An organometallic route to (±)3-p-toluenesulfinyl- 2-pyrone
Author:
Publisher
Elsevier BV
Subject
Materials Chemistry,Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Reference21 articles.
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2. Enantiocontrolled synthesis of quaternary carbon centers. 3,3-Disubstituted cyclopentanones. (+)-α-cuparenone.
3. Enantiocontrolled synthesis of ()-3-substituted cycloalkanones from ()-2-(-tolylsulfinyl)-2-cycloalkenones and diorganomagnesium reagents.
4. Asymmetric synthesis using enantiomerically pure 2-(p-anisylsulfinyl)-2-cycloalkenones
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1. A natural light induced regioselective 6π-electrocyclisation–oxidative aromatisation reaction: experimental and theoretical insights;Organic & Biomolecular Chemistry;2008
2. Halogenated-2-pyrones in Sonogashira cross-coupling: limitations, optimisation and consequences for GC analysis of Pd-mediated reactions;Tetrahedron;2005-10
3. Development of Base Catalyzed Diels-Alder Reaction of 3-Hydroxy-2-pyrone and Application to Synthesis of Biologically Active Compounds.;Journal of Synthetic Organic Chemistry, Japan;1999
4. Chiral sulfinyl-1,3-dienes. Synthesis and use in asymmetric reactions;Tetrahedron: Asymmetry;1997-05
5. Diels-Alder cycloadditions of 2-pyrones and 2-pyridones;Tetrahedron;1992-01
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