The synthesis of unsymmetrically N-substituted chiral 1,4,7-triazacyclononanes.
about
Designed folding of pseudopeptides: the transformation of a configurationally driven preorganization into a stereoselective multicomponent macrocyclization reaction.Incorporation of Cobalt-Cyclen Complexes into Templated Nanogels Results in Enhanced Activity.Recent advances in catalytic asymmetric epoxidation using the environmentally benign oxidant hydrogen peroxide and its derivatives.The application of manganese complexes of ligands derived from 1,4,7-triazacyclononane in oxidative catalysis.Investigation of macrocyclisation routes to 1,4,7-triazacyclononanes: efficient syntheses from 1,2-ditosylamides.Inter- and intramolecular Mitsunobu reaction and metal complexation study: synthesis of S-amino acids derived chiral 1,2,3,4-tetrahydroquinoxaline, benzo-annulated [9]-N3 peraza, [12]-N4 peraza-macrocycles.
P2860
The synthesis of unsymmetrically N-substituted chiral 1,4,7-triazacyclononanes.
description
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name
The synthesis of unsymmetrically N-substituted chiral 1,4,7-triazacyclononanes.
@en
The synthesis of unsymmetrically N-substituted chiral 1,4,7-triazacyclononanes.
@nl
type
label
The synthesis of unsymmetrically N-substituted chiral 1,4,7-triazacyclononanes.
@en
The synthesis of unsymmetrically N-substituted chiral 1,4,7-triazacyclononanes.
@nl
prefLabel
The synthesis of unsymmetrically N-substituted chiral 1,4,7-triazacyclononanes.
@en
The synthesis of unsymmetrically N-substituted chiral 1,4,7-triazacyclononanes.
@nl
P2093
P2860
P356
P1476
The synthesis of unsymmetrically N-substituted chiral 1,4,7-triazacyclononanes.
@en
P2093
David M Benoit
J Erik W Scheuermann
Kevin F Sibbons
Majid Motevalli
Michael Watkinson
P2860
P304
P356
10.1039/B409259G
P577
2004-08-24T00:00:00Z