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Rhodium-Catalyzed Asymmetric Addition to 4- or 5‑Carbonyl-c..:

Wen-Cong Li ; He Meng ; Jialin Ming.
doi:10.1021/acs.orglett.3c04281.s001. , 2024

Link: https://doi.org/10.1021/acs.orglett.3c04281.s001

RT Journal
T1 <Title>Rhodium-Catalyzed Asymmetric Addition to 4- or 5‑Carbonyl-cycloenones through Dynamic Kinetic Resolution: Enantioselective Synthesis of (−)-Cannabidiol</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftunivoxfordfig:oai:figshare.com:article_25225803&Exemplar=1&LAN=DE
				
A1 Wen-Cong Li
A1 He Meng
A1 Jialin Ming
A1 Shufeng Chen
YR 2024
K1 Biophysics
K1 Biochemistry
K1 Microbiology
K1 Molecular Biology
K1 Sociology
K1 Infectious Diseases
K1 Plant Biology
K1 Virology
K1 Computational Biology
K1 Biological Sciences not elsewhere classified
K1 Chemical Sciences not elsewhere classified
K1 Physical Sciences not elsewhere classified
K1 Information Systems not elsewhere classified
K1 catalyzed asymmetric addition
K1 1 ′</ b
K1 chiral diene (<
K1 dynamic kinetic resolution
K1 3 </ b
K1 2 </ b
K1 1 </ b
K1 5 ‑ carbonyl
K1 kinetic resolution
K1 chiral catalyst
K1 trans </
K1 organoboronic acid
K1 high diastereo
K1 fast racemization
K1 dienolate followed
K1 achiral isomer
K1 >- cycloalkanone
K1 >)- fc
K1 (−)- cannabidiol
JF doi:10.1021/acs.orglett.3c04281.s001
LK http://dx.doi.org/https://doi.org/10.1021/acs.orglett.3c04281.s001
DO https://doi.org/10.1021/acs.orglett.3c04281.s001
SF ELIB - SuUB Bremen

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