A novel isocyanide-based multicomponent reaction: An easy access to substituted propionamides and succinimides / Mironov M.A., Ivantsova M.N., Mokrushin V.S. // Synlett. - 2006. - V. , l. 4. - P. 615-617.

ISSN:

09365214

Type:

Article

Abstract:

A new approach to the design of multicomponent reactions is introduced. As a result the novel reaction of gem-diactivated olefins with 4-nitrophenol and isocyanides leading to substituted propionamides or succinimides was discovered. © Georg Thieme Verlag Stuttgart.

Author keywords:

Combinatorial chemistry; Isocyanides; Multicomponent reactions; Nucleophilic additives; Reaction design

Index keywords:

4 nitrophenol; alkene derivative; cyanide; propionamide derivative; succinimide derivative; article; chemical reaction; chemical structure; combinatorial chemistry; reaction analysis; synthesis

DOI:

10.1055/s-2006-933104

Смотреть в Scopus:

https://www.scopus.com/inward/record.uri?eid=2-s2.0-33645014816&doi=10.1055%2fs-2006-933104&partnerID=40&md5=6a4d3d8968a0658c03a7d04bbc826012

Соавторы в МНС:

Другие поля

Поле	Значение
Link	https://www.scopus.com/inward/record.uri?eid=2-s2.0-33645014816&doi=10.1055%2fs-2006-933104&partnerID=40&md5=6a4d3d8968a0658c03a7d04bbc826012
Affiliations	Department of Technology of Organic Synthesis, TOSLab, Urals State Technical University, 620002 Ekaterinburg, Russian Federation
Author Keywords	Combinatorial chemistry; Isocyanides; Multicomponent reactions; Nucleophilic additives; Reaction design
Chemicals/CAS	4 nitrophenol, 100-02-7; cyanide, 57-12-5
References	(2005) Multicomponent Reactions, , Zhu, J.; Bienayme, H., Eds.; WILEY-VCH Verlag: Weinheim; Burke, M.D., Schreiber, S.L., (2004) Angew. Chem. Int. Ed., 43, p. 46; Pauvannan, K., (1999) Tetrahedron Lett., 40, p. 1851; Lee, D., Sello, J.K., Schreiber, S.L., (2000) Org. Lett., 2, p. 709; Zhu, J., (2003) Eur. J. Org. Chem., p. 1133; Weber, L., Illgen, K., Almstetter, M., (1999) Synlett, p. 366; Doemling, A., (2000) Curr. Opin. Chem. Biol., 4, p. 318; Doemling, A., (2002) Curr. Opin. Chem. Biol., 6, p. 306; Mironov, M.A., Mokrushin, V.S., Maltsev, S.S., (2003) Synlett, p. 943; Ugi, I., Doemling, A., (2000) Angew. Chem. Int. Ed., 39, p. 3168; Saegusa, T., Ito, Y., Tomita, S., Kinoshita, H., Takaishi, N., (1971) Tetrahedron, 27, p. 27; Shaabani, A., Teimouri, M.B., Bijanzadeh, H.R., (2002) Tetrahedron Lett., 43, p. 9151; Nair, V., Menon, R.S., Vinod, A.U., Viji, S., (2002) Tetrahedron Lett., 43, p. 2293; Mironov, M.A., Ivantsova, M.N., Tokareva, M.I., Mokrushin, V.S., (2005) Tetrahedron Lett., 46, p. 3957; note; note; El Kaïm, L., Grimaud, L., Oble, J., (2005) Angew. Chem. Int. Ed., 44, p. 7961; Schmidt, R.R., (1965) Chem. Ber., 98, p. 346; note; note
Correspondence Address	Mironov, M.A.; Department of Technology of Organic Synthesis, TOSLab, Urals State Technical University, 620002 Ekaterinburg, Russian Federation; email: mirma@htf.ustu.ru
CODEN	SYNLE
Language of Original Document	English
Abbreviated Source Title	Synlett
Source	Scopus