Highly Diastereoselective Crown Ether Catalyzed Arylogous Michael Reaction of 3-Aryl Phthalides-Reference-Cited by-同舟云学术

Highly Diastereoselective Crown Ether Catalyzed Arylogous Michael Reaction of 3-Aryl Phthalides

Published:2017-08-09 Issue:16 Volume:19 Page:4383-4386
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Sicignano Marina¹,Dentoni Litta Antonella¹,Schettini Rosaria¹,De Riccardis Francesco¹^ORCID,Pierri Giovanni¹,Tedesco Consiglia¹,Izzo Irene¹^ORCID,Della Sala Giorgio¹^ORCID

Affiliation:

1. Dipartimento di Chimica e Biologia “A. Zambelli”, Università degli Studi di Salerno, Via Giovanni Paolo II 132, 84084 Fisciano, SA, Italy

Funder

European Regional Development Fund

Regione Campania

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.7b02113

Reference56 articles.

1. aDevon, T. K.; Scott, A. I.Handbook of Naturally Occurring Compounds, Vol.1;Academic Press:New York, 1975; pp249–264.

2. bLin, G.; Chan, S. S.K.; Chung, H.S.; Li, S.L.InStudies in Natural Products Chemistry: Bioactive Natural Products, Vol.32 (Part L);Atta-ur-Rahman, Ed.Elsevier,Amsterdam, 2005; pp611–669.

3. The Structural Diversity of Phthalides from the Apiaceae

4. Antibacterial Polyketides from the Jellyfish-Derived Fungus Paecilomyces variotii

5. Recent pharmacological studies on natural products in China

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