A micromethod for the determination of the absolute stereochemistry at C-15 of prostanoids and related compounds
G Just, H Oh
Index: Just, George; Oh, Hunseung Tetrahedron Letters, 1980 , vol. 21, p. 3667 - 3668
Full Text: HTML
Citation Number: 11
Abstract
Abstract Reductive ozonolysis of Δ 13-15-acetoxy prostanoids, followed by reaction of the resulting 2-acetoxyheptanal with l-ephedrine, gives oxazolidines whose R, values on tlc are characteristic of the chirality of the acetoxy group, thus permitting the determination of the
Related Articles:
Ozonolysis of acetic acid 1-vinyl-hexyl ester in a falling film microreactor
[Steinfeldt, Norbert; Abdallah, Radwan; Dingerdissen, Uwe; Jaehnisch, Klaus Organic Process Research and Development, 2007 , vol. 11, # 6 p. 1025 - 1031]
Synthesis and properties of natural occurring α-hydroxyaldehydes
[Kern, Werner; Spiteller, Gerhard Tetrahedron, 1996 , vol. 52, # 12 p. 4347 - 4362]
Synthesis and properties of natural occurring α-hydroxyaldehydes
[Kern, Werner; Spiteller, Gerhard Tetrahedron, 1996 , vol. 52, # 12 p. 4347 - 4362]
Synthesis and properties of natural occurring α-hydroxyaldehydes
[Kern, Werner; Spiteller, Gerhard Tetrahedron, 1996 , vol. 52, # 12 p. 4347 - 4362]
Ozonolysis of acetic acid 1-vinyl-hexyl ester in a falling film microreactor
[Steinfeldt, Norbert; Abdallah, Radwan; Dingerdissen, Uwe; Jaehnisch, Klaus Organic Process Research and Development, 2007 , vol. 11, # 6 p. 1025 - 1031]