83815-92-3Relevant articles and documents
Macrocycles containing tin. Syntheses of symmetrical macrocycles containing two or four diphenylstanna units
Azuma, Yutaka,Newcomb, Martin
, p. 9 - 14 (2008/10/08)
The syntheses of macrocycles containing two diphenylstanna moieties, c-[Ph2Sn(CH2)n-]2 (1, n = 4, 5, 6, 8, 10, 12), and four diphenylstanna moieties, c-[Ph2Sn(CH2)n-]4 (2, same n), are reported. α,ω-Bis-(bromomagnesio)alkanes reacted with Ph3SnCl to give α,ω-bis(triphenylstannyl)alkanes which upon treatment with HBr gave α,ω-bis(bromodiphenylstannyl)alkanes 4. Compounds 4 reacted with the corresponding chain length α,ω-bis(bromomagnesio)alkanes to give 1 and 2. Alternatively, good yields of 1 (n = 4, 5, 6, 8) were obtained by converting 4 to dilithium reagents 7 which were allowed to react with α,ω-dibromoalkanes. Good yields of 2 (n = 4-6) were obtained by first treating 4 with Cl(CH2)nMgBr to give dichlorides which were then allowed to react with 7 in a second step. Purifications of the macrocycles and several synthetic intermediates were effected by preparative reverse-phase chromatography. The macrocyclic products were characterized by NMR spectroscopy, molecular weight determinations, and elemental analyses.
Macrocycles containing tin. Two syntheses of 1, 1, 6, 6, 11, 11, 16, 16-octaphenyl-1, 6, 11, 16-tetrastannacycloeicosane and a synthesis of 1, 1, 6, 6-tetraphenyl-1, 6-distannacyclodecane
Newcomb, Martin,Azuma, Yutaka,Courtney, Arlene R.
, p. 175 - 177 (2008/10/08)
The title syntheses are described. The synthetic and purification and analytical methods employed are of general utility for the preparation and functionalization of members of this class of compounds.
