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Journal Abstract Search

481 related items for PubMed ID: 16898811

  • 1. trans-hydroalumination/alkylation: one-pot synthesis of trisubstituted allylic alcohols.
    Langille NF, Jamison TF.
    Org Lett; 2006 Aug 17; 8(17):3761-4. PubMed ID: 16898811
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  • 5. Access to macrocyclic endocyclic and exocyclic allylic alcohols by nickel-catalyzed reductive cyclization of ynals.
    Knapp-Reed B, Mahandru GM, Montgomery J.
    J Am Chem Soc; 2005 Sep 28; 127(38):13156-7. PubMed ID: 16173738
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  • 6. Controllable stereoselective synthesis of trisubstituted alkenes by a catalytic three-component reaction of terminal alkynes, benzylic alcohols, and simple arenes.
    Li HH, Jin YH, Wang JQ, Tian SK.
    Org Biomol Chem; 2009 Aug 21; 7(16):3219-21. PubMed ID: 19641777
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  • 7. Addition of arylboronic acids to arylpropargyl alcohols en route to indenes and quinolines.
    Panteleev J, Huang RY, Lui EK, Lautens M.
    Org Lett; 2011 Oct 07; 13(19):5314-7. PubMed ID: 21916430
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  • 9. Aluminum-catalyzed asymmetric alkylations of pyridyl-substituted alkynyl ketones with dialkylzinc reagents.
    Friel DK, Snapper ML, Hoveyda AH.
    J Am Chem Soc; 2008 Jul 30; 130(30):9942-51. PubMed ID: 18588297
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  • 10. Synthesis of azide-alkyne fragments for "click" chemical applications. Part 2. Formation of oligomers from orthogonally protected chiral trialkylsilylhomopropargyl azides and homopropargyl alcohols.
    Montagnat OD, Lessene G, Hughes AB.
    J Org Chem; 2010 Jan 15; 75(2):390-8. PubMed ID: 20000729
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  • 12. Remarkable access to fluoroalkylated trisubstituted alkenes via highly stereoselective cobalt-catalyzed hydrosilylation reaction of fluoroalkylated alkynes.
    Konno T, Taku K, Yamada S, Moriyasu K, Ishihara T.
    Org Biomol Chem; 2009 Mar 21; 7(6):1167-70. PubMed ID: 19262936
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  • 13. Catalytic asymmetric synthesis of chiral propargylic alcohols for the intramolecular Pauson-Khand cycloaddition.
    Turlington M, Yue Y, Yu XQ, Pu L.
    J Org Chem; 2010 Oct 15; 75(20):6941-52. PubMed ID: 20843029
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  • 15. Rhodium-catalyzed asymmetric one-pot transesterification and [2 + 2 + 2] cycloaddition leading to enantioenriched 3,3-disubstituted phthalides.
    Tanaka K, Osaka T, Noguchi K, Hirano M.
    Org Lett; 2007 Mar 29; 9(7):1307-10. PubMed ID: 17338538
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  • 17. Propargyl hydrazides: synthesis and conversion into pyrazoles through hydroamination.
    Yoshimatsu M, Ohta K, Takahashi N.
    Chemistry; 2012 Dec 03; 18(49):15602-6. PubMed ID: 23143924
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  • 18. Stereoselective formation of trisubstituted (Z)-chloroalkenes adjacent to a tertiary carbon stereogenic center by organocuprate-mediated reduction/alkylation.
    Narumi T, Kobayakawa T, Aikawa H, Seike S, Tamamura H.
    Org Lett; 2012 Sep 07; 14(17):4490-3. PubMed ID: 22900591
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  • 19. Propargyl alcohols as β-oxocarbenoid precursors for the ruthenium-catalyzed cyclopropanation of unactivated olefins by redox isomerization.
    Trost BM, Breder A, O'Keefe BM, Rao M, Franz AW.
    J Am Chem Soc; 2011 Apr 06; 133(13):4766-9. PubMed ID: 21401098
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  • 20. B(C6F5)3-catalyzed allylation of propargyl acetates with allylsilanes.
    Schwier T, Rubin M, Gevorgyan V.
    Org Lett; 2004 Jun 10; 6(12):1999-2001. PubMed ID: 15176803
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