✦ LIBER ✦

5-Amino-4,5-dihydroisoxazoles. Part II . Reactions of 5-amino-3-aryl-4-methylene-4,5-dihydroisoxazoles with Nucleophiles

✍ Scribed by Donato Pocar; Luisa Maria Rossi; Franca Scorca; Pasqualina Trimarco

Book ID: 112126068
Publisher: Journal of Heterocyclic Chemistry
Year: 1980
Tongue: English
Weight: 272 KB
Volume: 17
Category: Article
ISSN: 0022-152X
DOI: 10.1002/jhet.5570170509

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

5-Amino-4,5-dihydroisoxazoles. Part I. 5

5-Amino-4,5-dihydroisoxazoles. Part I. 5-Amino-3-aryl-4-methylene-4,5-dihydroisoxazoles and 4-aminomethyl-3-arylisoxazoles from 5-amino-4-aminomethyl-3-aryl-4,5-dihydroisoxazoles

✍ Donato Pocar; Luisa Maria Rossi; Pasqualina Trimarco; Luciano Vago 📂 Article 📅 1980 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 323 KB

Synthesis of 3-aryl-5-diethoxyphosphoryl

Synthesis of 3-aryl-5-diethoxyphosphorylethyne-4,5-dihydroisoxazoles

✍ V. K. Brel’ 📂 Article 📅 2012 🏛 Springer US 🌐 English ⚖ 297 KB

Reaction of 3,5-Disubstituted 4,5-Dihydr

Reaction of 3,5-Disubstituted 4,5-Dihydroisoxazoles with Hexacarbonylmolybdenum

✍ E. V. Koroleva; Ya. M. Katok; F. A. Lakhvich 📂 Article 📅 2004 🏛 SP MAIK Nauka/Interperiodica 🌐 English ⚖ 82 KB

Reaction of 3,5-Disubstituted 4,5-Dihydr

Reaction of 3,5-Disubstituted 4,5-Dihydroisoxazoles with Hexacarbonylmolybdenum.

✍ E. V. Koroleva; Ya. M. Katok; F. A. Lakhvich 📂 Article 📅 2005 🏛 John Wiley and Sons ⚖ 20 KB

A Library of 3-Aryl-4,5-dihydroisoxazole

A Library of 3-Aryl-4,5-dihydroisoxazole-5-carboxamides

✍ Jeddeloh, Melissa R.; Holden, Jason B.; Nouri, Dustin H.; Kurth, Mark J. 📂 Article 📅 2007 🏛 American Chemical Society 🌐 English ⚖ 740 KB

4,5-dihydroisoxazoles, IX. Reactions of

4,5-dihydroisoxazoles, IX. Reactions of 3-aryl-4,5-dihydro-4-methylene-5-morpholinoisoxazoles with 2,4-diaryl-5(4H)-oxazolones: A new synthesis of tetrahydro-6-oxo-3-pyridinecarbaldehydes

✍ Erba, Emanuela ;Pocar, Donato 📂 Article 📅 1990 🏛 John Wiley and Sons 🌐 English ⚖ 277 KB

## Abstract The 5(4__H__)‐oxazolones 1a–e react with 5‐morpholinoisoxazoles 2a–b to afford the 4‐[(4‐isoxazolyl)methyl]‐5(4__H__)‐oxazolones 3a–g. Compounds 3 are hydrogenated with Pd/C in dioxane to yield the corresponding 1,4,5,6‐tetrahydro‐6‐oxo‐3‐pyridinecarbaldehydes 6a–d.