Construction of fully substituted carbon centers containing a heteroatom and a CF3 group via in situ generated p-quinone methides
Author:
Affiliation:
1. Division of Applied Chemistry
2. Institute of Engineering
3. Tokyo University of Agriculture and Technology
4. Koganei 184-8588
5. Japan
Abstract
Facile and practical construction of heteroatom as well as CF3-containing fully substituted carbon centers was realized by 1,6-conjugate additions of a variety of heteronucleophiles to in situ generated δ-CF3-δ-substituted p-quinone methides.
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2021/OB/D0OB02469D
Reference64 articles.
1. Recent Advances in the Catalytic Enantioselective Reactions of para -Quinone Methides
2. para -Quinone Methides as Acceptors in 1,6-Nucleophilic Conjugate Addition Reactions for the Synthesis of Structurally Diverse Molecules
3. Gold-catalyzed tandem reaction of 2-alkynylanilines followed by 1,6-conjugate addition to p-quinone methides: efficient access to unsymmetrical diarylindolylmethanes
4. Base-Mediated 1,6-Aza-Michael Addition of Heterocyclic Amines and Amides to para-Quinone Methides Leading to Meclizine-, Hydroxyzine- and Cetirizine-like Architectures
5. Synthesis of 2,4‐Diaryl‐1,3‐benzoxazines via FeCl 3 ‐Catalyzed Annulation of ortho ‐Hydroxyphenyl‐Substituted para ‐Quinone Methides with Imidates
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1. Construction of CF<sub>3</sub>-containing Tetrasubstituted Carbon Frameworks by Way of <i>p</i>-Quinone Methides;Journal of Synthetic Organic Chemistry, Japan;2023-03-01
2. Synthesis and synthetic applications of (4-hydroxyphenyl)perfluoroalkylmethanols;Tetrahedron;2022-01
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