Academic Journal

Ringing the Changes: Effects of Heterocyclic Ring Size on Stereoselectivity in [(η 5 -C 5 Me 5)RhCl], [(η 5 -C 5 Me 5)IrCl] and [Ru(η 6 -cymene)Cl] Complexes of Chiral 3-Amino-1-Azacycles.

التفاصيل البيبلوغرافية
العنوان: Ringing the Changes: Effects of Heterocyclic Ring Size on Stereoselectivity in [(η 5 -C 5 Me 5)RhCl], [(η 5 -C 5 Me 5)IrCl] and [Ru(η 6 -cymene)Cl] Complexes of Chiral 3-Amino-1-Azacycles.
المؤلفون: Vladimirov, Vladimir Y.1 (AUTHOR) vladimirovvy@cardiff.ac.uk, Charrier-Chardin, Matheo1 (AUTHOR), Kariuki, Benson M.1 (AUTHOR), Ward, Benjamin D.1 (AUTHOR), Newman, Paul D.1 (AUTHOR) newmanp1@cardiff.ac.uk
المصدر: Molecules. Oct2024, Vol. 29 Issue 19, p4659. 12p.
مصطلحات موضوعية: *DIAMINES, *STEREOSELECTIVE reactions, *KETONES, *TRANSFER hydrogenation
مستخلص: Ring size-dependent diastereoselective coordination of unsymmetrical diamines containing one azacyclic nitrogen and one exocyclic nitrogen to [(η5-C5Me5)MCl]+ cores where M = Rh, Ir and [Ru(η6-cymene)Cl]+ is reported herein. Total stereoselectivity was observed with the six- and seven-membered azacycles, whereas the five-derivative proved poorly selective. All complexes were active for transfer hydrogenation but showed no enantioselectivity with prochiral ketones. [ABSTRACT FROM AUTHOR]
قاعدة البيانات: Academic Search Index
الوصف
تدمد:14203049
DOI:10.3390/molecules29194659