Intramolecular Cyclization with Nitrenium Ions Generated by Treatment of N-Acylaminophthalimides with Hypervalent Iodine Compounds: Formation of Lactams and Spiro-Fused Lactams-Reference-Cited by-同舟云学术

Intramolecular Cyclization with Nitrenium Ions Generated by Treatment of N-Acylaminophthalimides with Hypervalent Iodine Compounds: Formation of Lactams and Spiro-Fused Lactams

Published:2003-07-26 Issue:17 Volume:68 Page:6739-6744
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Kikugawa Yasuo¹,Nagashima Akira¹,Sakamoto Takeshi¹,Miyazawa Etsuko¹,Shiiya Megumi¹

Affiliation:

1. Faculty of Pharmaceutical Sciences, Josai University, 1-1 Keyakidai, Sakado, Saitama 350-0295, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo0347009

Reference30 articles.

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2. (b) Abramovitch, R. A.; Jeyaraman, R. InAzides and Nitrenes: Reactivity and Utility; Scriven, E. F. V., Ed.; Academic Press: New York, 1984; pp 297−357.

3. MNDO molecular orbital study of nitrenium ions derived from carcinogenic aromatic amines and amides

4. N-alkoxy-n-acylnitrenium ions in intramolecular aromatic addition reactions

5. MNDO properties of heteroatom and phenyl substituted nitrenium ions

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