Temporäre Bildung eines Cyclopropyl-Oxocarbeniumions ermöglicht eine außerordentlich diastereoselektive Cycloaddition von Donor-Akzeptor-Cyclopropanen-Reference-Cited by-同舟云学术

Temporäre Bildung eines Cyclopropyl-Oxocarbeniumions ermöglicht eine außerordentlich diastereoselektive Cycloaddition von Donor-Akzeptor-Cyclopropanen

Published:2016-04-21 Issue:23 Volume:128 Page:6892-6895
ISSN:0044-8249
Container-title:Angewandte Chemie
language:en
Short-container-title:Angew. Chem.

Author:

Sabbatani Juliette¹,Maulide Nuno¹

Affiliation:

1. Fakultät für Chemie, Institut für Organische Chemie; Universität Wien; Währinger Straße 38 1090 Wien Österreich

Funder

Deutschen Forschungsgemeinschaft

Publisher

Wiley

Subject

General Medicine

Reference49 articles.

1. Recent advances in the stereoselective synthesis of tetrahydrofurans

2. Lewis-acid-promoted additions of carbonyl compounds to donor-acceptor substituted cyclopropanes: a new synthesis of 2,3-dihydrofurane derivatives

3. Total synthesis of aromatic steroids

4. A titanoxycyclopropane as intermediate in a highly stereoselective homoaldol type addition syntheses of -substituted tetrahydrofuran derivatives

Cited by 39 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. A Widely Applicable and Versatile Method for the Ring‐Opening 1,3‐Carbocarbonation of Donor‐Acceptor Cyclopropanes;Chemistry – A European Journal;2023-02-28

2. Donor‐Acceptor Cyclopropanes: Activation Enabled by a Single, Vinylogous Acceptor;Angewandte Chemie International Edition;2022-11-30

3. Donor‐Acceptor Cyclopropanes: Activation Enabled by a Single, Vinylogous Acceptor;Angewandte Chemie;2022-11-30

4. From Enantioenriched Donor‐Acceptor Cyclopropylcarbinols to Axially Chiral Arylnaphthalenes through Aryldihydronaphthalenes: Central‐to‐Axial Chirality Exchange;European Journal of Organic Chemistry;2021-11-23

5. Cycloadditions of Donor–Acceptor Cyclopropanes and ‐butanes using S=N‐Containing Reagents: Access to Cyclic Sulfinamides, Sulfonamides, and Sulfinamidines;Angewandte Chemie International Edition;2021-10-29