Spiroketals via Oxidative Rearrangement of Enol Ethers.
✍ Scribed by David L. Waller; Cory R. J. Stephenson; Peter Wipf
- Publisher
- John Wiley and Sons
- Year
- 2007
- Weight
- 35 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0931-7597
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✦ Synopsis
Abstract
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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
## Abstract Reaction of the monomethyl enol ethers of 3‐chloro‐2,4‐pentanedione and 2‐chloro‐1‐phenyl‐1,3‐butanedione with sodium methoxide in methanol gave hydroxy enol ethers, respectively 3‐hydroxy‐2,4,4‐trimethoxy‐1‐pentene and 3‐hydroxy‐2,4,4‐trimethoxy‐4‐phenyl‐1‐butene. The reaction mechanis