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1 Ergebnisse
1
Simplified Modular Access to Enantiopure 1,2-Aminoalcohols ..:
Jiawei Sun
;
Hirofumi Endo
;
Megan A. Emmanuel
...
doi:10.1021/jacs.3c14119.s001. , 1753
Link:
https://doi.org/10.1021/jacs.3c14119.s001
RT Journal T1
Simplified Modular Access to Enantiopure 1,2-Aminoalcohols via Ni-Electrocatalytic Decarboxylative Arylation
UL https://suche.suub.uni-bremen.de/peid=base-ftgriffithunifig:oai:figshare.com:article_25270690&Exemplar=1&LAN=DE A1 Jiawei Sun A1 Hirofumi Endo A1 Megan A. Emmanuel A1 Martins S. Oderinde A1 Yu Kawamata A1 Phil S. Baran YR 1753 K1 Biochemistry K1 Genetics K1 Pharmacology K1 Biotechnology K1 Evolutionary Biology K1 Mental Health K1 Environmental Sciences not elsewhere classified K1 Chemical Sciences not elsewhere classified K1 thereby dramatically simplifying K1 substituted chiral aminoalcohols K1 simple chiral oxazolidine K1 motif involve multiple K1 high stereochemical control K1 functional group manipulations K1 electrocatalytic decarboxylative arylation K1 based carboxylic acid K1 medicinally important compounds K1 simplified modular access K1 aminoalcohols via ni K1 bioactive compounds K1 study reveals K1 step reactions K1 scalable coupling K1 readily transformed K1 enantiopure 1 K1 conventional strategies K1 avoiding protecting JF doi:10.1021/jacs.3c14119.s001 LK http://dx.doi.org/https://doi.org/10.1021/jacs.3c14119.s001 DO https://doi.org/10.1021/jacs.3c14119.s001 SF ELIB - SuUB Bremen
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