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- W4242346436 abstract "AAA: Die asymmetrische allylische Alkylierung (AAA) trisubstituierter cyclischer Allylbromide mit Grignard-Reagentien ist katalytisch (2 Mol-% Ligand) und regioselektiv (SN2'/SN2=91:9 bis 100:0). Die quartären Kohlenstoffzentren werden mit guter bis hoher Enantioselektivität aufgebaut (e.r.=81.5:19.5 bis 96:4). As a service to our authors and readers, this journal provides supporting information supplied by the authors. Such materials are peer reviewed and may be re-organized for online delivery, but are not copy-edited or typeset. Technical support issues arising from supporting information (other than missing files) should be addressed to the authors. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article." @default.
- W4242346436 created "2022-05-12" @default.
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- W4242346436 date "2013-11-07" @default.
- W4242346436 modified "2023-10-18" @default.
- W4242346436 title "Copper-Free Asymmetric Allylic Alkylation of Trisubstituted Cyclic Allyl Bromides Using Grignard Reagents" @default.
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- W4242346436 doi "https://doi.org/10.1002/ange.201307591" @default.
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