Photocycloadditionen mit α- und β-Naphthaldehyd: Vollständige Umkehr der Diastereoselektivität als Konsequenz unterschiedlich konfigurierter elektronischer Zustände
ChemInform Abstract: Photodecarboxylative Addition of Carboxylates and α-Keto Carboxylates to Phthalimides.
ChemInform Abstract: Stereoselective Yang Cyclizations of α-Amido Ketones.
ChemInform Abstract: Stereoselectivity of Triplet Photocycloadditions. Part 10. Oxazole—Carbonyl Photocycloadditions: Selectivity Pattern and Synthetic Route to erythro α-Amino,
ChemInform Abstract: Photodecarboxylative Additions of α-Keto Carboxylates to Phthalimides. Alkylation, Acylation, and Ring Expansion.
ChemInform Abstract: Azidohydroperoxidation of Pinenes: Stereoselectivity Pattern and the First X-Ray Structure of a 2-Azidohydroperoxide.
ChemInform Abstract: Reversible Diastereoselective Photocyclization of Phenylglyoxylamides of α-Amino Acid Methyl Esters to 3-Hydroxy β-Lactams.
ChemInform Abstract: Stereoselective Synthesis of 2-Aminocyclobutanols via Photocyclization of α-Amido Alkylaryl Ketones: Mechanistic Implications for the Norrish/Yang Reaction.
Singlet Oxygen Addition to Chiral Allylic Alcohols and Subsequent Peroxyacetalization with β-Naphthaldehyde: Synthesis of Diastereomerically Pure 3-β-Naphthyl-Substituted 1,2,4-Trioxanes.
Synthesis of Medium- and Large-Ring Compounds Initiated by Photochemical Decarboxylation of ω-Phthalimidoalkanoates
Synthesis of α-amino-3-chloro-4,5-dihydro-5-methyl-5-isoxazoleacetic acid, a ring-methylated analogue of the antitumor agent acivicin (AT-125)
Singlet oxygen addition to chiral allylic alcohols and subsequent peroxyacetalization with β-naphthaldehyde: synthesis of diastereomerically pure 3-β-naphthyl-substituted 1,2,4-trioxanes