Abstract
A new solid-phase synthesis of pyrrolizidine nucleus related to hyacinthacine core using L-proline as the starting material is reported. The final step is a new approach with a cyclization-cleave strategy, which releases the product from the resin in good yields under Baylis-Hillman conditions.
Keywords: Hyacinthacine core, solid-phase organic synthesis, L-Proline, enaminoester, Baylis-Hillman reaction
Letters in Organic Chemistry
Title: New Solid-Phase Approach to Synthesize a Hyacinthacine Core Using the L-Proline as a Building Block
Volume: 6 Issue: 1
Author(s): Monica O. Duarte, Guilherme Stedele, Mariane Pazinatto, Eduardo R. de Oliveira and Vera L. Eifler-Lima
Affiliation:
Keywords: Hyacinthacine core, solid-phase organic synthesis, L-Proline, enaminoester, Baylis-Hillman reaction
Abstract: A new solid-phase synthesis of pyrrolizidine nucleus related to hyacinthacine core using L-proline as the starting material is reported. The final step is a new approach with a cyclization-cleave strategy, which releases the product from the resin in good yields under Baylis-Hillman conditions.
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Cite this article as:
Duarte O. Monica, Stedele Guilherme, Pazinatto Mariane, de Oliveira R. Eduardo and Eifler-Lima L. Vera, New Solid-Phase Approach to Synthesize a Hyacinthacine Core Using the L-Proline as a Building Block, Letters in Organic Chemistry 2009; 6 (1) . https://dx.doi.org/10.2174/157017809787003241
DOI https://dx.doi.org/10.2174/157017809787003241 |
Print ISSN 1570-1786 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6255 |
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