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1 Ergebnisse
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Synthesis of Dihydropyridine Spirocycles by Semi-Pinacol-Dr..:
Joseph C. Abell (14375304)
;
Christian P. Bold (4677862)
;
Laia Vicens (6476111)
...
https://figshare.com/articles/journal_contribution/Synthesis_of_Dihydropyridine_Spirocycles_by_Semi-Pinacol-Driven_Dearomatization_of_Pyridines/21861420. , 2023
Link:
https://doi.org/10.1021/acs.orglett.2c04095.s001
RT Journal T1
Synthesis of Dihydropyridine Spirocycles by Semi-Pinacol-Driven Dearomatization of Pyridines
UL https://suche.suub.uni-bremen.de/peid=base-ftunivfreestate:oai:figshare.com:article_21861420&Exemplar=1&LAN=DE A1 Joseph C. Abell (14375304) A1 Christian P. Bold (4677862) A1 Laia Vicens (6476111) A1 Tom Jentsch (14375307) A1 Noelia Velasco (5183720) A1 Jasper L. Tyler (14375313) A1 Robert N. Straker (14375316) A1 Adam Noble (1331373) A1 Varinder K. Aggarwal (1363332) YR 2023 K1 Biophysics K1 Biochemistry K1 Cell Biology K1 Molecular Biology K1 Physiology K1 Pharmacology K1 Biotechnology K1 Sociology K1 Immunology K1 Chemical Sciences not elsewhere classified K1 spirocyclic dihydropyridines via K1 beneficial pharmacokinetic properties K1 operationally simple synthesis K1 induced dearomative semi K1 various points K1 synthetic utility K1 spirocyclization precursors K1 routine incorporation K1 ketone functionalities K1 highly rigid K1 driven dearomatization K1 dimensional structures JF https://figshare.com/articles/journal_contribution/Synthesis_of_Dihydropyridine_Spirocycles_by_Semi-Pinacol-Driven_Dearomatization_of_Pyridines/21861420 LK http://dx.doi.org/https://doi.org/10.1021/acs.orglett.2c04095.s001 DO https://doi.org/10.1021/acs.orglett.2c04095.s001 SF ELIB - SuUB Bremen
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