Donor–Acceptor Cyclopropanes as Three‐Carbon Components in a [4+3] Cycloaddition Reaction with 1,3‐Diphenylisobenzofuran
- 21 January 2008
- journal article
- research article
- Published by Wiley in Angewandte Chemie
- Vol. 47 (6), 1107-1110
- https://doi.org/10.1002/anie.200704438
Abstract
No abstract availableThis publication has 39 references indexed in Scilit:
- Synthesis of Trisubstituted 4-Oxepanones by the Lewis Acid-promoted Three-Component Ring-Expansion Reaction of Cyclopropapyranones, Silyl Enolates and GlyoxylatesHETEROCYCLES, 2001
- Lewis Acid-Promoted Cycloaddition Reaction of Cyclopropanes with Allylsilanes.CHEMICAL & PHARMACEUTICAL BULLETIN, 2001
- Lewis Acid-mediated Ring Expansion Reaction of 2,3-Methanochromanones with Silyl Enol EthersHETEROCYCLES, 1999
- [3+2] Cycloaddition of 2-Alkoxycyclopropyl Carbonyl Compounds with Enol Silyl Ethers for Functionalized Cyclopentane FormationSynlett, 1991
- Lewis Acid-Mediated Reaction of 2,2-Dialkoxycyclopropanecarboxylic Esters with Ketene Silyl Acetals. Synthesis of CyclopentenonesChemistry Letters, 1990
- Organische Reaktionen unter hohem Druck: Zum Mechanismus der homo‐Diels‐Alder‐Reaktion von Homofuran (2‐Oxabicyclo[3.1.0]hex‐3‐en)European Journal of Inorganic Chemistry, 1989
- Synthesis and Reactivity of Electrophilic CyclopropanesPublished by Wiley ,1987
- Cyclopropanone hemiacetalsChemical Reviews, 1983
- Alternative modes of addition of dienophiles to vinylcyclopropane systemsJournal of the Chemical Society, Chemical Communications, 1973
- Cycloadditionen desN-Methoxycarbonyl-2,3-homopyrrolsAngewandte Chemie, 1971