Lewis base catalyzed ring opening of aziridines with silylated nucleophiles
S Minakata, Y Okada, Y Oderaotoshi, M Komatsu
Index: Minakata, Satoshi; Okada, Yuriko; Oderaotoshi, Yoji; Komatsu, Mitsuo Organic Letters, 2005 , vol. 7, # 16 p. 3509 - 3512
Full Text: HTML
Citation Number: 72
Abstract
Aziridines are very useful synthetic intermediates for the synthesis of functional materials and biologically active compounds. 1 For this reason, in previous studies, we developed some facile synthetic methods for producing aziridines through the introduction of an N1 unit to alkenes. 2 The reactivity of aziridines toward ring opening and expansion is dependent upon their extremely strained ring structures. Among the procedures of ring opening of aziridines, a ...
Related Articles:
[Kumar, Manoj; Pandey, Sanjay K.; Gandhi, Shikha; Singh, Vinod K. Tetrahedron Letters, 2009 , vol. 50, # 3 p. 363 - 365]
Polystyrene-supported TBD catalyzed ring-opening of N-tosylaziridines with silylated nucleophiles
[Matsukawa, Satoru; Harada, Takeru; Yasuda, Shiori Organic and Biomolecular Chemistry, 2012 , vol. 10, # 25 p. 4886 - 4890]