ChemInform Abstract: Chemistry of the 1,3,5-Triaza-2-phosphorin-4,6-diones. Part 11. Base- Catalyzed Addition Reactions of 2-Oxo-2-hydro-1,3,5-trimethyl-1,3,5- triaza-2λ4-phosphorine-4,6-dione to the C=N Double Bond of 3- Thiazoline Heterocycles.

ChemInform ◽  
2010 ◽  
Vol 28 (11) ◽  
pp. no-no
Author(s):  
I. NEDA ◽  
T. KAUKORAT ◽  
P. G. JONES ◽  
R. SCHMUTZLER ◽  
H. GROEGER ◽  
...  
2019 ◽  
Vol 48 (48) ◽  
pp. 17729-17734 ◽  
Author(s):  
Juliane Schoening ◽  
Lukas John ◽  
Christoph Wölper ◽  
Stephan Schulz

Oxidative addition reactions of gallanediyl LGa and AsX3 yield gallaarsenes LGaAsGa(Cl)L (X = Cl 1; Br 2) with a Ga–As double bond.


2016 ◽  
Vol 45 (3) ◽  
pp. 577-583 ◽  
Author(s):  
Reinhard W. Hoffmann

This review covers free radical additions, which are initiated by the formal addition of a hydrogen atom to a CC double bond.


2011 ◽  
Vol 2011 (11) ◽  
pp. 1824-1832 ◽  
Author(s):  
Roberto Mosteiro ◽  
Alberto Fernández ◽  
Digna Vázquez-García ◽  
Margarita López-Torres ◽  
Antonio Rodríguez-Castro ◽  
...  

RSC Advances ◽  
2016 ◽  
Vol 6 (112) ◽  
pp. 111144-111147
Author(s):  
Wei Li ◽  
Wenlei Chu ◽  
Wen Jin ◽  
Xijiang Han ◽  
Yufei Ma ◽  
...  

PhS nitration products absorbed on Ag/Au NPs underwent nitro- and amino-group redox cycle reactions monitored using SERS spectra. I2 addition to the CC double bond was also confirmed with SERS.


1991 ◽  
Vol 56 (4) ◽  
pp. 886-904 ◽  
Author(s):  
Alois Vystrčil ◽  
Václav Křeček ◽  
Jiří Protiva ◽  
Miloš Buděšínský

The structure of anhydrobetulin II and its derivatives I, III and IV has been solved using 1H and 13C NMR spectra, mass spectra and chemical transformations. It has been proven that in addition reactions the trisubstituted double bond is attacked selectively from the α-side under formation of D/E cis-annelated derivatives VIII, X and XI. The 22-oxo derivative XIII exhibits an anomalous Cotton effect and, in contrast to its saturated analogue XXVII,it is not epimerized in alkaline medium. Trinordiketone XXI easily epimerizes to a mixture in which the 17βH-epimer XXIb predominates, trinorketone XXIV is stable only if the annelation of rings D and E is trans. These differences are explained in terms of steric interactions of substituents in position 19. The steric course of reduction of ketones XIII and XXIV with sodium borohydride is described.


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