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Chirality Transfer of Stereogenic Boron Centers Enabled by ..:
Yannick Stöckl
;
Katrin Gugeler
;
Celine M. Holzwarth
...
doi:10.1021/acs.organomet.3c00472.s002. , 2024
Link:
https://doi.org/10.1021/acs.organomet.3c00472.s002
RT Journal T1
Chirality Transfer of Stereogenic Boron Centers Enabled by a S N 2‑Type Mechanism
UL https://suche.suub.uni-bremen.de/peid=base-ftdeakinunifig:oai:figshare.com:article_25003383&Exemplar=1&LAN=DE A1 Yannick Stöckl A1 Katrin Gugeler A1 Celine M. Holzwarth A1 Wolfgang Frey A1 Sascha Wegner A1 Birgit Claasen A1 Anna Zens A1 Dietrich Gudat A1 Christian P. Sindlinger A1 Johannes Kästner A1 Sabine Laschat YR 2024 K1 Biochemistry K1 Microbiology K1 Genetics K1 Evolutionary Biology K1 Chemical Sciences not elsewhere classified K1 Information Systems not elsewhere classified K1 unexpected steric effects K1 reaction intermediate could K1 likely reaction path K1 characterized using heteronuclear K1 challenging synthesis makes K1 additional experiments indicated K1 borate formation governs K1 successful chirality transfer K1 >- chelate effect K1 n </ sub K1 chirality transfer K1 borate anion K1 type breaking K1 stereocontrol prompted K1 quite robust K1 organometallic nucleophile K1 nmr spectroscopy K1 n </ K1 methodology proved K1 luminescent properties K1 inverse enantioselectivity K1 holistic understanding K1 earlier work K1 dft calculations K1 deeper investigation K1 compounds scarce K1 assisted pathway K1 >- chelates JF doi:10.1021/acs.organomet.3c00472.s002 LK http://dx.doi.org/https://doi.org/10.1021/acs.organomet.3c00472.s002 DO https://doi.org/10.1021/acs.organomet.3c00472.s002 SF ELIB - SuUB Bremen
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