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Asymmetric Allylation Catalyzed by Chiral Phosphoric Acids: Stereoselective Synthesis of Tertiary Alcohols and a Reagent‐Based Switch in Stereopreference
Author(s) -
Lazzarotto Mattia,
Hartmann Peter,
Pletz Jakob,
Belaj Ferdinand,
Kroutil Wolfgang,
Payer Stefan E.,
Fuchs Michael
Publication year - 2021
Publication title -
advanced synthesis and catalysis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.541
H-Index - 155
eISSN - 1615-4169
pISSN - 1615-4150
DOI - 10.1002/adsc.202100037
Subject(s) - stereocenter , chemistry , reagent , stereoselectivity , catalysis , enantioselective synthesis , tertiary alcohols , organic chemistry , zinc , substrate (aquarium) , asymmetric induction , combinatorial chemistry , oceanography , geology
Abstract The substrate scope of the asymmetric allylation with zinc organyls catalyzed by 3,3‐bis(2,4,6‐triisopropylphenyl)‐1,1‐binaphthyl‐2,2‐diyl hydrogenphosphate (TRIP) has been extended to non‐cyclic ester organozinc reagents and ketones. Tertiary chiral alcohols are obtained with ee's up to 94% and two stereogenic centers can be created. Compared to the previous lactone reagent the stereopreference switches almost completely, proving the fact that the nature of the organometallic compound is of immense importance for the asymmetry of the product.