Tetrahedron Letters

PPh 3/halogenating agent-mediated highly efficient ring opening of activated and non-activated aziridines

M Kumar, SK Pandey, S Gandhi, VK Singh

Index: Kumar, Manoj; Pandey, Sanjay K.; Gandhi, Shikha; Singh, Vinod K. Tetrahedron Letters, 2009 , vol. 50, # 3 p. 363 - 365

Full Text: HTML

Citation Number: 15

Abstract

We report here the use of PPh3/halogenating agents as highly efficient reagents for the ring opening of aziridines with halides. The method works effectively for both activated and non- activated aziridines, and furnishes the products in excellent yields within a short period of time.

Related Articles:

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]

Lewis base catalyzed ring opening of aziridines with silylated nucleophiles

[Minakata, Satoshi; Okada, Yuriko; Oderaotoshi, Yoji; Komatsu, Mitsuo Organic Letters, 2005 , vol. 7, # 16 p. 3509 - 3512]

Lewis base catalyzed ring opening of aziridines with silylated nucleophiles

[Minakata, Satoshi; Okada, Yuriko; Oderaotoshi, Yoji; Komatsu, Mitsuo Organic Letters, 2005 , vol. 7, # 16 p. 3509 - 3512]

More Articles...