ChemInform Abstract: AZIDINIUM SALTS. 21. DIAZO GROUP TRANSFER TO AMINO ARENES AND AMINO HETARENES S USING AZIDINIUM SALTS- SYNTHESIS OF CONDENSED V-TRIAZOLES

1978 ◽  
Vol 9 (18) ◽  
Author(s):  
H. BALLI ◽  
L. FELDER
Keyword(s):  
1976 ◽  
Vol 31 (5) ◽  
pp. 586-588 ◽  
Author(s):  
Klaus-Peter Zeller

The synthesis of 5-diazo-5-[13C]-homoadamantan-4-one (12) is achieved by ring expansion of adamantanone with 13C-labelled diazomethane, conversion of the resulting 4-[13C]-homoadamantan-4-one (10) to the hydroxymethylene compound (11), followed by deformylative diazo group transfer reaction. The photolysis of 12 with pyrex filtered UV-light in dioxane-water (10:1) yields adamantan-2-carboxylic acid containing all the label in the 2-position of the adamantane skeleton. The total absence of isotope scrambling excludes the intermediate formation of the polycyclic oxiren (16) (Scheme 3).


1981 ◽  
Vol 36 (9) ◽  
pp. 1149-1152 ◽  
Author(s):  
Heinz Dürr ◽  
Gerhard Hauck ◽  
Wolfgang Brück ◽  
Helge Kober

AbstractPolymer anchored sulfonylazide is compared with its efficiency in the diazogroup transfer reaction of tosylazide. The resulting yields with the polymeric reaction are slightly lower than with tosylazide. However the greater thermostability of polymeric sulfonyl azide and its workup procedure make this alternative very attractive for synthesis. The reaction of polymeric sulfonyl azide with cyclic polyenes gives very small yields compared with the monomeric reaction. The attempt to generate diazocyclononatetraene by an alternative route leads only to the secondary product namely indene. At low temperature, and intermediate diazo-compound is, however, observed, which is tentatively assigned to structure 12.


2003 ◽  
pp. 134-134 ◽  
Author(s):  
Rick L. Danheiser ◽  
Raymond F. Miller ◽  
Ronald G. Brisbois
Keyword(s):  

2019 ◽  
Vol 25 (7) ◽  
pp. 1727-1732 ◽  
Author(s):  
Grant B. Frost ◽  
Michaela N. Mittelstaedt ◽  
Christopher J. Douglas

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