N-Tosylcarboxamide in C–H Functionalization: More than a Simple Directing Group
Abstract
:1. Introduction
2. C–H Functionalization Using N-Tosylcarboxamide as Directing Group
2.1. Alkenylation
2.2. Alkoxylation
2.3. Halogenation
2.4. Arylation
3. Access to Six-Membered Rings through C–H Functionalization and Subsequent Transformation of Tosylbenzamides
3.1. Sequential Approach
3.2. One-Pot Sequence
4. Access to Five-Membered Rings through C–H Functionalization and Subsequent Transformation of Tosylbenzamides
4.1. Fluorenones
4.2. Isoindolinones
4.3. Naphthalene-Fused Isoindolinones
5. Conclusions
Author Contributions
Funding
Conflicts of Interest
References
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Large, B.; Terrasson, V.; Prim, D. N-Tosylcarboxamide in C–H Functionalization: More than a Simple Directing Group. Processes 2020, 8, 981. https://doi.org/10.3390/pr8080981
Large B, Terrasson V, Prim D. N-Tosylcarboxamide in C–H Functionalization: More than a Simple Directing Group. Processes. 2020; 8(8):981. https://doi.org/10.3390/pr8080981
Chicago/Turabian StyleLarge, Benjamin, Vincent Terrasson, and Damien Prim. 2020. "N-Tosylcarboxamide in C–H Functionalization: More than a Simple Directing Group" Processes 8, no. 8: 981. https://doi.org/10.3390/pr8080981