Please use this identifier to cite or link to this item: http://dx.doi.org/10.14279/depositonce-9654
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Main Title: Copper‐Catalyzed Enantio‐ and Diastereoselective Addition of Silicon Nucleophiles to 3,3‐Disubstituted Cyclopropenes
Author(s): Zhang, Liangliang
Oestreich, Martin
Type: Article
Language Code: en
Abstract: A highly stereocontrolled syn‐addition of silicon nucleophiles across cyclopropenes with two different geminal substituents at C3 is reported. Diastereomeric ratios are excellent throughout (d.r.≥98:2) and enantiomeric excesses usually higher than 90 %, even reaching 99 %. This copper‐catalyzed C−Si bond formation closes the gap of the direct synthesis of α‐chiral cyclopropylsilanes.
URI: https://depositonce.tu-berlin.de/handle/11303/10759
http://dx.doi.org/10.14279/depositonce-9654
Issue Date: 22-Oct-2019
Date Available: 13-Feb-2020
DDC Class: 540 Chemie und zugeordnete Wissenschaften
660 Chemische Verfahrenstechnik
Subject(s): asymmetric catalysis
boron
copper
silicon
strained molecules
Sponsor/Funder: TU Berlin, Open-Access-Mittel - 2019
License: https://creativecommons.org/licenses/by-nc/4.0/
Journal Title: Chemistry – A European Journal
Publisher: Wiley
Publisher Place: Weinheim
Volume: 25
Issue: 63
Publisher DOI: 10.1002/chem.201904272
Page Start: 14304
Page End: 14307
EISSN: 1521-3765
ISSN: 0947-6539
Appears in Collections:FG Organische Chemie / Synthese und Katalyse » Publications

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