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Catalytic stereoconvergent synthesis of homochiral β‑CF$_3$, β‑SCF$_3$, and β‑OCF$_3$ benzylic alcohols
ID Cotman, Andrej Emanuel (Author), ID Dub, Pavel A. (Author), ID Sterle, Maša (Author), ID Lozinšek, Matic (Author), ID Dernovšek, Jaka (Author), ID Zajec, Živa (Author), ID Zega, Anamarija (Author), ID Tomašič, Tihomir (Author), ID Cahard, Dominique (Author)

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Abstract
We describe an efficient catalytic strategy for enantio- and diastereoselective synthesis of homochiral β-CF$_3$, β-SCF$_3$, and β-OCF$_3$ benzylic alcohols. The approach is based on dynamic kinetic resolution (DKR) with Noyori−Ikariya asymmetric transfer hydrogenation leading to simultaneous construction of two contiguous stereogenic centers with up to 99.9% ee, up to 99.9:0.1 dr, and up to 99% isolated yield. The origin of the stereoselectivity and racemization mechanism of DKR is rationalized by density functional theory calculations. Applicability of the previously inaccessible chiral fluorinated alcohols obtained by this method in two directions is further demonstrated: As building blocks for pharmaceuticals, illustrated by the synthesis of heat shock protein 90 inhibitor with in vitro anticancer activity, and in particular, needle-shaped crystals of representative stereopure products that exhibit either elastic or plastic flexibility, which opens the door to functional materials based on mechanically responsive chiral molecular crystals.

Language:English
Keywords:adaptive crystals, asymmetric catalysis, density functional calculations, drug design, fluorine, hydrogenation, kinetic resolution, ruthenium, alcohols, catalysts, crystals, ketones, stereoselectivity
Work type:Article
Typology:1.01 - Original Scientific Article
Organization:FFA - Faculty of Pharmacy
Publication status:Published
Publication version:Version of Record
Year:2022
Number of pages:Str. 396−404
Numbering:Vol. 2, iss. 5
PID:20.500.12556/RUL-141984 This link opens in a new window
UDC:54
ISSN on article:2694-247X
DOI:10.1021/acsorginorgau.2c00019 This link opens in a new window
COBISS.SI-ID:111499267 This link opens in a new window
Publication date in RUL:13.10.2022
Views:1351
Downloads:240
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Record is a part of a journal

Title:ACS organic & inorganic Au
Shortened title:ACS org. inorg. Au
Publisher:American Chemical Society
ISSN:2694-247X
COBISS.SI-ID:103423491 This link opens in a new window

Licences

License:CC BY 4.0, Creative Commons Attribution 4.0 International
Link:http://creativecommons.org/licenses/by/4.0/
Description:This is the standard Creative Commons license that gives others maximum freedom to do what they want with the work as long as they credit the author.

Projects

Funder:ARRS - Slovenian Research Agency
Project number:P1-0208
Name:Farmacevtska kemija: načrtovanje, sinteza in vrednotenje učinkovin

Funder:ARRS - Slovenian Research Agency
Project number:Z1-2635
Name:Modularna asimetrična totalna sinteza biološko aktivnih naravnih produktov z več kiralnimi centri

Funder:ARRS - Slovenian Research Agency
Project number:J1-1717
Name:Razvoj novih zaviralcev Hsp90 s protitumornim delovanjem

Funder:Other - Other funder or multiple funders
Funding programme:Centre National de la Recherche Scientifique

Funder:Other - Other funder or multiple funders
Funding programme:Normandy University

Funder:ARRS - Slovenian Research Agency
Project number:BI-FR/22-23-PROTEUS-004

Funder:Other - Other funder or multiple funders
Funding programme:Los Alamos Laboratory Directed Research and Development

Funder:EC - European Commission
Funding programme:H2020
Project number:950625
Name:Challenging the Oxidation-State Limitations of the Periodic Table via High-Pressure Fluorine Chemistry
Acronym:HiPeR-F

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