Identification | Back Directory | [Name]
(-)-N,N'-(1R,2R)-1,2-DIAMINOCYCLOHEXANEDIYLBIS(2-PYRIDINECARBOXAMIDE) | [CAS]
218290-24-5 | [Synonyms]
(R,R)-DACH-pyridyl Trost ligand (R,R)-DACH-pyridyl Trost ligand 95% Diaminocyclohexanediylbispyridinecarboxamide 2,6-Bis[(4R)-benzyl-2-oxazolin-2-yl]-pyridine trans-1,2-Bis(2-pyridinecarboxamido)cyclohexane (1R,2R)-1,2-Bis(2-pyridinecarboxamido)cyclohexane 1R,2R- N,N’-1,2-Diaminocyclohexanediylbis
(2-pyridinecarboxamide) (-)-N,N'-(1R,2R)-1,2-DIAMINOCYCLOHEXANEDIYLBIS(2-PYRIDINECARBOXAMIDE) (-)-N,N'-(1R,2R)-1,2-Diaminocyclohexanediylbis(2-pyridinecarboxamide),98% (1R,2R)-N,N'-1,2-Diaminocyclohexanediylbis(2-pyridinec
arboxamide),99%e.e. (-)-N,N'-(1R,2R)-1,2-Diaminocyclohexanediylbis(2-pyridinecarboxamide),min.98% (-)-N,N''-(1R,2R)-1,2-DIAMINOCYCLOHEXANEDIYLBIS(2-PYRIDINECARBOXAMIDE), MIN. 98% (-)-N,N'-(1R,2R)-1,2-Diaminocyclohexanediylbis(2-pyridinecarboxamide), min. 98% (R,R)-DACH-Pyridyl Trost Ligand | [Molecular Formula]
C18H20N4O2 | [MDL Number]
MFCD02684543 | [MOL File]
218290-24-5.mol | [Molecular Weight]
324.38 |
Questions And Answer | Back Directory | [Reaction]
- Ligands for Mo catalyzed asymmetric allylic substitutions. Especially useful for the synthesis of tertiary and quaternary stereocenters. Exclusive license for this technology acquired by ChiroTech and is protected by pending Stanford University patents.
- Dynamic kinetic asymmetric formation of tertiary and quaternary stereogenic centers.
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Energy Chemical
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Sigma-Aldrich
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