Intramolekulare Diels-Alder-Reaktionen mit 2-Trimethylsiloxy-2-vinylcyclopropancarbonsäure-estern als Schlüsselbausteinen
- 1 December 1986
- journal article
- zuschrift
- Published by Wiley in Angewandte Chemie
- Vol. 98 (12) , 1104-1105
- https://doi.org/10.1002/ange.19860981213
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- 2-Alkenyl-substituted methyl 2-siloxycyclopropanecarboxylates as masked vinyl ketones: efficient syntheses of highly functionalized Michael adductsThe Journal of Organic Chemistry, 1985
- An approach to the synthesis of mevinolin based on intramolecular Diels-Alder cycloadditionThe Journal of Organic Chemistry, 1985
- Syntheses of (+)-.alpha.- and (+)-.beta.-eudesmol and their diastereomers by intramolecular nitrone-olefin cycloadditionThe Journal of Organic Chemistry, 1985
- A Synthesis of Norbisabolide via a Synthon Prepared by a Free Radical ReactionSynthetic Communications, 1984
- Ringöffnungsreaktionen von 2‐Siloxycyclopropancarbonsäuremethylestern zu 4‐OxoalkansäurederivatenEuropean Journal of Organic Chemistry, 1984
- Deprotonierung und diastereoselektive Alkylierung von 2‐siloxysubstituierten Cyclopropancarbonsäure‐methylesternEuropean Journal of Organic Chemistry, 1984
- The intramolecular Diels–Alder reaction: recent advances and synthetic applicationsCanadian Journal of Chemistry, 1984
- Intramolecular Diels-Alder and Alder Ene ReactionsPublished by Springer Nature ,1984