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Journal Abstract Search

206 related items for PubMed ID: 20000488

  • 1. Aryl sulfoxides from allyl sulfoxides via [2,3]-sigmatropic rearrangement and domino Pd-catalyzed generation/arylation of sulfenate anions.
    Bernoud E, Le Duc G, Bantreil X, Prestat G, Madec D, Poli G.
    Org Lett; 2010 Jan 15; 12(2):320-3. PubMed ID: 20000488
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  • 5. Preparation of allyl sulfoxides by palladium-catalyzed allylic alkylation of sulfenate anions.
    Maitro G, Prestat G, Madec D, Poli G.
    J Org Chem; 2006 Sep 15; 71(19):7449-54. PubMed ID: 16958541
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  • 6. Palladium-Catalyzed Arylation of Aryl Sulfenate Anions with Aryl Bromides under Mild Conditions: Synthesis of Diaryl Sulfoxides.
    Jiang H, Jia T, Zhang M, Walsh PJ.
    Org Lett; 2016 Mar 04; 18(5):972-5. PubMed ID: 26878149
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  • 7. Palladium-Catalyzed Enantioselective Arylation of Aryl Sulfenate Anions: A Combined Experimental and Computational Study.
    Jia T, Zhang M, McCollom SP, Bellomo A, Montel S, Mao J, Dreher SD, Welch CJ, Regalado EL, Williamson RT, Manor BC, Tomson NC, Walsh PJ.
    J Am Chem Soc; 2017 Jun 21; 139(24):8337-8345. PubMed ID: 28537724
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  • 9. Palladium catalyzed diaryl sulfoxide generation from aryl benzyl sulfoxides and aryl chlorides.
    Jia T, Zhang M, Sagamanova IK, Wang CY, Walsh PJ.
    Org Lett; 2015 Mar 06; 17(5):1168-71. PubMed ID: 25686150
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  • 10. New three-step domino reaction, "thiophilic addition-beta-elimination of fluoride-[3,3] sigmatropic rearrangement": Synthesis of alpha-allylic and alpha,alpha-bis(allylic) alpha-trifluoromethyl dithioesters.
    Grellepois F, Timoshenko VM, Shermolovich YG, Portella C.
    Org Lett; 2006 Sep 14; 8(19):4323-6. PubMed ID: 16956217
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  • 11. A new class of organocatalysts: sulfenate anions.
    Zhang M, Jia T, Yin H, Carroll PJ, Schelter EJ, Walsh PJ.
    Angew Chem Int Ed Engl; 2014 Sep 26; 53(40):10755-8. PubMed ID: 25111259
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  • 12. Tertiary thiols from allylic thiocarbamates by tandem enantioselective [3,3]-sigmatropic rearrangement and stereospecific arylation.
    Mingat G, MacLellan P, Laars M, Clayden J.
    Org Lett; 2014 Feb 21; 16(4):1252-5. PubMed ID: 24502387
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  • 13. From Allylic Sulfoxides to Allylic Sulfenates: Fifty Years of a Never-Ending [2,3]-Sigmatropic Rearrangement.
    Colomer I, Velado M, Fernández de la Pradilla R, Viso A.
    Chem Rev; 2017 Dec 27; 117(24):14201-14243. PubMed ID: 29185726
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  • 15. Palladium-Catalyzed Enantioselective Alkenylation of Sulfenate Anions.
    Wu C, Berritt S, Liang X, Walsh PJ.
    Org Lett; 2019 Feb 15; 21(4):960-964. PubMed ID: 30694063
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  • 16. Pd-catalyzed sulfinylzincation of activated alkynes with 1-alkynyl sulfoxides as a sulfinyl source.
    Maezaki N, Yagi S, Yoshigami R, Maeda J, Suzuki T, Ohsawa S, Tsukamoto K, Tanaka T.
    J Org Chem; 2003 Jul 11; 68(14):5550-8. PubMed ID: 12839446
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  • 17. Remarkably mild and simple preparation of sulfenate anions from beta-sulfinylesters: a new route to enantioenriched sulfoxides.
    Caupène C, Boudou C, Perrio S, Metzner P.
    J Org Chem; 2005 Apr 01; 70(7):2812-5. PubMed ID: 15787576
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  • 18. Sequential hydrocarbon functionalization: allylic C-H oxidation/vinylic C-H arylation.
    Delcamp JH, White MC.
    J Am Chem Soc; 2006 Nov 29; 128(47):15076-7. PubMed ID: 17117844
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  • 19. Entering the leinamycin rearrangement via 2-(trimethylsilyl)ethyl sulfoxides.
    Keerthi K, Gates KS.
    Org Biomol Chem; 2007 May 21; 5(10):1595-600. PubMed ID: 17571189
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  • 20. Palladium/PC-Phos-Catalyzed Enantioselective Arylation of General Sulfenate Anions: Scope and Synthetic Applications.
    Wang L, Chen M, Zhang P, Li W, Zhang J.
    J Am Chem Soc; 2018 Mar 07; 140(9):3467-3473. PubMed ID: 29420023
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