Theoretical Study of the Mechanism of the Formation of 3-Unsubstituted 4,4-Disubstituted β-Lactams by Silver-Induced Ring Expansion of Alkoxycyclopropylamines: A New Synthetic Route to 4-Alkoxycarbonyl-4-alkyl-2-azetidinones-Reference-Cited by-同舟云学术

Theoretical Study of the Mechanism of the Formation of 3-Unsubstituted 4,4-Disubstituted β-Lactams by Silver-Induced Ring Expansion of Alkoxycyclopropylamines: A New Synthetic Route to 4-Alkoxycarbonyl-4-alkyl-2-azetidinones

Published:2003-07-31 Issue:17 Volume:68 Page:6685-6689
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Campomanes Pablo¹,Menéndez M. Isabel¹,Sordo Tomás L.¹

Affiliation:

1. Departamento de Química Física y Analítica, Facultad de Química, Universidad de Oviedo, C/Julián Clavería, 8, 33006 Oviedo, Principado de Asturias, Spain

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo034803r

Reference37 articles.

1. O-Sulfated .beta.-lactam hydroxamic acids (monosulfactams). Novel monocyclic .beta.-lactam antibiotics of synthetic origin

2. Enantiospecific and diastereoselective synthesis of 4,4-disubstituted-3-amino-2-azetidinones, starting from D-serine

3. Chemistry of cyclopropanones. VI. New synthesis of .beta.-lactams

Cited by 12 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. Enantioselective Synthesis of Cyclopropanone Equivalents and Application to the Formation of Chiral β‐Lactams;Angewandte Chemie International Edition;2020-08-18

2. Enantioselective Synthesis of Cyclopropanone Equivalents and Application to the Formation of Chiral β‐Lactams;Angewandte Chemie;2020-08-18

3. Solutions 151 – 200;Strategies and Solutions to Advanced Organic Reaction Mechanisms;2019

4. 3,3-gem-Difluorinated-β-lactams: synthesis pathways and applications;Tetrahedron;2013-05

5. Synthetic Applications of Nitrenium Ions;Nitrenes and Nitrenium Ions;2013-04-09