PhI(OAc)2-Promoted Rearrangement of the Hydroxyl Group: Ring Expansion of 4-Hydroxy-2-cyclobutenone to 2(5H)-Furanone in Comparison with Ring Cleavage of the α-Hydroxycycloalkanone to the ω-Formyl Ester-Reference-Cited by-同舟云学术

PhI(OAc)2-Promoted Rearrangement of the Hydroxyl Group: Ring Expansion of 4-Hydroxy-2-cyclobutenone to 2(5H)-Furanone in Comparison with Ring Cleavage of the α-Hydroxycycloalkanone to the ω-Formyl Ester

Published:1999-11-19 Issue:25 Volume:64 Page:8995-9000
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Ohno Masatomi¹,Oguri Isamu²,Eguchi Shoji²

Affiliation:

1. Department of Materials Science and Engineering, Toyota Technological Institute, 2−12−1 Hisakata, Tempaku, Nagoya 468-8511, Japan

2. Department of Applied Chemistry, Graduate School of Engineering, Nagoya University, Chikusa, Nagoya 464-8603, Japan

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo990704v

Reference30 articles.

1. Reaktionen von Quadratsäure und Quadratsäure-Derivaten

2. Cyclobutenediones as precursors to quinones and cyclopentenones

3. Reactivity of organo lithium reagents on dimethyl squarate : a 1,2-addition process leading to new 2-hydroxy-3,4 dimethoxy 3-cyclobutenone

4. Synthesis of 4-substituted-3-alkoxy-3-cyclobutene-1,2-diones

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