The Phenanthrenone Approach to Opium Alkaloids: Formal Total Synthesis of Morphine by Sigmatropic Rearrangement. -Eschenmoser-Claisen rearrangement of alcohol (II) and ring closure reaction of epoxide (VII) to give the desired E-ring are the key steps in the preparation of the morphine synthon (VII
✦ LIBER ✦
ChemInform Abstract: Formal Synthesis of ent-Dysiherbaine from Sulfinyl Dihydropyrans by Sigmatropic Rearrangement and Tethered Aminohydroxylation.
✍ Scribed by Roberto Fernandez de la Pradilla; Nadia Lwoff; Alma Viso
- Publisher
- John Wiley and Sons
- Year
- 2008
- Weight
- 20 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0931-7597
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✦ Synopsis
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 via the “References” option.
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ChemInform Abstract: The Phenanthrenone
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J. MULZER; J. W. BATS; B. LIST; T. OPATZ; D. TRAUNER
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Article
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2010
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John Wiley and Sons
⚖ 31 KB
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