A catalytic asymmetric synthesis of chiral glycidic acid derivatives through chiral dioxirane-mediated catalytic asymmetric epoxidation of cinnamic acid derivatives
R Imashiro, M Seki
Index: Imashiro, Ritsuo; Seki, Masahiko Journal of Organic Chemistry, 2004 , vol. 69, # 12 p. 4216 - 4226
Full Text: HTML
Citation Number: 71
Abstract
A novel and practical asymmetric synthesis of chiral glycidic acid derivatives involving methyl (2 R, 3 S)-3-(4-methoxyphenyl) glycidate ((2 R, 3 S)-2a), a key intermediate for diltiazem hydrochloride (1), was developed. Treatment of methyl (E)-4-methoxycinnamate ((E)-3a) with chiral dioxirane, generated in situ from a catalytic amount (5 mol%) of an 11- membered C 2-symmetric binaphthyl ketone (R)-7a, provided (2 R, 3 S)-2a in 92% yield ...
Related Articles:
[Sharma, Dharminder; Kumar, Sandeep; Shil, Arun K.; Guha, Nitul Ranjan; Bandna; Das, Pralay Tetrahedron Letters, 2012 , vol. 53, # 52 p. 7044 - 7051]
[Appelberg, Ulf; Mohell, Nina; Hacksell, Uli Bioorganic and Medicinal Chemistry Letters, 1996 , vol. 6, # 4 p. 415 - 420]
[Peterson, John R.; Russell, Morley E.; Surjasasmita, Irawan B. Journal of Chemical & Engineering Data, 1988 , vol. 33, # 4 p. 534 - 537]
[Appelberg, Ulf; Mohell, Nina; Hacksell, Uli Bioorganic and Medicinal Chemistry Letters, 1996 , vol. 6, # 4 p. 415 - 420]
[Appelberg, Ulf; Mohell, Nina; Hacksell, Uli Bioorganic and Medicinal Chemistry Letters, 1996 , vol. 6, # 4 p. 415 - 420]