Synthesis of optically active lipopeptide analogs from the outer membrane of Escherichia coli.

栗村宗明， 竹元万寿美， 阿知波一雄

Index: Kurimura; Takemoto; Achiwa Chemical and Pharmaceutical Bulletin, 1991 , vol. 39, # 10 p. 2590 - 2596

Full Text: HTML

Citation Number: 14

Abstract

... Bull. 39(10) 2590—2596 (1991) Vol. 39, No. 10 Synthesis of Optically Active Lipopeptide Analogs from the Outer Membrane of Escherichia coli Muneaki KURIMURA, Masurni TAKEMOTO, and Kazuo ... Thus compound 11 was prepared according to Achiwa's method. ...

Related Articles:

Mild, versatile, and chemoselective indium (III) triflate-catalyzed deprotection of acetonides under microwave heating conditions

[Golden, Kathryn C.; Gregg, Brian T.; Quinn, John F. Tetrahedron Letters, 2010 , vol. 51, # 31 p. 4010 - 4013]

Synthesis and. beta.-adrenergic antagonist activity of stereoisomeric practolol and propranolol derivatives

[Leftheris, Katerina; Goodman, Murray Journal of Medicinal Chemistry, 1990 , vol. 33, # 1 p. 216 - 223]

Absolute configuration of glycerol derivatives. 3. Synthesis and Cupra A circular dichroism spectra of some chiral 3-aryloxy-1, 2-propanediols and 3-aryloxy-1-amino-2 …

[Nelson,W.L. et al. Journal of Organic Chemistry, 1977 , vol. 42, p. 1006 - 1012]

Synthesis and activity of optical isomers of nipradilol.

[Shiratsuchi; Kawamura; Akashi; Ishihama; Nakamura; Takenaka Chemical and Pharmaceutical Bulletin, 1987 , vol. 35, # 9 p. 3691 - 3698]

Asymmetric enzymatic hydrolysis of prochiral 2-O-allylglycerol ester derivatives

[Wirz, Beat; Schmid, Rudolf; Foricher, Joseph Tetrahedron: Asymmetry, 1992 , vol. 3, # 1 p. 137 - 142]

More Articles...