14525-98-5Relevant academic research and scientific papers
New synthesis of diazepino[3,2,1-ij]quinoline and pyrido[1,2,3-de] quinoxalines via addition-elimination followed by cycloacylation
Baraldi, Pier Giovanni,Ruggiero, Emanuela,Tabrizi, Mojgan Aghazadeh
, p. 101 - 105 (2014/02/14)
This paper describes a convenient and efficient synthesis of new fused tricyclic diazepino[3,2,1-ij]quinolines and substituted pyrido[1,2,3-de] quinoxalines. o-Phenylenediamines are transformed in the tricycle nucleus in only a few-step synthetic sequence
Heterocyclic dialdehydes: Linkers in the synthesis of macroacyclic ligands
Kudyakova,Burgart,Saloutin
experimental part, p. 558 - 563 (2012/01/13)
Macroacyclic heteroatomic podands containing one chelation cavity were obtained as a result of the biscondensation of diethyl 2-[(2-aminophenyl) aminomethylidene]malonate with heterocyclic dialdehy- des (2,5- thiophenedicarbaldehyde and 2,6-pyridinedicarb
2,2-Bis(ethoxycarbonyl)vinyl (BECV) as a versatile amine protecting group for selective functional-group transformations
Ilangovan, Andivelu,Kumar, Rajendran Ganesh
supporting information; experimental part, p. 2938 - 2943 (2010/07/02)
A 2,2-Bis(ethoxycarbonyl) vinyl- (BECV) group was used for the selective protection of amines at room temperature in the presence of potentially interfering functional groups such as OH, SH, COOH as well as other NH 2 groups. Several functional group transformations such as esterification, O-alkylation, O-acylation, N-alkylation, N-acylation, S-alkylation can selectively be carried out in the presence of the BECV group. The selective deprotection of the BECV group was achieved in a short time using ethylenediamine at room temperature while several other functional groups such as benzoate, aliphatic esters, amides and ethers remain intact. The BECV group shows orthogonal stability against the common protecting groups such as Fmoc, Cbz and Boc.
