Issue 2, 1997
From the journal:

Chemical Communications

N-Methylidene[bis(trimethylsilyl)methyl]amine: the first isolable and stable monomeric methanimine allowing thermal [2 + 2] cycloadditions with ketenes

Claudio Palomo,   Jesus M. Aizpurua,   Marta Legido  and  Regina Galarza  

Abstract

N-Methylidene[bis(trimethylsilyl)methyl]amine acts as a stable methanimine synthon [CH 2 [double bond, length as m-dash]NH] equivalent in [2 + 2] cycloadditions to ketenes, generated from acid chlorides and triethylamine, to provide 4-unsubstituted β-lactams in a single step.

About
Cited by
Related
Download options Please wait...

Article information

DOI
https://doi.org/10.1039/A607348D
Article type
Paper

Chem. Commun., 1997, 233-234

Permissions

Request permissions

N-Methylidene[bis(trimethylsilyl)methyl]amine: the first isolable and stable monomeric methanimine allowing thermal [2 + 2] cycloadditions with ketenes

C. Palomo, J. M. Aizpurua, M. Legido and R. Galarza, Chem. Commun., 1997, 233 DOI: 10.1039/A607348D

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.

Social activity

Spotlight

Advertisements