1,3-Diaza-Claisen Rearrangements of Vinyl Pyrrolidines Tethered to In Situ Generated Carbodiimides Afford Ring-Expanded [9,5]- and [9,6]-Bicyclic Guanidines-Reference-Cited by-同舟云学术

1,3-Diaza-Claisen Rearrangements of Vinyl Pyrrolidines Tethered to In Situ Generated Carbodiimides Afford Ring-Expanded [9,5]- and [9,6]-Bicyclic Guanidines

Published:2023-02-17 Issue:5 Volume:88 Page:2851-2868
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Watanabe Teruki¹,Pisano Joseph¹,Mangione Caroline¹,Madalengoitia José S.¹^ORCID

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.2c02524

Reference48 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. Intramolecular Formation of Zwitterionic Intermediates in 1,3-Diaza-Claisen Rearrangements

5. Broadening the Scope of the Zwitterionic 1,3-Diaza-Claisen Rearrangement through a Tethering Strategy

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. Crystal structures of sulfonamide protected bicyclic guanidines: (S)-8-{[(tert-butyldimethylsilyl)oxy]methyl}-1-[(2,2,4,6,7-pentamethyl-2,3-dihydrobenzofuran-5-yl)sulfonyl]-1,3,4,6,7,8-hexahydro-2H-pyrimido[1,2-a]pyrimidin-1-ium trifluoromethanesulfonate and (S)-8-(iodomethyl)-1-tosyl-1,3,4,6,7,8-hexahydro-2H-pyrimido[1,2-a]pyrimidin-1-ium iodide;Acta Crystallographica Section E Crystallographic Communications;2024-02-20

2. One-pot four-component synthesis of novel isothiourea-ethylene-tethered-piperazine derivatives;RSC Advances;2023