Synthesis of functionalized cyclotriveratrylene analogues with C1-symmetry and the application for 1,4-Michael addition of alcohols to unsaturated aryl ketone-Reference-Cited by-同舟云学术

Synthesis of functionalized cyclotriveratrylene analogues with C1-symmetry and the application for 1,4-Michael addition of alcohols to unsaturated aryl ketone

Published:2013-09 Issue:35 Volume:69 Page:7308-7313
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Song Jing-Ru,Huang Zhi-Tang,Zheng Qi-Yu

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference54 articles.

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3. Chemistry of Cyclotriveratrylene. I. Formation of Cyclotriveratrylene from Veratrylamine N-Tosylates

4. Medium-sized cyclophanes. Part XIV. An aromatic displacement reaction in veratrylic compounds. Attempted nitration and halogenation of cyclotriveratrylene (10,15-dihydro-2,3,7,8,12,13-hexamethoxy-5H-tri-benzo[a,d,g]cyclononene)

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1. Synthetic progress of CTVs with different numbers of substituents on aromatic units;Tetrahedron Letters;2022-08

2. Hemicryptophane Cages with a C1-Symmetric Cyclotriveratrylene Unit;The Journal of Organic Chemistry;2021-10-01

3. Controlled Access to C 1 ‐Symmetrical Cyclotriveratrylenes (CTVs) by Using a Sequential Barluenga Boronic Coupling (BBC) Approach;Advanced Synthesis & Catalysis;2021-07-09

4. Cyclotriveratrylene-tethered trinuclear palladium(ii)–NHC complexes; reversal of site selectivity in Suzuki–Miyaura reactions;Dalton Transactions;2019

5. Enantiopure C1-Cyclotriveratrylene with a Reversed Spatial Arrangement of the Substituents;Organic Letters;2018-12-14