Asymmetric Synthesis of Highly Functionalized 8-Oxabicyclo[3.2.1]octene Derivatives
- 1 January 1996
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 118 (44), 10774-10782
- https://doi.org/10.1021/ja962081y
Abstract
No abstract availableKeywords
This publication has 45 references indexed in Scilit:
- [3 + 4] and [3 + 5] Annulation Reactions of .alpha.-(Phenylthio)Dicarbonyl Electrophiles with Bis(trimethylsilyl) Enol Ethers: Synthesis of Highly Functionalized Medium Ring CarbocyclesThe Journal of Organic Chemistry, 1995
- Total Synthesis of Furanether B. An Application of a [3 + 4] Annulation StrategyThe Journal of Organic Chemistry, 1995
- Convenient Synthesis of Vinyldiazomethanes from α-Diazo-β-Keto Esters and Related SystemsSynthetic Communications, 1992
- A novel concept for regiochemical and stereochemical control in Lewis acid promoted [3 + 4] annulation reactionsThe Journal of Organic Chemistry, 1991
- Pseudoguaianolides from intramolecular cycloadditions of aryl diazoketones: synthesis of (±)-confertin and an approach to the synthesis of (±)-damsinJournal of the Chemical Society, Perkin Transactions 1, 1991
- Opening of oxabicyclo[3.2.1]octenes with organolithium reagents. A route to cyclic and acyclic compounds with high stereocontrolThe Journal of Organic Chemistry, 1990
- Scope and stereochemistry of the tandem intramolecular cyclopropanation/Cope rearrangement sequenceThe Journal of Organic Chemistry, 1989
- Diazotransfer Reactions withp-Acetamidobenzenesulfonyl AzideSynthetic Communications, 1987
- An Example of the influence of Stereochemistry of a Proximate Methyl Substituent on Keto-Enol TautomerismTetrahedron, 1984
- Total synthesis of (±)-β-bulnesene, (±)-cryptofauronol, (±)-fauronyl acetate, and (±)-valeranoneJournal of the Chemical Society, Chemical Communications, 1983