Stereospecific synthesis of acyclic unsaturated amino alcohols. A new approach to threo and erythro sphingosine

1983 ◽  
Vol 105 (13) ◽  
pp. 4499-4501 ◽  
Author(s):  
Ravi S. Garigipati ◽  
Steven M. Weinreb
1990 ◽  
Vol 31 (24) ◽  
pp. 3481-3484 ◽  
Author(s):  
Gianfranco Cainelli ◽  
Elisabetta Mezzina ◽  
Mauro Panunzio
Keyword(s):  

1996 ◽  
Vol 61 (2) ◽  
pp. 288-297 ◽  
Author(s):  
Vladimír Pouzar ◽  
Ivan Černý

New approach to the preparation of steroids with connecting bridge, based on an O-carboxymethyloxime (CMO) structure, and with terminal hydroxy group, is presented. 17-CMO derivatives of 3β-acetoxy- and 3β-methoxymethoxyandrost-5-en-17-one were condensed with α,ω-amino alcohols to give derivatives with a chain of seven to nine atoms. After THP-protection, these compounds were converted to 3-keto-4-ene derivatives. An alternative synthesis consisted in transformation of 17-CMO derivatives with bonded amino acids by reduction of the terminal carboxyl. The resulting compounds were designed as building blocks for the preparation of bis-haptens for sandwich immunoassays.


ARKIVOC ◽  
2012 ◽  
Vol 2012 (3) ◽  
pp. 181-192 ◽  
Author(s):  
Grzegorz Mlostoń ◽  
Adam M. Pieczonka ◽  
Korany A. Ali ◽  
Anthony Linden ◽  
Heinz Heimgartner
Keyword(s):  

Author(s):  
Ton That Thang ◽  
Maria de los A. Laborde ◽  
Alain Olesker ◽  
Gabor Lukacs

ChemInform ◽  
1989 ◽  
Vol 20 (27) ◽  
Author(s):  
T. T. THANG ◽  
M. A. LABORDE ◽  
A. OLESKER ◽  
G. LUKACS

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