Authors Mankaev, BN; Zaitsev, KV; Kuchuk, EA; Vershinina, MV; Zaitseva, GS; Egorov, MP; Karlov, SS in SPRINGER published article about RING-OPENING POLYMERIZATION; DIAMIDOAMINE LIGANDS; TRIMETHYLENE CARBONATE; TIN(II) INITIATORS; CYCLIC ESTERS; COMPLEXES; LACTIDE; CATALYSTS; 1-HEXENE; CONTAIN in [Mankaev, B. N.; Zaitsev, K., V; Kuchuk, E. A.; Vershinina, M. V.; Zaitseva, G. S.; Egorov, M. P.; Karlov, S. S.] Russian Acad Sci, ND Zelinsky Inst Organ Chem, 47 Leninsky Prosp, Moscow 119991, Russia; [Mankaev, B. N.; Zaitsev, K., V; Kuchuk, E. A.; Vershinina, M. V.; Zaitseva, G. S.; Karlov, S. S.] Moscow MV Lomonosov State Univ, Dept Chem, 1,Build 3, Moscow 119991, Russia in 2019.0, Cited 38.0. HPLC of Formula: C7H8O. The Name is Benzyl Alcohol. Through research, I have a further understanding and discovery of 100-51-6
The reactions of 3-benzyl-1,5-ditosyl-1,3,5-triazapentane (1) and 3-benzyl-1,5-dimesityl-1,3,5-triazapentane (2) with one equivalent of Lappert’s germylene or stannylene (M[N(SiMe3)(2)](2), where M = Ge, Sn) produced germylenes and stannylenes of the general formula PhCH2N(CH2CH2NR)(2)M, where M = Ge, R = 4-MeC6H4SO2- (3); 2,4,6-Me3C6H2- (5); M = Sn, R = 4-MeC6H4SO2- (4); 2,4,6-Me3C6H2- (6), in satisfactory yields. According to NMR data (H-1, C-13, Sn-119), stannylenes 4 and 6 are monomeric in solution, and the coordination number of tin is four. The synthesized stannylenes exhibited very high (compound 4) and moderate (compound 6) activity as initiators for bulk polymerization of epsilon-caprolactone, resulting in the synthesis of high-molecular-weight polymers with relatively narrow molecular-weight distribution. Previously unknown triamine 2 was synthesized by benzylation of HN(CH(2)CH(2)NHMes)(2) with benzyl chloride in the presence of K2CO3.
HPLC of Formula: C7H8O. About Benzyl Alcohol, If you have any questions, you can contact Mankaev, BN; Zaitsev, KV; Kuchuk, EA; Vershinina, MV; Zaitseva, GS; Egorov, MP; Karlov, SS or concate me.
Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles