Synthesis of Five-, Six-, and Seven-Membered Heterocycles by Intramolecular Ring Opening Reactions of 3-Oxetanol Derivatives-Reference-Cited by-同舟云学术

Synthesis of Five-, Six-, and Seven-Membered Heterocycles by Intramolecular Ring Opening Reactions of 3-Oxetanol Derivatives

Published:1998-02-20 Issue:6 Volume:63 Page:1910-1918
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Bach Thorsten¹,Kather Kristian¹,Krämer Oliver¹

Affiliation:

1. Fachbereich Chemie, Philipps-Universität Marburg, D-35032 Marburg, Germany, and Organisch-Chemisches Institut, Universität Münster, D-48149 Münster, Germany

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo971866z

Reference27 articles.

1. 1,3-Allylic Strain as a Control Element in the Paternò−Büchi Reaction of Chiral Silyl Enol Ethers: Synthesis of Diastereomerically Pure Oxetanes Containing Four Contiguous Stereogenic Centers

2. Reviews: (a) Kropf, H.; Thiem, J.; Nimz, H. InMethoden derOrganischen Chemie (Houben-Weyl), 4th ed.; Kropf, H., Ed.; Thieme: Stuttgart, 1979; Vol. VI/1a, p 338. (b) Lewars, E. G. InComprehensiveHeterocyclic Chemistry; Katritzky, A. R., Ed.; Pergamon Press: Oxford 1984; Vol. 7, p 96.

3. Diastereomerically Pure 3‐(Silyloxy)oxetanes by a Selective Paternò‐Büchi Reaction

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