Über innermolekulare Umlagerungen in der Bicyclo‐[1.2.2]‐heptan‐Reihe, VIII. Die Hydratisierung der beiden stereoisomeren trans ‐3‐Methyl‐bicyclo‐[1.2.2]‐hepten‐(5)‐carbonsäuren‐(2)
Author:
Affiliation:
1. Chemisches Institut der Landwirtschaftlichen Hochschule Stuttgart‐Hohenheim
Publisher
Wiley
Subject
Inorganic Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/cber.19590921006
Reference14 articles.
1. Über innermolekulare Umlagerungen in der Bicyclo‐[1.2.2]‐heptan‐Reihe, VII. Synthese und Hydratisierung zweier stereoisomerer 2.3‐Dimethyl‐bicyclo‐[1.2.2]‐hepten‐(5)‐carbonsäuren‐(2)
2. Über Zwei Stereoisomere 3‐Methyl‐Norborneole
3. Über die diastereomeren 2‐Methyl‐norborneole
4. Über innermolekulare Umlagerungen in der Bicyclo-[1,2,2]-heptan-Reihe. IV. Die Hydratisierung des Norcamphens und 2-Methyl-bicyclo-[1,2,2]-heptens-(2) und die diastereomeren 1-Methyl-norborneole
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1. Methods for the construction of trans-hydrindane rings and their origins in steroid chemistry. Vitamin D total synthesis;Tetrahedron;1998-10
2. Stereoselective synthesis of cyclopentanones by reductive cleavage of 6-oxonorbornane-2-carboxylates and its application to the synthesis of 1.alpha.,25-dihydroxyvitamin D3 CD ring;The Journal of Organic Chemistry;1993-03
3. Synthesis of vitamin D3 D ring synthons by reductive cleavage of norbornan-6-one-2-carboxylates;Tetrahedron Letters;1990-01
4. Synthesis of 2,2-disubstituted 7-methylenenorbornanes with 2-exo functionality by Diels-Alder reaction of 5,5-dimethoxytetrachlorocyclopentadiene;The Journal of Organic Chemistry;1985-06
5. Camphor: a chiral starting material in natural product synthesis;Natural Product Reports;1985
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