Rearrangement of isoxazoline-5-spiro derivatives. Part 7. Thermal rearrangement of 4,5-dihydro and tetrahydroisoxazole-5-spirocyclobutanes to azepin-4-one derivatives-Reference-Cited by-同舟云学术

Rearrangement of isoxazoline-5-spiro derivatives. Part 7. Thermal rearrangement of 4,5-dihydro and tetrahydroisoxazole-5-spirocyclobutanes to azepin-4-one derivatives

Published:1992 Issue:25 Volume:48 Page:5283-5300
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Goti Andrea,Brandi Alberto,De Sarlo Francesco,Guarna Antonio

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference40 articles.

1. Rearrangement of nitrone cycloadducts to methylene cyclopropane. Synthesis of indolizidine and quinolizidine derivatives.

2. Rearrangement of isoxazoline-5-spiro derivatives. 1. Synthesis of 4,5-dihydroisoxazole-5-spirocyclopropanes and their rearrangement to 5,6-dihydro-4-pyridones

3. Rearrangement of isoxazoline-5-spiro derivatives. 2. Synthesis and rearrangement of tetrahydroisoxazole-5-spirocyclopropanes. Preparation of precursors of quinolizine, isoquinoline, and indole alkaloids

4. Rearrangement of isoxazoline-5-spiro derivatives. 5. Diastereofacial selectivity in the cycloaddition of substituted five-membered cyclic nitrones and methylenecyclopropanes. Stereoselective synthesis of 3,5-substituted indolizidinones

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