ALFONSO GONZALEZ ORTEGA-rekin lankidetzan egindako argitalpenak (25)

2016

  1. ChemInform Abstract: Synthesis of Azepane Derivatives by Silyl-Aza-Prins Cyclization of Allylsilyl Amines: Influence of the Catalyst in the Outcome of the Reaction.

    ChemInform, Vol. 47, Núm. 38

  2. Synthesis of Azepane Derivatives by Silyl-aza-Prins Cyclization of Allylsilyl Amines: Influence of the Catalyst in the Outcome of the Reaction

    Organic Letters, Vol. 18, Núm. 9, pp. 1972-1975

2015

  1. ChemInform Abstract: Efficient Access to Polysubstituted Tetrahydrofurans by Electrophilic Cyclization of Vinylsilyl Alcohols.

    ChemInform, Vol. 46, Núm. 41, pp. no-no

  2. Efficient access to polysubstituted tetrahydrofurans by electrophilic cyclization of vinylsilyl alcohols

    RSC Advances, Vol. 5, Núm. 61, pp. 49541-49551

2014

  1. Competitive Silyl-Prins Cyclization versus Tandem Sakurai-Prins Cyclization: An Interesting Substitution Effect

    Chemistry - A European Journal, Vol. 20, Núm. 43, pp. 14112-14119

2012

  1. Efficiency of acid- and mercury-catalyzed cyclization reactions in the synthesis of tetrahydrofurans from allylsilyl alcohols

    European Journal of Organic Chemistry, pp. 5350-5356

2010

  1. A new synthetic approach to 3-methylene-1-cyclohexanols fused to five-, six- and seven-membered carbocycles through intramolecular cyclization of epoxyallylsilanes

    Arkivoc, Vol. 2010, Núm. 3, pp. 274-287

2001

  1. Synthesis of [1]Benzopyrano[4,3-b]pyrrol-4(1H)-ones from 4-chloro-3-formylcoumarin

    Synthesis, pp. 1941-1948

1994

  1. Synthesis of [1]benzopyrano[4,3-b]pyrrol-4(1H)-ones from 4-chlorocoumarin

    Synthesis, pp. 279-281

1992

  1. A new chiral glycine synthon. Synthesis, x-ray structure of (-).(2S,4R)-2-ethoxycarbonyl-4-phenyl-1,3-oxazolidine and diastereoselective nucleophilic ring opening to (R)-ethyl α-amino carboxylates.

    Tetrahedron Letters, Vol. 33, Núm. 33, pp. 4743-4746

  2. Stereoselective ring opening of chiral oxazolidines by reformatsky reagents: an enantioselective entry to β-amino esters.

    Tetrahedron Letters, Vol. 33, Núm. 20, pp. 2895-2898

1991

  1. An improved synthesis of 2H-1,2,6-thiadiazine 1,1-dioxides by condensation of β-amino and β-chloro α,β-unsaturated ketones with sulfamides

    Synthesis, pp. 355-356

1990

  1. Alkylation of 3,5-dimethylisothiazole.a regioselective synthesis of 5-alkyl-3-methylisothiazoles.

    Synthetic Communications, Vol. 20, Núm. 4, pp. 617-624

  2. An efficient synthesis of 3-tert-aminopropanol derivatives by regioselective ring opening of tetrahydro-1,3-oxazines with grignard reagents.

    Synthetic Communications, Vol. 20, Núm. 8, pp. 1149-1158

  3. Differential reactivity of β-amino enones and 3-dimethylaminoacrylaldehyde towards α-amino derivatives

    Journal of the Chemical Society, Perkin Transactions 1, pp. 2681-2685

  4. Some observations on the regioselective ring opening of tetrahydro-1,3-oxazinium methiodides by sodium borohydride in alcoholic and ethereal solvents

    Heterocycles, Vol. 31, Núm. 11, pp. 2079-2084

  5. The reaction of β-aminoenones with α-amino derivatives. Synthesis of 2-functionalized pyrroles

    Heterocycles, Vol. 31, Núm. 6, pp. 1049-1058

1989

  1. Regioselective synthesis of 2- and 3-acylpyrroles by reaction of β-aminoenones with α-aminoketone hydrochloride

    Heterocycles, Vol. 29, Núm. 10, pp. 1983-1991

  2. Some observations on the reactivity of β-aminoenones towards phenacylamine hydrochloride

    Heterocycles, Vol. 29, Núm. 10, pp. 1973-1982

1988

  1. Reaction of 2H-1-benzopyrans with organometallic reagents. Synthesis of 4-(α, γ-dialkyl-β-4-methoxyphenylallyl) resorcins

    Heterocycles, Vol. 27, Núm. 2, pp. 393-399