Acid-catalyzed rearrangement of laureatin to isolaureatin and related reactions. XVIII
Author:
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo00969a037
Cited by 11 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. A Unifying Stereochemical Analysis for the Formation of Halogenated C15-Acetogenin Medium-Ring Ethers From Laurencia Species via Intramolecular Bromonium Ion Assisted Epoxide Ring-Opening and Experimental Corroboration with a Model Epoxide;The Journal of Organic Chemistry;2012-10-22
2. Asymmetric Total Syntheses of (+)-3-(Z)-Laureatin and (+)-3-(Z)-Isolaureatin by “Lone Pair−Lone Pair Interaction-Controlled” Isomerization;Journal of the American Chemical Society;2007-02-01
3. Biosynthesis of Cyclic Bromoethers from Red Algae;Comprehensive Natural Products Chemistry;1999
4. Isomerization of the (Z)-Enyne Unit to the (E)-Enyne Unit. Conversion of Laureatin to (E)-Isolaureatin;Chemistry Letters;1994-08
5. Radiation-initiated addition of acetaldehyde to allylalcohol and conversion of the 1:2-telomer into 1-methyl-2,8-dioxabicyclo[4,2,1]nonane;Collection of Czechoslovak Chemical Communications;1989
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