Unexpected Hydroxyspirolactone Formation uponBaeyer-Villiger Oxidation of atrans-?-decalone (trans-octahydronaphthalen-1(2H)-one) and X-ray structure of the product-Reference-Cited by-同舟云学术

Unexpected Hydroxyspirolactone Formation uponBaeyer-Villiger Oxidation of atrans-?-decalone (trans-octahydronaphthalen-1(2H)-one) and X-ray structure of the product

Published:1995-06-28 Issue:4 Volume:78 Page:887-890
ISSN:0018-019X
Container-title:Helvetica Chimica Acta
language:de
Short-container-title:Helv. Chim. Acta

Author:

Demnitz F. W. Joachim,Freiberger Sabine,Weber Hans-Peter

Publisher

Wiley

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Drug Discovery,Biochemistry,Catalysis

Reference21 articles.

1. Convenient syntheses of 5,5,9-trimethyl-trans-1-decalone and 6.beta.-hydroxy-5,5,9.beta.-trimethyl-trans-1-decalone

2. J. Chem. Soc. 1957, 3441;

3. Syntheses in the Terpene Series. III.1 A Synthesis of 4,4,9-Trimethyl-trans-decal-8-one

4. A Synthesis of 2-Formyl-5,5,9-trimethyl-trans-Δ2-1-octalone

5. Zur Stereochemie der Geruchswahrnehmung von 1-Dekalon-Derivaten und ihren oxaanalogen Verbindungen

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1. Preparation of oxocene terpenes. The first enantiospecific synthesis of cytotoxic arenaran A;Organic & Biomolecular Chemistry;2016

2. ChemInform Abstract: Unexpected Hydroxyspirolactone Formation upon Baeyer-Villiger Oxidation of a trans-α-Decalone (trans-Octahydronaphthalen-1(2H)- one) and X-Ray Structure of the Product.;ChemInform;2010-08-17

3. Unexpected Rearrangement in the Peroxytrifluoroacetic Acid-Mediated Baeyer-Villiger Oxidation of trans-3.beta.-Hydroxy-4,4,10.beta.-trimethyl-9-decalone Forming a 7-Oxabicyclo[2.2.1]heptane. Structure Proof and Total Synthesis of (.+-.)-Farnesiferol-C;The Journal of Organic Chemistry;1995-08