Synthesis and reactivity of phenyliodonium ylides of benz [b] oxepine-3, 5 (2H, 4H)-diones
S Spyroudis, P Tarantili
Index: Spyroudis, Spyros; Tarantili, Petroula Journal of Organic Chemistry, 1993 , vol. 58, # 18 p. 4885 - 4889
Full Text: HTML
Citation Number: 31
Abstract
Zwitterionic iodonium compounds (ZIC), a major class of polyvalent iodine compounds, are attractive and versatile reagents in organic synthesis. Koser has reviewed the early chemistry of this class, l and Varvoglis2 has thoroughly reviewed the chemistry of ZIC up to 1991. ZIC react with both electrophiles and nucleophiles, give rise to carbenes, afford transylidation and rearrangement products, and have oxidative properties. One of the ...
Related Articles:
[Zhang, Zuhui; Pan, Chongfeng; Wang, Zhiyong Chemical Communications, 2007 , # 44 p. 4686 - 4688]
[Jean, Mickael; Van De Weghe, Pierre Tetrahedron Letters, 2011 , vol. 52, # 27 p. 3509 - 3513]
Conjugate addition of cuprate reagents to chromones: A route to 2-substituted chroman-4-ones
[Saengchantara, Suthiweth T.; Wallace, Timothy W. Tetrahedron, 1990 , vol. 46, # 8 p. 3029 - 3036]
Hydantoin bioisosteres. In vivo active spiro hydroxy acetic acid aldose reductase inhibitors
[Lipinski, Christopher A.; Aldinger, Charles E.; Beyer, Thomas A.; Bordner, Jon; Burdi, Douglas F.; et al. Journal of Medicinal Chemistry, 1992 , vol. 35, # 12 p. 2169 - 2177]
Conjugate addition of cuprate reagents to chromones: A route to 2-substituted chroman-4-ones
[Saengchantara, Suthiweth T.; Wallace, Timothy W. Tetrahedron, 1990 , vol. 46, # 8 p. 3029 - 3036]