Search Results - "Grima, Pedro M"
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Use of the p-Tolylsulfinyl Group as a Chiral Inductor in Stereoselective [4+3] Cycloaddition Reactions: Preparation of Enantiopure Polysubstituted 8-Oxabicyclo[3.2.1]oct-6-en-3-one Systems Having up to Five Stereocenters
Published in European journal of organic chemistry (01-05-2014)“…The use of the p‐tolylsulfinyl group as a chiral inductor in stereoselective [4+3] cycloaddition reactions has made possible the preparation of enantiopure…”
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[4+3] Cycloaddition of C-3 substituted furans. Stereoselectivity induced by coordination effects
Published in Tetrahedron (02-12-2012)“…Several C-3 substituted furans with chelating groups have been reacted with 2,3-dibromo-3-pentanone in the presence of a reducing metal, resulting in the…”
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Discovery of a novel class of zwitterionic, potent, selective and orally active S1P1 direct agonists
Published in Bioorganic & medicinal chemistry letters (15-12-2012)“…Amido-1,3,4-thiadiazoles were identified as a novel structural class of potent and selective sphingosine-1-phosphate receptor subtype-1 agonists. Starting from…”
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Study of cis/trans and endo/exo Diastereoselectivity in the [4+3]-Cycloaddition Reaction of 2-Functionalized Furans and Dimethyloxyallyl Cation: Preparation of Versatile Cycloheptane Synthons
Published in Chemistry letters (01-09-1997)“…A study on the influence of steric and electronic effects of a function attached at C-2 of furans in the yield and diastereoselectivity of [4+3] cycloaddition…”
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Asymmetry induction on the [4C(4π)+3C(2π)] cycloaddition reaction of C2-functionalized furans: influence of the chiral auxiliary nature
Published in Tetrahedron (10-06-2002)“…The study of the π-facial diastereoselectivity in the [4+3] cycloaddition reaction of thirteen different chiral 2-substituted furans with oxyallyl cations,…”
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Induction of asymmetry on the [4+3] cycloaddition reaction of C2-functionalized furans
Published in Tetrahedron letters (11-03-2002)“…A study of the induction of asymmetry on the [4+3] cycloaddition reaction of some 13 C2-substituted furan derivatives with 2-oxyallyl cation is presented. The…”
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Effective, Safe, and Inexpensive Microscale Ultrasonic Setup for Teaching and Research Laboratories
Published in Journal of chemical education (01-06-2000)“…Presents a homemade, safe, effective, and inexpensive reactor vessel for ultrasonic horns with applications in microscale experiments in teaching and research…”
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Effective, Safe, and Inexpensive Microscale Ultrasonic Setup for Teaching and Research Labs
Published in Journal of chemical education (01-06-2000)“…Ultrasound has been used as a source of energy in chemical reactions to increase both reaction rate and product yield. Ultrasonic horns can be used for this…”
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New methodology for the synthesis of tetrahydrofuro[3,2-b]furan-2(3H)-one derivatives, synthons of natural products with biological interest
Published in Tetrahedron (27-10-2016)“…A new methodology is presented to synthesize in a regio and stereoselective manner tetrahydrofuro[3,2-b]furan-2(3H)-one, structural subunit present in a wide…”
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Synthesis of C3-substituted enantiopure 2-(p-tolylsulfinyl)-furans: the sulfoxide group as a chiral inductor for furan dienes as precursors of a wide variety of chiral intermediates
Published in Tetrahedron: asymmetry (30-04-2014)“…(−)-(1R,2S,5R)-Menthyl (SS)-p-toluenesulfinate and its enantiomer are a common source for a chiral sulfoxide group in organic synthesis, by means of…”
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Generation of Oxyallyl Cations by Reduction of α,α′-Diiodoketones Under Sonochemical or Thermal Conditions: Improved Methodology for the [4C(4π;)+3C(2π;)] Cycloaddition Reactions
Published in Synthetic communications (01-03-2003)“…An improved methodology to carry out [4C(4π;)+3C(2π;)] cycloaddition reactions of dienes and oxyallyl cations, is presented. The reaction starts from…”
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New synthetic methodology to prepare polyfunctionalized heptane building blocks with four stereocenters: synthesis of the (±)-C17–C23 subunit of Ionomycin
Published in Tetrahedron letters (12-02-1999)“…A new synthetic methodology for preparing polyfunctionalized heptane building blocks with up to four stereocenters has been developed…”
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2-Functionalized furans as precursors of versatile cycloheptane synthons
Published in Tetrahedron (25-08-1997)“…An study on the influence of steric and electronic effects of a function attached at C-2 of furans in the yield and diastereoselectivity of [4 + 3]…”
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Complete assignment of 1H and 13C NMR data and establishment of the relative stereochemistry of C-1-functionalized 2,4-dimethyl-8-oxabicyclo[3.2.1] oct-6-en-3-one derivatives
Published in Magnetic resonance in chemistry (01-07-1999)“…The total assignment of the 1H and 13C NMR spectra of 24 cis‐endo and 15 cis‐exo diastereoisomers of C‐1‐substituted…”
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Study of cis/trans and endo/exo Diastereoselectivity in the [4+3]-Cycloaddition Reaction of 2-Functionalized Furans and Dimethyloxyallyl Cation
Published in Chemistry letters (01-09-1997)“…A study on the influence of steric and electronic effects of a function attached at C-2 of furans in the yield and diastereoselectivity of [4+3] cycloaddition…”
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General method of assignment of relative stereochemistry in C-1-substituted 2,4-dimethyl-8-oxabicyclo[3.2.1]oct-6-en-3-one by 1H and 13C NMR correlations
Published in Magnetic resonance in chemistry (01-03-1998)“…The 1H and 13C NMR spectra of cis‐endo (a) and cis‐exo (b) diastereoisomeric pairs of five differently C‐1‐functionalized…”
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