Regio and diastereoselective multicomponent 1,3-dipolar cycloadditions between prolinate hydrochlorides, aldehydes and dipolarophiles for the direct synthesis of pyrrolizidines-Reference-Cited by-同舟云学术

Regio and diastereoselective multicomponent 1,3-dipolar cycloadditions between prolinate hydrochlorides, aldehydes and dipolarophiles for the direct synthesis of pyrrolizidines

Published:2015-12 Issue:52 Volume:71 Page:9645-9661
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Mancebo-Aracil Juan,Nájera Carmen,Castelló Luis M.,Sansano José M.,Larrañaga Olatz,de Cózar Abel,Cossío Fernando P.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference96 articles.

1. As recent reviews concerning this topic, see

2. The evolution of pyrrolizidine alkaloid biosynthesis and diversity in the Senecioneae

3. Defensive properties of pyrrolizidine alkaloids against microorganisms

4. Polyhydroxylated alkaloids — natural occurrence and therapeutic applications

5. For very recent examples, see

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