Cycloaddition of homochiral imidazolinium ylides: A route to optically active pyrroloimidazoles
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference9 articles.
1. Annulation of imidazolines: A 1,3-dipolar cycloaddition route to pyrroloimidazoles, pyrrolidines and pyrroles
2. Enantiocontrolled construction of bicyclic proline derivatives via one-pot generation and intramolecular trapping of chiral stabilised azomethine ylids
3. Asymmetric [1,3]-dipolar cycloaddition reactions: synthesis of highly substituted proline derivatives
4. Asymmetric synthesis XVII : Facile generation of a chiral azomethine ylide via the CN(R,S) method
5. Jones, R.C.F.; Howard, K.J.; Snaith, J.S. following Letter.
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4. Asymmetric [3 + 2] Cycloaddition of Chiral N-Phosphonyl Imines with Methyl Isocyanoacetate for Accessing 2-Imidazolines with Switchable Stereoselectivity;The Journal of Organic Chemistry;2017-03-08
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