mixed anhydride method

Keyword(s):  
2002 ◽  
Vol 67 (11) ◽  
pp. 1709-1718 ◽  
Author(s):  
Miroslav Reschel ◽  
Miloš Buděšínský ◽  
Ivan Černý ◽  
Vladimír Pouzar ◽  
Pavel Drašar

Linear oligoesters based on etienic acid (3β-hydroxyandrost-5-ene-17β-carboxylic acid) containing 2-4 steroid units were prepared employing mixed anhydride esterification. NMR spectra of the oligomeric steroids have been fully assigned.


2009 ◽  
Vol 112 (1) ◽  
pp. 44-51 ◽  
Author(s):  
F. Lyon ◽  
M.-F. Thevenon ◽  
A. Pizzi ◽  
G. Tondi ◽  
A. Despres ◽  
...  

ChemInform ◽  
2012 ◽  
Vol 43 (48) ◽  
pp. no-no
Author(s):  
James McNulty ◽  
Ramesh Vemula ◽  
Venkatesan Krishnamoorthy ◽  
Al Robertson

2003 ◽  
Vol 81 (12) ◽  
pp. 1438-1442 ◽  
Author(s):  
Wojciech Czardybon ◽  
Arkadiusz Klys ◽  
John Warkentin ◽  
Nick Henry Werstiuk

2-Acetoxy-2-methoxy-5,5-dimethyl-Δ3-1,3,4-oxadiazoline undergoes two competitive 1,3-dipolar cycloreversions at 110 °C. It loses N2, presumably to afford a short-lived carbonyl ylide that fragments to acetone and acetoxy(methoxy)carbene. It also forms 2-diazopropane and the appropriate mixed anhydride. It is the only currently known source of acetoxy(methoxy)carbene. Key words: acetoxy(methoxy)carbene, 2-diazopropane, 1,3-dipolar cycloreversion.


1983 ◽  
Vol 6 (3) ◽  
pp. 326
Author(s):  
W.M.M. Schaaper ◽  
H.C. Beyerman
Keyword(s):  

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