Basicity-Tuned Reactivity: diaza-[1,2]-Wittig versus diaza-[1,3]-Wittig Rearrangements of 3,4-Dihydro-2H-1,2,3-benzothiadiazine 1,1-Dioxides-Reference-Cited by-同舟云学术

Basicity-Tuned Reactivity: diaza-[1,2]-Wittig versus diaza-[1,3]-Wittig Rearrangements of 3,4-Dihydro-2H-1,2,3-benzothiadiazine 1,1-Dioxides

Published:2020-12-31 Issue:2 Volume:86 Page:1685-1700
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Gyűjtő Imre¹²,Porcs-Makkay Márta¹,Szabó Gergő²,Kelemen Zsolt²^ORCID,Pusztai Gyöngyvér¹,Tóth Gábor¹²,Dancsó András¹^ORCID,Halász Judit¹,Simig Gyula¹,Volk Balázs¹^ORCID,Nyulászi László²^ORCID

Affiliation:

1. Directorate of Drug Substance Development, Egis Pharmaceuticals Plc., P.O. Box 100, H-1475 Budapest, Hungary

2. Department of Inorganic and Analytical Chemistry, Budapest University of Technology and Economics, and MTA-BME Computation Driven Chemistry Research Group, Szt. Gellért tér 4, H-1111 Budapest, Hungary

Funder

Magyar Tudom?nyos Akad?mia

Nemzeti Kutat?si Fejleszt?si ?s Innov?ci?s Hivatal

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

http://pubs.acs.org/doi/pdf/10.1021/acs.joc.0c02512

Reference64 articles.

1. 3.20 Nitrogen- and Sulfur-Based Stevens and Related Rearrangements

2. The mechanism of the Stevens and Sommelet−Hauser Rearrangements. A Theoretical Study

3. Dynamics and a Unified Understanding of Competitive [2,3]- and [1,2]-Sigmatropic Rearrangements Based on a Study of Ammonium Ylides

4. 3.21 The Wittig Rearrangement

5. Applications of the Wittig-Still Rearrangement in Organic Synthesis

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1. Dearomative spiroannulation of indoles enabled by the diaza-[1,2]-Wittig rearrangement;Organic Chemistry Frontiers;2024

2. Effect of aromatic substituents on the outcome of base-induced rearrangements of 3-acetyl-2,4-dimethyl-3,4-dihydro-2H-1,2,3-benzothiadiazine 1,1-dioxides;Tetrahedron;2023-07