Asymmetric Photocycloadditions with Optically Pure, Spirocyclic Enones. Simple Synthesis of (+)‐ and (−)‐Grandisol
- 1 December 1986
- journal article
- research article
- Published by Wiley in Angewandte Chemie International Edition in English
- Vol. 25 (12) , 1117-1119
- https://doi.org/10.1002/anie.198611171
Abstract
No abstract availableKeywords
This publication has 16 references indexed in Scilit:
- 1,3‐Dioxanone Derivatives from β‐Hydroxy‐carboxylic Acids and Pivalaldehyde. Versatile Building Blocks for Syntheses of Enantiomerically Pure Compounds. A Chiral Acetoacetic Acid Derivative Preliminary CommunicationHelvetica Chimica Acta, 1986
- Synthesis of natural products based on photochemical key transformationsPublished by Walter de Gruyter GmbH ,1986
- Efficient asymmetric (2 + 2) photocycloaddition leading to chiral cyclobutanes. Application to the total synthesis of (-)-grandisolJournal of the American Chemical Society, 1986
- Asymmetric induction in simple [2 + 2] photoadditionsTetrahedron Letters, 1985
- Tereoselective total synthesis of racemic grandisolTetrahedron, 1985
- Enone Photochemical Cycloaddition in Organic SynthesisPublished by Springer Nature ,1984
- Meldrum's acid in organic synthesis. 2. A general and versatile synthesis of .beta.-keto estersThe Journal of Organic Chemistry, 1978
- Synthesis of the both enantiomers of grandisol, the boll weevil pheromoneTetrahedron, 1978
- Versuche mit „Meldrums Säure”︁ und anderen cyclischen Estern (Acylalen) von MalonsäurenEuropean Journal of Inorganic Chemistry, 1961
- Carbon Syntheses with Malonic Acid and Related Compounds. II. Aromatic AldehydesJournal of the American Chemical Society, 1936