José Manuel Odriozola Ibarguren-rekin lankidetzan egindako argitalpenak (32)

2023

  1. Development of an α′-hydroxy enone for the aminocatalytic asymmetric formal conjugate addition of aldehydes to acrylates, vinyl ketones and acrolein

    Organic and Biomolecular Chemistry, Vol. 21, Núm. 23, pp. 4833-4845

  2. Organocatalytic Michael Addition of Unactivated α-Branched Nitroalkanes to Afford Optically Active Tertiary Nitrocompounds

    Organic Letters, Vol. 25, Núm. 48, pp. 8590-8595

2019

  1. Enantioselective Addition of Alkynyl Ketones to Nitroolefins Assisted by Brønsted Base/H-Bonding Catalysis

    Chemistry - A European Journal, Vol. 25, Núm. 17, pp. 4390-4397

2018

  1. α-Hydroxy Ketones as Masked Ester Donors in Brønsted Base Catalyzed Conjugate Additions to Nitroalkenes

    Chemistry - A European Journal, Vol. 24, Núm. 15, pp. 3893-3901

2016

  1. Asymmetric Assembly of All-Carbon Tertiary/Quaternary Nonadjacent Stereocenters through Organocatalytic Conjugate Addition of α-Cyanoacetates to a Methacrylate Equivalent

    Chemistry - A European Journal, Vol. 22, Núm. 38, pp. 13690-13696

2014

  1. Catalytic Enantioselective Quick Route to Aldol-Tethered 1,6- and 1,7-Enynes from ω-Unsaturated Aldehydes

    Chemistry - A European Journal, Vol. 20, Núm. 47, pp. 15543-15554

  2. Enantioselective construction of tetrasubstituted stereogenic carbons through brønsted base catalyzed michael reactions: α′-hydroxy enones as key enoate equivalent

    Journal of the American Chemical Society, Vol. 136, Núm. 51, pp. 17869-17881

2013

  1. Asymmetric synthesis of propargylic alcohols via aldol reaction of aldehydes with ynals promoted by prolinol ether-transition metal-Brønsted acid cooperative catalysis

    Chemical Science, Vol. 4, Núm. 8, pp. 3198-3204

2010

  1. (1R)-(+)-camphor and acetone derived α′-hydroxy enones in asymmetric diels-alder reaction: Catalytic activation by Lewis and brønsted acids, substrate scope, applications in syntheses, and mechanistic studies

    Journal of Organic Chemistry, Vol. 75, Núm. 5, pp. 1458-1473

2009

  1. Conjugate Addition of Nitroalkanes to an Acrylate Equivalent. Stereocontrol at C-α of the Nitro Group through Double Catalytic Activation

    Organic Letters, Vol. 11, Núm. 17, pp. 3826-3829

2008

  1. Catalytic Michael reactions of ketoesters with a camphor-derived acrylate equivalent: Stereoselective access to all-carbon quaternary centers

    Organic Letters, Vol. 10, Núm. 13, pp. 2637-2640

  2. Copper-catalyzed enantioselective conjugate addition of dialkylzinc reagents to α′-oxy enones

    Chemistry - A European Journal, Vol. 14, Núm. 29, pp. 8768-8771

2005

  1. Asymmetric propionate aldol reactions of a chiral lithium enolate accessible from direct enolization with n-butyllithium

    Arkivoc, Vol. 2005, Núm. 6, pp. 377-392

2004

  1. A practical total synthesis of hapalosin, a 12-membered cyclic depsipeptide with multidrug resistance-reversing activity, by employing improved segment coupling and macrolactonization

    Journal of Organic Chemistry

2002

  1. Design and synthesis of a novel class of sugar-peptide hybrids: C-linked glyco β-amino acids through a stereoselective "acetate" Mannich reaction as the key strategic element

    Journal of the American Chemical Society, Vol. 124, Núm. 29, pp. 8637-8643

1995

  1. Diastereoselective [2+2] cycloaddition of dichloroketene with α-oxyaldehydes and α-amino aldehydes

    Journal of the Chemical Society, Chemical Communications, pp. 1735-1736

1994

  1. Concise General Synthesis of α,γ-Disubstituted β-Amino Ketones from β-Lactams

    Journal of Organic Chemistry, Vol. 59, Núm. 18, pp. 5184-5188

  2. From (S)-α-amino β-hydroxyacids to (R)-α,β-diamino-γ-hydroxyacid N-carboxyanhydrides via β-lactams

    Tetrahedron Letters, Vol. 35, Núm. 17, pp. 2725-2728

  3. Synthesis of β-alkylserine-N-carboxyanhydrides through β-lactams via cycloaddition reaction of alkoxyketenes to chiral α-alkoxyaldehyde-derived imines

    Tetrahedron Letters, Vol. 35, Núm. 17, pp. 2721-2724

1993

  1. Asymmetric synthesis of α-keto β-lactams via [2+2] cycloaddition reaction: A concise approach to optically active (α-hydroxy β-lactams and β-alkyl(aryl)isoserines.

    Tetrahedron Letters, Vol. 34, Núm. 39, pp. 6325-6328