Broadening the Scope of the Zwitterionic 1,3-Diaza-Claisen Rearrangement through a Tethering Strategy
Author:
Affiliation:
1. Department of Chemistry, University of Vermont, Burlington, Vermont 05405, United States
Funder
Division of Chemistry
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.joc.1c00667
Reference44 articles.
1. A 1,3-Diaza-Claisen Rearrangement that Affords Guanidines
2. Structure–Reactivity Relationships of Zwitterionic 1,3-Diaza-Claisen Rearrangements
3. Optimization of methods for the generation of carbodiimides for zwitterionic 1,3-diaza-Claisen rearrangements
4. Amino-Claisen rearrangements of N-vinylisoquinuclidines in novel approaches to the synthesis of hydroisoquinolines and hydrophenanthridines
5. Formal total synthesis of deserpidine demonstrating a versatile amino-Claisen rearrangement/Wenkert cyclization strategy for the preparation of functionalized yohimbane ring systems
Cited by 2 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. 1,3-Diaza-Claisen Rearrangements of Vinyl Pyrrolidines Tethered to In Situ Generated Carbodiimides Afford Ring-Expanded [9,5]- and [9,6]-Bicyclic Guanidines;The Journal of Organic Chemistry;2023-02-17
2. Stereoselective synthesis of vinylphosphonates through aromatic aza-Claisen rearrangement of α-aminophosphonates;Chemical Communications;2023
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