An Enantioselective Total Synthetic Approach to (+)-Heptemerone G and (+)-Guanacastepene A from 2-Furyl Methyl Carbinol-Reference-Cited by-同舟云学术

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An Enantioselective Total Synthetic Approach to (+)-Heptemerone G and (+)-Guanacastepene A from 2-Furyl Methyl Carbinol

Published:2013-06-06 Issue:11 Volume:24 Page:1387-1390
ISSN:0936-5214
Container-title:Synlett
language:en
Short-container-title:Synlett

Author:

Wicha Jerzy,Michalak Karol

Publisher

Georg Thieme Verlag KG

Subject

Organic Chemistry

Link

http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0033-1338857.pdf

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2. Efficient Piancatelli rearrangement on a large scale using the Zippertex technology under subcritical water conditions;Reaction Chemistry & Engineering;2022

3. Recent Advances on Piancatelli Reactions and Related Cascade Processes;Synthesis;2021-11-15

4. C ₁-Symmetric Ligand-Enabled Stereoselective Formal [5+4] Cycloadditions of Palladium-Containing 1,5-Carbodipoles;SSRN Electronic Journal;2020

5. Development of a catalytic enantioselective synthesis of the guanacastepene and heptemerone tricyclic core;Tetrahedron;2019-06

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