Chemo-, regio-, and stereoselectivity in 1,3-dipolar cycloaddition of piperine with nitrones. A cycloadditive route to aminoalcohols-Reference-Cited by-同舟云学术

Chemo-, regio-, and stereoselectivity in 1,3-dipolar cycloaddition of piperine with nitrones. A cycloadditive route to aminoalcohols

Published:2020 Issue:15 Volume:44 Page:6015-6025
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Wójtowicz-Rajchel Hanna¹²³⁴⁵^ORCID,Kaźmierczak Marcin¹²³⁴⁵^ORCID

Affiliation:

1. Faculty of Chemistry

2. Adam Mickiewicz University

3. Uniwersytetu Poznańskiego 8

4. 61-614 Poznań

5. Poland

Abstract

The chemoselective 1,3-dipolar cycloaddition between piperine and nitrones and further transformation of the cycloadducts to novel acyclic 1,3-amino alcohols.

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2020/NJ/C9NJ06442G

Reference57 articles.

1. Biosynthetic medicinal chemistry of natural product drugs

2. Natural and engineered biosynthesis of fluorinated natural products

3. Strategies to diversify natural products for drug discovery

4. Piper nigrum and Piperine: An Update

5. Piperine-mediated drug interactions and formulation strategy for piperine: recent advances and future perspectives

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