Sceptrin - Enantioselective Synthesis of a Tetrasubstituted all-trans Cyclobutane Key Intermediate-Reference-Cited by-同舟云学术

Sceptrin - Enantioselective Synthesis of a Tetrasubstituted all-trans Cyclobutane Key Intermediate

Published:2017-08-21 Issue:31 Volume:2017 Page:4566-4571
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur. J. Org. Chem.

Author:

Barra Lena¹,Dickschat Jeroen S.¹^ORCID

Affiliation:

1. Kekulé-Institute of Organic Chemistry and Biochemistry; Rheinische Friedrich Wilhelms University of Bonn; Gerhard-Domagk-Straße 1 53121 Bonn Germany

Funder

Deutsche Forschungsgemeinschaft

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ejoc.201700882/fullpdf

Reference30 articles.

1. How cyclobutanes are assembled in nature – insights from quantum chemistry

2. Attractive natural products with strained cyclopropane and/or cyclobutane ring systems

3. Naturally occurring bioactive Cyclobutane-containing (CBC) alkaloids in fungi, fungal endophytes, and plants

4. Anisucoumaramide, a Bioactive Coumarin from Clausena anisum-olens

5. Sceptrin, an antimicrobial agent from the sponge Agelas sceptrum

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