First Total Synthesis of (±)-6′-Methoxyretrojusticidin B Using Regiocontrolled Benzannulation: Structural Inconsistency with Procumphthalide A and Its Revision to 5′-Methoxyretrochinensin
Author:
Publisher
Georg Thieme Verlag KG
Subject
Organic Chemistry
Link
http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0030-1258529.pdf
Cited by 6 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. Asymmetric Total Synthesis of a Bioactive Lignanamide Using a 5‐ endo ‐ tet ‐Type Cyclization of Activated Cyclopropylcarbinols and Synthetic Support for the Reaction Mechanism;European Journal of Organic Chemistry;2022-07-28
2. From Enantioenriched Donor‐Acceptor Cyclopropylcarbinols to Axially Chiral Arylnaphthalenes through Aryldihydronaphthalenes: Central‐to‐Axial Chirality Exchange;European Journal of Organic Chemistry;2021-11-23
3. Stereochemical Courses and Mechanisms of Ring-opening Cyclization of Donor–Acceptor Cyclopropylcarbinols and Cyclization of 7-Benzyloxy Dibenzyl Lignan Lactones;Chemistry Letters;2017-04-05
4. Cyclohexanes;Cyclopropanes in Organic Synthesis;2015-10-02
5. Highly Stereoselective Carbon–Carbon Bond-forming Reactions on Cyclopropane Rings Using 1-(Methoxycarbonyl)cyclopropylzinc Bromides;Chemistry Letters;2015-06-05
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