Highly chemo- and regioselective rearrangement of α,β-epoxy ketones to 1,3-dicarbonyl compounds in 5 mol dm−3 lithium perchlorate–diethyl ether medium-Reference-Cited by-同舟云学术

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Highly chemo- and regioselective rearrangement of α,β-epoxy ketones to 1,3-dicarbonyl compounds in 5 mol dm−3 lithium perchlorate–diethyl ether medium

Published:1999 Issue:21 Volume: Page:3173-3175
ISSN:0300-922X
Container-title:Journal of the Chemical Society, Perkin Transactions 1
language:
Short-container-title:J. Chem. Soc., Perkin Trans. 1

Author:

Sankararaman S.,Nesakumar J. E.

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/1999/P1/A905619J

Cited by 19 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. Access to Naphthoic Acid Derivatives through an Oxabenzonorbornadiene Rearrangement;Organic Letters;2023-10-05

2. Selective Oxidative Cleavage of the C–C Bond in α,β-Epoxy Ketone into Carbonyl Compounds;ACS Omega;2022-06-10

3. Triflic‐Acid‐Catalyzed Tandem Epoxide Rearrangement and Annulation with Alkynes: An Efficient Approach for Regioselective Synthesis of Naphthalenes;ChemistrySelect;2022-03-04

4. Rhenium complex-catalyzed Meinwald rearrangement reactions of oxiranes;Tetrahedron Letters;2017-06

5. Room-Temperature Coupling/Decarboxylation Reaction of α-Oxocarboxylates with α-Bromoketones: Solvent-Controlled Regioselectivity for 1,2- and 1,3-Diketones;The Journal of Organic Chemistry;2017-01-18

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