [Abstract][Full Text] [Related]  

  • 11. NFSI mediated C3-ether oxidation of glycals for the synthesis of hex-3-enuloses.
    Das P; Thakur R
    Carbohydr Res; 2024 Feb; 536():109032. PubMed ID: 38219634
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Studies on several reactions with alkyl vinyl ethers and their derivatives. V. Some reactions of acetals and ether-acetal compounds].
    KOBAYASHI E; YUSAWA A
    Yakugaku Zasshi; 1962 Mar; 82():451-2. PubMed ID: 14457434
    [No Abstract]   [Full Text] [Related]  

  • 13. Straightforward synthesis of protected 2-hydroxyglycals by chlorination-dehydrochlorination of carbohydrate hemiacetals.
    Choutka J; Kratochvíl M; Zýka J; Pohl R; Parkan K
    Carbohydr Res; 2020 Oct; 496():108086. PubMed ID: 32828008
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Systematic Study of Regioselective Reductive Ring-Opening Reactions of 4,6-
    Mezö E; Herczeg M; Demeter F; Bereczki I; Csávás M; Borbás A
    J Org Chem; 2021 Sep; 86(18):12973-12987. PubMed ID: 34478619
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Zinc triflate-benzoyl bromide: a versatile reagent for the conversion of ether into benzoate protecting groups and ether glycosides into glycosyl bromides.
    Polat T; Linhardt RJ
    Carbohydr Res; 2003 Feb; 338(5):447-9. PubMed ID: 12559747
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Synthesis of dialkyl ethers from organotrifluoroborates and acetals.
    Mitchell TA; Bode JW
    J Am Chem Soc; 2009 Dec; 131(50):18057-9. PubMed ID: 20000858
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Taming the Reactivity of Glycosyl Iodides To Achieve Stereoselective Glycosidation.
    Gervay-Hague J
    Acc Chem Res; 2016 Jan; 49(1):35-47. PubMed ID: 26524481
    [TBL] [Abstract][Full Text] [Related]  

  • 18. New strategies for protecting group chemistry: synthesis, reactivity, and indirect oxidative cleavage of para-siletanylbenzyl ethers.
    Tlais SF; Lam H; House SE; Dudley GB
    J Org Chem; 2009 Mar; 74(5):1876-85. PubMed ID: 19183037
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The dimethoxyphenylbenzyl protecting group: an alternative to the p-methoxybenzyl group for protection of carbohydrates.
    Rankin GM; Maxwell-Cameron I; Painter GF; Larsen DS
    J Org Chem; 2013 Jun; 78(11):5264-72. PubMed ID: 23678997
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Combinatorial synthesis of deoxyhexasaccharides related to the landomycin A sugar moiety, based on an orthogonal deprotection strategy.
    Tanaka H; Yamaguchi S; Yoshizawa A; Takagi M; Shin-ya K; Takahashi T
    Chem Asian J; 2010 Jun; 5(6):1407-24. PubMed ID: 20480491
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.