CER - Central Repository
Institute of Chemistry, Technology and Metallurgy
    • English
    • Српски
    • Српски (Serbia)
  • English 
    • English
    • Serbian (Cyrillic)
    • Serbian (Latin)
  • Login
View Item 
  •   CER
  • IHTM
  • Radovi istraživača / Researchers' publications
  • View Item
  •   CER
  • IHTM
  • Radovi istraživača / Researchers' publications
  • View Item
JavaScript is disabled for your browser. Some features of this site may not work without it.

Preparation and photolysis of 2-diazo-6-oximino- and 2,6-bisdiazo-4-tert. Butylcyclohexanone

Authorized Users Only
1967
Authors
Tasovac, R.
Stefanović, Milutin
Stojiljković, A.
Article (Published version)
Metadata
Show full item record
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.
Keywords:
photolysis of 2-diazo-6-oximino- and 2,6-bisdiazo-4-tert / Butylcyclohexanone / photolysie / molecular structure / hydrogen / intermolecular reaction
Source:
Tetrahedron Letters, 1967, 8, 28, 2729-2732
Publisher:
  • Elsevier

DOI: 10.1016/S0040-4039(01)89983-4

ISSN: 0040-4039; 1873-3581

Scopus: 2-s2.0-0005760829
[ Google Scholar ]
6
URI
https://cer.ihtm.bg.ac.rs/handle/123456789/4666
Collections
  • Radovi istraživača / Researchers' publications
Institution/Community
IHTM
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 . .

DSpace software copyright © 2002-2015  DuraSpace
About CeR – Central Repository | Send Feedback

re3dataOpenAIRERCUB
 

 

All of DSpaceInstitutions/communitiesAuthorsTitlesSubjectsThis institutionAuthorsTitlesSubjects

Statistics

View Usage Statistics

DSpace software copyright © 2002-2015  DuraSpace
About CeR – Central Repository | Send Feedback

re3dataOpenAIRERCUB