Aldol-type transformations of levoglucosenone-derived medium-sized keto lactones
Author:
Publisher
Elsevier BV
Subject
General Chemistry
Reference38 articles.
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5. Stereoelectronic and steric control in chiral cyclohexane synthesis toward (−)-tetrodotoxin
Cited by 3 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. Michael Adducts of Levoglucosenone with α-Ethoxycarbonyl- and α-Nitrocyclododecanones: Transformation into Chiral Macrolides;Chemistry of Heterocyclic Compounds;2020-11
2. Reverse ketal-acetal rearrangement of levoglucosenone and cyclohexanone Michael adducts and the possibilities of its use in the synthesis of native topology lactones;Chemistry of Heterocyclic Compounds;2019-07
3. Reversible intramolecular Dieckmann-type condensation of 2-(2-hydroxymethyl-5,5,6-trimethoxytetrahydropyran-3-ylcarbonyl)-cyclopentanone: an alternative access to medium-sized lactones;Mendeleev Communications;2019-01
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