Highly Diastereoselective Baldwin Rearrangement of Isoxazolines into cis-Acylaziridines-Reference-Cited by-同舟云学术

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Highly Diastereoselective Baldwin Rearrangement of Isoxazolines into cis-Acylaziridines

Published:2010-08-03 Issue:17 Volume:75 Page:6050-6053
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Gayon Eric¹,Debleds Olivier¹,Nicouleau Marie¹,Lamaty Frederic²,van der Lee Arie³,Vrancken Emmanuel¹,Campagne Jean-Marc¹

Affiliation:

1. Institut Charles Gerhardt (ICGM), UMR 5253 CNRS-UM2-UM1-ENSCM, 8 rue de l’Ecole Normale, 34296 Montpellier Cedex 5, France

2. Institut des Biomolécules Max Mousseron (IBMM), UMR 5247 CNRS-UM1-UM2, Place E. Bataillon, 34095 Montpellier Cedex 5, France

3. Institut Européen des Membranes, UMR-CNRS 5635, Place E. Bataillon, 34085 Montpellier Cedex 5, France

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo101273d

Reference38 articles.

1. Valence rearrangement of hetero systems. The 4-isoxazolines

2. .DELTA.4-Isoxazolines (2,3-dihydroisoxazoles)

3. 4‐Isoxazolines: Scaffolds for Organic Synthesis

4. Addition of nitronic esters to alkynes. Formation under kinetic control of aziridine invertomers. Study of the transposition of 4-isoxazolines to acylaziridines

5. Skeletal rearrangement of nitrogen, oxygen-heterocycles. The isoxazolinone to aziridine transformation induced by lithium aluminum hydride

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2. Development of a Continuous Flow Baldwin Rearrangement Process and Its Comparison to Traditional Batch Mode;Organic Process Research & Development;2023-09-11

3. Non-Aziridination Approaches to 3-Arylaziridine-2-carboxylic Acid Derivatives and 3-Aryl-(aziridin-2-yl)ketones;International Journal of Molecular Sciences;2022-05-25

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