1,2-Methyl shift between platinum and the coordinated aryl group in the reaction of methyl iodide with 2,6-bis[(dimethylamino)methyl]phenyl-N,N',C complexes of platinum(II). X-ray crystal structure of the arenonium-platinum compound [Pt(o-tolyl)(MeC6H3(CH2NMe2)2-o,o')]I

1985 ◽  
Vol 107 (10) ◽  
pp. 2891-2898 ◽  
Author(s):  
Jos Terheijden ◽  
Gerard Van Koten ◽  
Ico C. Vinke ◽  
Anthony L. Spek
2002 ◽  
Vol 57 (4) ◽  
pp. 444-452 ◽  
Author(s):  
Maged K.G Mekhael ◽  
Richard J. Smith ◽  
Stefan Bienz ◽  
Anthony Linden ◽  
Heinz Heimgartner

2,2,N-Trimethyl-N-phenyl-2H-azirin-3-amine (1a) was prepared by successive treatment of 2,N-dimethyl-N-phenylpropanamide (18) with phosgene, triethylamine, and sodium azide. Reaction of 1a in THF solution with boron trifluoride gave 2-amino-1,3,3-trimethyl-3H-indolium tetrafluoroborate (19) in high yield.T he latter reacted with acetic anhydride in pyridine to give a mixture of N-(2,3-dihydro-1,3,3-trimethylindol-2-yliden)acetamide (22) and 2,3-dihydro- 1,3,3-trimethylindol-2-one (21).On hydrolysis with aqueous HCl, 22 was converted to 21.T he molecular structures of 19 and 22 were established by X-ray crystal structure determination.


2007 ◽  
Vol 72 (8) ◽  
pp. 985-995 ◽  
Author(s):  
Martin Lamač ◽  
Ivana Císařová ◽  
Petr Štěpnička

Treatment of racemic 1-(diphenylphosphanyl)-2-[(methoxycarbonyl)methyl]ferrocene successively with NaN(SiMe3)2 and methyl iodide affords the C-alkylated product, 1-(diphenylphosphanyl)-2-[1-(methoxycarbonyl)ethyl]ferrocene (6), as a mixture of diastereoisomers in ca. 10:1 ratio, from which the major (S,Rp/R,Sp)-diastereoisomer is easily isolated by crystallisation. (S,Rp/R,Sp)-6 reacts with [Pd(LNC)(MeCN)2]ClO4 (LNC = 2-[(dimethylamino-κN)- methyl]phenyl-κC1) to give the cationic bis-chelate complex (S,Rp/R,Sp)-[Pd(LNC)(6-κ2O,P)]- ClO4 (9). The structures of (S,Rp/R,Sp)-6 and 9 have been determined by single-crystal X-ray diffraction. Hydrolysis of ester 6 to the corresponding carboxylic acid proved to be difficult, being complicated by racemisation at the chiral carbon atom and oxidation of the phosphanyl group.


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