Straightforward Enantioselective Access to γ-Butyrolactones Bearing an All-Carbon β-Quaternary Stereocenter-Reference-Cited by-同舟云学术

Straightforward Enantioselective Access to γ-Butyrolactones Bearing an All-Carbon β-Quaternary Stereocenter

Published:2014-09-09 Issue:18 Volume:16 Page:4746-4749
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Meninno Sara¹,Fuoco Tiziana¹,Tedesco Consiglia¹,Lattanzi Alessandra¹

Affiliation:

1. Dipartimento di Chimica e Biologia, Università di Salerno, Via Giovanni Paolo II, 84084 Fisciano, Italy

Funder

European Cooperation in Science and Technology

Ministero dell'Istruzione, dell'Università e della Ricerca

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol502148a

Reference62 articles.

1. aKoch, S. S. C.; Chamberlain, A. R.InEnantiomerically Pure γ-Butyrolactones in Natural Products Synthesis in Studies in Natural Products Chemistry;Atta-ur-Rahman, Ed.Elsevier Science:New York, 1995; Vol.16, pp687–725.

2. Synthetic approaches towards structurally diverse γ-butyrolactone natural-product-like compounds

3. Natural and synthetic α-methylenelactones and α-methylenelactams with anticancer potential

4. aMulzer, J.InComprehensive Organic Synthesis;Trost, B. M.; Fleming, I.; Winterfeldt, E., Eds.Pergamon:Oxford, 1991; Vol.6, pp323–380.

5. A Facile Synthesis of Chiral γ-Butyrolactones in Extremely High Enantioselectivity Mediated by Samarium(II) Iodide

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