Enantioselective Synthesis of Xanthatin-Reference-Cited by-同舟云学术

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Enantioselective Synthesis of Xanthatin

Published:2014-05-13 Issue:25 Volume:20 Page:7613-7615
ISSN:0947-6539
Container-title:Chemistry – A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Bergmann Andreas¹,Reiser Oliver¹²

Affiliation:

1. Institut für Organische Chemie, Universität Regensburg, Universitätsstrasse 31, 93053 Regensburg (Germany), Fax: (+49) 941‐943‐4121

2. Current address: Department of Chemistry, Tokyo Institute of Technology, 2‐12‐1 O‐okayama, Meguro‐ku, Tokyo 152‐8551 (Japan)

Funder

Deutsche Forschungsgemeinschaft

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/chem.201402735

Reference48 articles.

1.

2. Systematic implications of the sesquiterpene lactones in the “strumarium” morphological complex (Xanthium strumarium, Asteraceae) of Europe, Asia and Africa

3. Xanthane sesquiterpenoids: structure, synthesis and biological activity

4.

5. Biological Activities of Xanthatin from Xanthium strumarium Leaves

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1. Synthesis of natural products by photochemistry;Green Approaches in Medicinal Chemistry for Sustainable Drug Design;2024

2. Heterocycles from Cyclopropanation of Five-Membered Heteroarenes;Topics in Heterocyclic Chemistry;2023

3. Natural product-based semisynthesis and biological evaluation of thiol/amino-Michael adducts of xanthatin derived from Xanthium strumarium as potential pesticidal agents;Bioorganic Chemistry;2020-04

4. Advances in the Total Synthesis of Xanthanolide‐Type Sesquiterpenoids;Chemistry – An Asian Journal;2019-04-16

5. An Approach to the 9-Oxo-10-oxabicyclo[5.3.0]dec-2-ene Core of the Guaianolide and Pseudoguaianolide Sesquiterpenes via a Domino Electrocyclic Ring-Opening/Carboxylic Acid Trapping of a gem-Dibromocyclopropane;The Journal of Organic Chemistry;2018-10-10

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