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A General Procedure for the Synthesis of Unsymmetrically Substituted Tris(β-oximinoalkyl)amines Full article

Journal Synthesis-Stuttgart
ISSN: 1437-210X , E-ISSN: 0039-7881
Output data Year: 2011, Volume: 2011, Number: 09, Pages: 1403-1412 Pages count : 10 DOI: 10.1055/s-0030-1259995
Authors Sukhorukov Alexey 1 , Ioffe Sema 1 , Semakin Artem 1 , Tartakovsky Vladimir 1
Affiliations
1 N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences,

Abstract: A first general approach to the synthesis of unsymmetrically substituted tris(β-oximinoalkyl)amines containing two or three different β-oximinoalkyl fragments has been developed. This procedure employs available aliphatic nitro compounds as starting building blocks and their silylation as the key step. This approach provides an efficient strategy for the diversity-oriented synthesis of 1,4,6,10-tetraazaadamantane derivatives.
Cite: Sukhorukov A. , Ioffe S. , Semakin A. , Tartakovsky V.
A General Procedure for the Synthesis of Unsymmetrically Substituted Tris(β-oximinoalkyl)amines
Synthesis-Stuttgart. 2011. V.2011. N09. P.1403-1412. DOI: 10.1055/s-0030-1259995 WOS Scopus OpenAlex
Identifiers:
Web of science: WOS:000289713800011
Scopus: 2-s2.0-79954996167
OpenAlex: W2007055815
Citing:
DB Citing
OpenAlex 3
Scopus 11
Web of science 11
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