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Recent Syntheses and Reactions of Cyclic Imidic Esters

Seeliger, W., Aufderhaar, E., Diepers, W., Feinauer, R., Nehring, R., Thier, W., Hellmann, H.·1966·Angewandte Chemie International Edition in English

Abstract

Δ 2‐Oxazolines and 4H‐5,6‐dihydrooxazines are readily obtainable from carboxylic acids and 2‐ or 3‐amino alcohols by gas‐phase dehydration, and 4H‐dihydrooxazines can also be obtained by condensation of N‐(hydroxymethyl) carboxamides with olefins. These cyclic imidic esters undergo reactions in which the ring is cleaved; these reactions include a new type of polymerization. The behavior of alkyl groups in position 2 and the cyclodditions in the 2,3‐position also have been studied. Reactions in side chains on position 2 and addition experiments on the sulfur analogues of the cyclic imidic esters are also reported. A table shows the principal infrared bands of substituted Δ 2‐oxazolines.

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Metadata

Authors
Seeliger, W., Aufderhaar, E., Diepers, W., Feinauer, R., Nehring, R., Thier, W., & Hellmann, H.
Venue
Angewandte Chemie International Edition in English
Publisher
Wiley
Published
1966-10
Volume
5
Issue
10
Pages
875-888
ISSN
0570-0833 (ISSN-L)
OpenAlex
W2005674807
Cited by
277
References
0
FWCI
6.26
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Recent Syntheses and Reactions of Cyclic Imidic Esters. https://app.cochat.ai/papers/10.1002/anie.196608751
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Seeliger, W., Aufderhaar, E., Diepers, W., Feinauer, R., Nehring, R., Thier, W., & Hellmann, H. (1966). Recent Syntheses and Reactions of Cyclic Imidic Esters. Angewandte Chemie International Edition in English. https://doi.org/10.1002/anie.196608751

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