69 research outputs found
An exploratory study on microwave-assisted solid-phase Diels-Alder reactions of 2(1H)-pyrazinones: the elaboration of a new tailor-made acid-labile linker
Generation of a small library of highly electron-rich 2-(Hetero)aryl-substituted phenethylamines by the Suzuki-Miyaura reaction: A short synthesis of an apogalanthamine analogue
Iridoids : enantioselective synthesis of loganin via an asymmetric diels-alder reaction
Starting from (-)-camphor-10-sulfonic acid (5) the crystalline sultam 9 was readily prepared. TiCl4-mediated Diels-Alder addition of the N-crotonoyl sultam 11 to cyclopentadiene, crys- tallization of the resulting adduct 12 and subsequent reduction gave virtually pure (1S, 4R, 5R, 6S)-1 together with recovered auxiliary 9. The loganin precursor 1 was transformed into norbornanone 20, which upon Baeyer-Villiger oxidation led to the suitably substituted cyclo- pentane 22 from which 1-B-O-methyl loganin aglucone (2) was rea- dily available
An efficient microwave-assisted solvent-free synthesis of pyrido-fused ring systems applying the tert-amino effect
Determination of the absolute configuration of three as-hydrindacene compounds by vibrational circular dichroism
Fully selective intramolecular ortho photocycloaddition of 4-(4-methoxyphenoxy)-3-(N3-benzoylthymin-1-yl)but-1-ene: An unprecedented benzene-thymine photocycloaddition
On irradiation of 4-(4-methoxyphenoxy)-3-(N-3-benzozylthymin-1-yl)but-1-ene 1 at 254 nm in THF a single photoadduct 2 is formed as a result of chemo-, regio- and stereo-selective intramolecular ortho photocycloaddition of the thymine double bond to the 1,2-positions of the phenyl ring.status: publishe
Sudan-β- d -glucuronides and their use for the histochemical localization of β-glucuronidase activity in transgenic plants
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