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Angewandte Chemie International Edition in English 1993, 32 Syntheses of Polycyclic Natural Products Employing the Intramolecular Double Michael Reaction. Synthese polycyclischer Naturstoffe durch intramolekulare doppelte Michael-Addition. Heterogeneous permanganate oxidations: Synthesis of medium ring keto-lactones via substituent directed oxidative cyclisation.

Jagattaran Das, Srinivasan Chandrasekaran.

Regioselective oxidative cleavage of functionalized unsymmetric tetraalkylstannanes via ozone. A regiocontrolled intramolecular O-cyclization. Decanolides, 10-membered lactones of natural origin.

Gerald Dräger, Andreas Kirschning, Ralf Thiericke, Marion Zerlin.

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Free radicals in the synthesis of medium-sized rings. New synthetic methodology for ring expansion of n-sized conjugated cycloalkenones into homoallylic n+3 lactones: 3-step synthesis of fragrant phoracantholide. Gary H Posner, Qiang Wang, Bethany A Halford, Jeffrey S Elias, John P Maxwell.Angewandte Chemie International Edition 2001, 40 Consecutive Three- and Four-Component Coupling Reactions with Anions Generated from a Butane Diacetal Desymmetrized Glycolic Acid Derivative.

A General Method for the Preparation of 9-, 10-, and 11-Membered Unsaturated Macrolides: Synthesis of 8-Propionyl-( Michael, Michael–aldol and Michael–Michael reactions of enolate equivalents of butane-2,3-diacetal protected glycolic acid derivatives. Medium-Sized Lactones: Short Synthesis of (−)-Phoracantholide-J. Sized 2-Cycloalkenones into Hydroxyolefinic New Silicon-Mediated, Sequential Ring Expansions of Angewandte Chemie International Edition 2006, 45 Umpolung Reactivity of Alkenyl Fischer Carbene Complexes, Copper Enolates, and Electrophiles.

José Barluenga, Abraham Mendoza, Alejandro Diéguez, Félix Rodríguez, Francisco J.

Oxidative fragmentation of bicyclic hydroxy silanes and stannanes: a strategy for the stereoselective synthesis of kainoids. Hebditch, Benjamin Read, Madeleine Helliwell. Russian Journal of Organic Chemistry 2014, 50 Medium- and large-ring lactones based on levoglucosenone. Formation of Contiguous Quaternary and Tertiary Stereocenters by Sequential Asymmetric Conjugate Addition of Grignard Reagents to 2-Substituted Enones and Mg-Enolate Trapping. There and back again: the synthetic travels of Gary H. Domino Ring Expansion: Regioselective Access to 9-Membered Lactones with a Fused Indole Unit from 2-Nitrophenyl-1,3-cyclohexanediones. David Reyes Loya, Alexandre Jean, Morgan Cormier, Catherine Fressigné, Stefano Nejrotti, Jérôme Blanchet, Jacques Maddaluno, Michaël De Paolis.The Ruthenium Tetraoxide-Promoted Oxidative Cleavage of β-Hydroxyethers. Efficient Entry into Medium-Ring Keto-Lactones. Phosphine-Mediated Annulation of Bis(enones): A Lewis Base Catalyzed “Mock Diels−Alder” Reaction. Andresen, Arun Ghosh, Kristina Dupont-Gaudet, and, Mélina Girardin. Ragan, Maxime Riou, Etienne Dauphin, Brian M. Michel Couturier, Fréderic Ménard, John A.Synthesis of gem-Difluoromethylenated Bicycloalkan-1-ols and Their Ring-Expansion to gem-Difluoromethylenated Macrocyclic Lactones. Teerachai Punirun, Krisana Peewasan, Chutima Kuhakarn, Darunee Soorukram, Patoomratana Tuchinda, Vichai Reutrakul, Palangpon Kongsaeree, Samran Prabpai, and Manat Pohmakotr.This article is cited by 43 publications.