TY  - JOUR
AU  - Tasovac, R.
AU  - Stefanović, Milutin
AU  - Stojiljković, A.
PY  - 1967
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4666
AB  - Reaction mechanism of diazoketone photolysie is assumed 
to involve the formation ofd-keto-carbene intermediates, final products being dependent on the molecular structure and 
reaction medium. Numerous example8 of Wolff-rearrangement (1) 
1,2-hydrogen shift (2) and intermolecular reactions (3) are available.
PB  - Elsevier
T2  - Tetrahedron Letters
T1  - Preparation and photolysis of 2-diazo-6-oximino- and 2,6-bisdiazo-4-tert. Butylcyclohexanone
VL  - 8
IS  - 28
SP  - 2729
EP  - 2732
DO  - 10.1016/S0040-4039(01)89983-4
ER  - 

@article{
author = "Tasovac, R. and Stefanović, Milutin and Stojiljković, A.",
year = "1967",
abstract = "Reaction mechanism of diazoketone photolysie is assumed 
to involve the formation ofd-keto-carbene intermediates, final products being dependent on the molecular structure and 
reaction medium. Numerous example8 of Wolff-rearrangement (1) 
1,2-hydrogen shift (2) and intermolecular reactions (3) are available.",
publisher = "Elsevier",
journal = "Tetrahedron Letters",
title = "Preparation and photolysis of 2-diazo-6-oximino- and 2,6-bisdiazo-4-tert. Butylcyclohexanone",
volume = "8",
number = "28",
pages = "2729-2732",
doi = "10.1016/S0040-4039(01)89983-4"
}

Tasovac, R., Stefanović, M.,& Stojiljković, A.. (1967). Preparation and photolysis of 2-diazo-6-oximino- and 2,6-bisdiazo-4-tert. Butylcyclohexanone. in Tetrahedron Letters
Elsevier., 8(28), 2729-2732.
https://doi.org/10.1016/S0040-4039(01)89983-4

Tasovac R, Stefanović M, Stojiljković A. Preparation and photolysis of 2-diazo-6-oximino- and 2,6-bisdiazo-4-tert. Butylcyclohexanone. in Tetrahedron Letters. 1967;8(28):2729-2732.
doi:10.1016/S0040-4039(01)89983-4 .

Tasovac, R., Stefanović, Milutin, Stojiljković, A., "Preparation and photolysis of 2-diazo-6-oximino- and 2,6-bisdiazo-4-tert. Butylcyclohexanone" in Tetrahedron Letters, 8, no. 28 (1967):2729-2732,
https://doi.org/10.1016/S0040-4039(01)89983-4 . .

TY  - JOUR
AU  - Mihailović, Milhailo Lj.
AU  - Stojiljković, A.
AU  - Andrejević, Vladimir
PY  - 1965
UR  - https://cer.ihtm.bg.ac.rs/handle/123456789/4655
AB  - The only amino compounds oxidized so far with lead tetroacetate were primary aromatic amines, which gave mainly the corresponding azo compounds(1), and some tertiary aryldialkyl amines, which in glacial acetic acid in the presence of acetic acid anhydride underwent oxidative dealkylation with the formation of acetylated secondary amines (2).
PB  - Elsevier
T2  - Tetrahedron Letters
T1  - The conversion of unbranched primary alkyl and arylalkyl amines to nitriles by means of lead tetraacetate
VL  - 6
IS  - 8
SP  - 461
EP  - 464
DO  - 10.1016/S0040-4039(00)89979-7
ER  - 

@article{
author = "Mihailović, Milhailo Lj. and Stojiljković, A. and Andrejević, Vladimir",
year = "1965",
abstract = "The only amino compounds oxidized so far with lead tetroacetate were primary aromatic amines, which gave mainly the corresponding azo compounds(1), and some tertiary aryldialkyl amines, which in glacial acetic acid in the presence of acetic acid anhydride underwent oxidative dealkylation with the formation of acetylated secondary amines (2).",
publisher = "Elsevier",
journal = "Tetrahedron Letters",
title = "The conversion of unbranched primary alkyl and arylalkyl amines to nitriles by means of lead tetraacetate",
volume = "6",
number = "8",
pages = "461-464",
doi = "10.1016/S0040-4039(00)89979-7"
}

Mihailović, M. Lj., Stojiljković, A.,& Andrejević, V.. (1965). The conversion of unbranched primary alkyl and arylalkyl amines to nitriles by means of lead tetraacetate. in Tetrahedron Letters
Elsevier., 6(8), 461-464.
https://doi.org/10.1016/S0040-4039(00)89979-7

Mihailović ML, Stojiljković A, Andrejević V. The conversion of unbranched primary alkyl and arylalkyl amines to nitriles by means of lead tetraacetate. in Tetrahedron Letters. 1965;6(8):461-464.
doi:10.1016/S0040-4039(00)89979-7 .

Mihailović, Milhailo Lj., Stojiljković, A., Andrejević, Vladimir, "The conversion of unbranched primary alkyl and arylalkyl amines to nitriles by means of lead tetraacetate" in Tetrahedron Letters, 6, no. 8 (1965):461-464,
https://doi.org/10.1016/S0040-4039(00)89979-7 . .