Issue 6, 1997
From the journal:

Mendeleev Communications

Methyl 2-trifluoromethylaziridine-2-carboxylate: stereodirected N-halogenation from the sterically more hindered side

Vladimir V. Rozhkov,   Kirill N. Makarov,   Sergey N. Osipov,   Ivan I. Chervin,   Anatolii V. Ignatenko  and  Remir G. Kostyanovsky  

Abstract

N-Fluorination and N-chlorination of methyl 2-trifluoromethylaziridine-2-carboxylate occurs predominantly from the more hindered side owing to the fixed orientation of the lone electron pair of the N atom caused by the formation of an intramolecular H-bond.

About
Cited by
Related
Download options Please wait...

Article information

DOI
https://doi.org/10.1070/MC1997v007n06ABEH000831
Article type
Paper

Mendeleev Commun., 1997,7, 229-230

Permissions

Request permissions

Methyl 2-trifluoromethylaziridine-2-carboxylate: stereodirected N-halogenation from the sterically more hindered side

V. V. Rozhkov, K. N. Makarov, S. N. Osipov, I. I. Chervin, A. V. Ignatenko and R. G. Kostyanovsky, Mendeleev Commun., 1997, 7, 229 DOI: 10.1070/MC1997v007n06ABEH000831

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements