Florenci Vicent González Adelantado-rekin lankidetzan egindako argitalpenak (19)

2002

  1. Erratum: Stereoselective synthesis of the naturally occurring lactones (-)-osmundalactone and (-)-muricatacine using ring-closing metathesis (European Journal of Organic Chemistry (2002) (2649-2655))

    European Journal of Organic Chemistry

  2. Influence of the protecting groups on the syn/anti stereoselectivity of boron aldol additions with erythrulose derivatives. A theoretical and experimental study

    Tetrahedron, Vol. 58, Núm. 48, pp. 9697-9707

  3. Stereoselective synthesis of (-)-cytoxazone

    Tetrahedron Asymmetry, Vol. 13, Núm. 9, pp. 1005-1010

  4. Stereoselective synthesis of the naturally occurring lactones (-)-osmundalactone and (-)-muricatacine using ring-closing metathesis

    European Journal of Organic Chemistry, pp. 2649-2655

2001

  1. Chlorodicyclohexylborane-mediated aldol additions of α,α′-dioxygenated ketones

    Organic Letters, Vol. 3, Núm. 6, pp. 901-903

  2. Erratum: Stereoselective allylations of erythrulose derivatives under anhydrous conditions (Tetrahedron: Asymmetry (2001) 12 (1417-1429) PII: S0957416601002622)

    Tetrahedron Asymmetry

  3. Stereoselective allylations of erythrulose derivatives under anhydrous conditions

    Tetrahedron Asymmetry, Vol. 12, Núm. 10, pp. 1417-1429

2000

  1. A synthetic model for the [4+2] cycloaddition in the biosynthesis of the brevianamides, paraherquamides, and related compounds

    Tetrahedron, Vol. 56, Núm. 34, pp. 6345-6358

  2. Aldol reactions with erythrulose derivatives: Stereoselective synthesis of differentially protected syn-α,β-dihydroxy esters

    Tetrahedron, Vol. 56, Núm. 4, pp. 677-683

  3. Stereoselective synthesis of syn-α-methyl-β-hydroxy esters

    Tetrahedron Asymmetry, Vol. 11, Núm. 15, pp. 3211-3220

1999

  1. Boron aldol additions with erythrulose derivatives: Dependence of stereoselectivity on the type of protecting group

    Tetrahedron Letters, Vol. 40, Núm. 37, pp. 6845-6848

1998

  1. Diastereoselectivity in Organometallic Additions to the Carbonyl Group of Protected Erythrulose Derivatives

    Journal of Organic Chemistry, Vol. 63, Núm. 3, pp. 698-707

  2. Stereoselective synthesis of α-substituted serines from protected erythrulose oximes

    Tetrahedron Asymmetry, Vol. 9, Núm. 10, pp. 1703-1712

1997

  1. Diastereoselective additions of organolithium reagents to the C=N bond of protected erythrulose oxime ethers. Synthesis of enantiopure α,α-disubstituted α-aminoacids

    Tetrahedron Letters, Vol. 38, Núm. 10, pp. 1841-1844

  2. Diastereoselectivity of the reactions of organometallic reagents with protected D- and L-erythrulose 1,3-O-ethylidene acetals

    Tetrahedron Asymmetry, Vol. 8, Núm. 4, pp. 559-577

1996

  1. Synthesis of protected enantiopure erythrulose derivatives

    Liebigs Annales, pp. 1801-1810

1995

  1. Synthesis of (E)-2,6-dimethyl-6-hydroxyocta-2,7-dienoic acid and the corresponding amide ("acacialactam") in optically active form

    Tetrahedron, Vol. 51, Núm. 9, pp. 2755-2762

1993

  1. Highly diastereoselective additions of organometallic reagents to 1-O-silylated 3,4-Di-O-benzyl-L-erythrulose derivatives

    Tetrahedron: Asymmetry, Vol. 4, Núm. 8, pp. 1799-1802

1992

  1. Diastereoselective synthesis of enantiomeric tertiary alcohols via nucleophilic additions to protected D- and L-erythrulose derivatives

    Tetrahedron: Asymmetry, Vol. 3, Núm. 12, pp. 1511-1514