Studies towards the total synthesis of solanoeclepin A: synthesis of the 7-oxabicyclo[2.2.1]heptane moiety and attempted seven-membered ring formation-Reference-Cited by-同舟云学术

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Studies towards the total synthesis of solanoeclepin A: synthesis of the 7-oxabicyclo[2.2.1]heptane moiety and attempted seven-membered ring formation

Published:2002-06-24 Issue:14 Volume: Page:1693-1700
ISSN:1472-7781
Container-title:Journal of the Chemical Society, Perkin Transactions 1
language:
Short-container-title:J. Chem. Soc., Perkin Trans. 1

Author:

Benningshof Jorg C. J.,Blaauw Richard H.,van Ginkel Angeline E.,van Maarseveen Jan H.,Rutjes Floris P. J. T.,Hiemstra Henk

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2002/P1/B201987F

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1. Parallel Kinetic Resolution of Intramolecular Furan Diels-Alder Cycloadducts via Asymmetric Hydroboration;European Journal of Organic Chemistry;2019-11-08

2. Rapid Access to the Structural Core of Aflavinines via Stereoselective Tandem Intramolecular Diels–Alder Cycloaddition Controlled by the Allylic 1,3-Strain;Organic Letters;2019-08-01

3. Asymmetric Synthesis of the DEFG Rings of Solanoeclepin A;Organic Letters;2019-01-14

4. Naturally Occurring Cyclobutanes: Their Biological Significance and Synthesis;Studies in Natural Products Chemistry;2018

5. Synthetic study toward the total synthesis of solanoeclepin A;Tetrahedron;2017-06

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