Synthesis of pyrrolidine ring-fused metallofullerene derivatives

47Citations
Citations of this article
7Readers
Mendeley users who have this article in their library.
Get full text

Abstract

The azomethine ylide generated from the reaction of sarconsine and formaldehyde adds to Gd@C82 to give the mono- through octo-adducts, while the direct interaction of sarcosine with Gd@C82 yields only the mono-adduct, which is characterized by HPLC, MALDI-TOF MS, UV-Vis-NIR and FT-IR. The reaction mechanism for this reaction is proposed to be a 1,3-dipolar addition. © 2004 Elsevier Ltd. All rights reserved.

Cite

CITATION STYLE

APA

Lu, X., He, X., Feng, L., Shi, Z., & Gu, Z. (2004). Synthesis of pyrrolidine ring-fused metallofullerene derivatives. Tetrahedron, 60(16), 3713–3716. https://doi.org/10.1016/j.tet.2004.02.061

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free