Memory of Chirality in 1,4-Benzodiazepin-2-ones
Memory of chirality (MOC) is an emerging strategy in asymmetric synthesis. It has been applied to enolate chemistry, reactions involving carbocation intermediates, and to radical systems. In this strategy the chirality of an enantiopure reactant is transferred to the dynamic chirality of a reactiv...
Main Author: | DeGuzman, Joseph Christopher |
---|---|
Other Authors: | Chemistry |
Format: | Others |
Published: |
Virginia Tech
2014
|
Subjects: | |
Online Access: | http://hdl.handle.net/10919/28079 http://scholar.lib.vt.edu/theses/available/etd-06192006-161356/ |
Similar Items
-
Low Temperature Dynamic Chromatography for the Separation of the Interconverting Conformational Enantiomers of the Benzodiazepines Clonazolam, Flubromazolam, Diclazepam and Flurazepam
by: Roberta Franzini, et al.
Published: (2021-06-01) -
Enantiomeric Recognition and Separation by Chiral Nanoparticles
by: Ankur Gogoi, et al.
Published: (2019-03-01) -
Racemic and Meso Crystal Structures of an Axial-Chiral Spirobi-(dinaphthoazepin)ium Salt: Emergence of an S<sub>4</sub>-Symmetric Molecule
by: Philipp Honegger, et al.
Published: (2021-07-01) -
Deracemization of Axially Chiral Nicotinamides by Dynamic Salt Formation with Enantiopure Dibenzoyltartaric Acid (DBTA)
by: Fumitoshi Yagishita, et al.
Published: (2013-11-01) -
Nanoparticle-based Chemiluminescence for Chiral Discrimination of Thiol-Containing Amino Acids
by: Maryam Shahrajabian, et al.
Published: (2018-09-01)