| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1326440 | Journal of Organometallic Chemistry | 2005 | 5 Pages |
Abstract
A high yield strategy for obtaining N-protected carboranyl amino acids from readily available 3-amino-o-carboranes was elaborated. Deprotection of N-acylated carborane amino acids is studied in acidic media. Depending on the procedure employed, closo- or nido-carborane amino acids were obtained.
Related Topics
Physical Sciences and Engineering
Chemistry
Inorganic Chemistry
Authors
Valentina A. Ol'shevskaya, Rami Ayuob, Zhanna G. Brechko, Pavel V. Petrovskii, Elena G. Kononova, Galina L. Levit, Victor P. Krasnov, Valery N. Charushin, Oleg N. Chupakhin, Valery N. Kalinin,