Artículos (12) Publicaciones en las que ha participado algún/a investigador/a

1992

  1. 2-(Chloromethyl)-3-tosylpropene: An useful reagent for the synthesis of allyl sulfones

    Tetrahedron, Vol. 48, Núm. 24, pp. 5179-5190

  2. Anodic oxidation of isopropyl and tert-butylbenzenes. Synthetic routes to certain cyclohexa-1,4-dienes

    Tetrahedron, Vol. 48, Núm. 45, pp. 9967-9976

  3. Arene 1,4-diradical formation from o-dialkynylarenes

    Tetrahedron Letters, Vol. 33, Núm. 23, pp. 3277-3280

  4. Arene-catalysed reductive lithiation of tetrahydrofuran: improved synthesis of 1,5-diols

    Tetrahedron, Vol. 48, Núm. 17, pp. 3585-3588

  5. Cycloadditions of 2-nitro 1,3-dienes to enamines. Asymmetric induction and synthesis of unsaturated nitroketones and diels-alder adducts via [4+2] heterocyloadditions.

    Tetrahedron Letters, Vol. 33, Núm. 38, pp. 5641-5644

  6. Dilithiation of 2-(chloromethyl)-3-tosylpropene: Synthesis and reactivity of a new chlorinated allyl sulfone dianion

    Tetrahedron Letters, Vol. 33, Núm. 43, pp. 6543-6546

  7. Easy synthesis of 2,4-dialkyl substituted phenols and anisoles from p-bensoquinone

    Tetrahedron, Vol. 48, Núm. 13, pp. 2709-2714

  8. Homoenolic radical derived from propionic acid: A versatile reagent for the radical version of the Michael reaction

    Tetrahedron, Vol. 48, Núm. 43, pp. 9531-9536

  9. Naphthalene-catalysed lithiation of 3-chloro-2-chloromethyl-propene: A barbier-type practical alternative to the trimethylenemethane dianion

    Tetrahedron Letters, Vol. 33, Núm. 16, pp. 2217-2220

  10. Naphthalene-catalysed lithiation of allylic and benzylic mesylates: a new method for allyl, methallyl, and benzyl lithium

    Tetrahedron, Vol. 48, Núm. 22, pp. 4593-4600

  11. Naphthalene-catalysed lithiation of dialkyl sulfates: A new route for organolithium reagents

    Tetrahedron Letters, Vol. 33, Núm. 38, pp. 5597-5600

  12. One-Step Synthesis of Substituted 6,8-Dioxabicyclo[3.2.1]octanes: Easy Preparation of Racemic Frontalin, Brevicomins, and Related Systems

    Journal of Organic Chemistry, Vol. 57, Núm. 2, pp. 750-751