Faculty of Chemistry Repository - Cherry
University of Belgrade - Faculty of Chemistry
    • English
    • Српски
    • Српски (Serbia)
  • English 
    • English
    • Serbian (Cyrillic)
    • Serbian (Latin)
  • Login
View Item 
  •   Cherry
  • Hemijski fakultet
  • Publikacije
  • View Item
  •   Cherry
  • Hemijski fakultet
  • Publikacije
  • View Item
JavaScript is disabled for your browser. Some features of this site may not work without it.

A novel m-CPBA oxidation: p-quinols and epoxyquinols from phenols

Authorized Users Only
1996
Authors
Šolaja, Bogdan A.
Milić, Dragana
Gasic, MJ
Article (Published version)
Metadata
Show full item record
Abstract
Steroidal quinols were obtained on large scale in 50-57% yield, together with syn-epoxyquinols. The reaction conditions can be adjusted to afford only the corresponding steroidal epoxyquinol in 51-54% yield. Copyright (C) 1996 Elsevier Science Ltd
Source:
Tetrahedron Letters, 1996, 37, 21, 3765-3768
Publisher:
  • Pergamon-Elsevier Science Ltd, Oxford

DOI: 10.1016/0040-4039(96)00677-6

ISSN: 0040-4039

WoS: A1996UN05600042

Scopus: 2-s2.0-0029976484
[ Google Scholar ]
23
22
URI
https://cherry.chem.bg.ac.rs/handle/123456789/2241
Collections
  • Publikacije
Institution/Community
Hemijski fakultet
TY  - JOUR
AU  - Šolaja, Bogdan A.
AU  - Milić, Dragana
AU  - Gasic, MJ
PY  - 1996
UR  - https://cherry.chem.bg.ac.rs/handle/123456789/2241
AB  - Steroidal quinols were obtained on large scale in 50-57% yield, together with syn-epoxyquinols. The reaction conditions can be adjusted to afford only the corresponding steroidal epoxyquinol in 51-54% yield. Copyright (C) 1996 Elsevier Science Ltd
PB  - Pergamon-Elsevier Science Ltd, Oxford
T2  - Tetrahedron Letters
T1  - A novel m-CPBA oxidation: p-quinols and epoxyquinols from phenols
VL  - 37
IS  - 21
SP  - 3765
EP  - 3768
DO  - 10.1016/0040-4039(96)00677-6
UR  - Kon_3572
ER  - 
@article{
author = "Šolaja, Bogdan A. and Milić, Dragana and Gasic, MJ",
year = "1996",
abstract = "Steroidal quinols were obtained on large scale in 50-57% yield, together with syn-epoxyquinols. The reaction conditions can be adjusted to afford only the corresponding steroidal epoxyquinol in 51-54% yield. Copyright (C) 1996 Elsevier Science Ltd",
publisher = "Pergamon-Elsevier Science Ltd, Oxford",
journal = "Tetrahedron Letters",
title = "A novel m-CPBA oxidation: p-quinols and epoxyquinols from phenols",
volume = "37",
number = "21",
pages = "3765-3768",
doi = "10.1016/0040-4039(96)00677-6",
url = "Kon_3572"
}
Šolaja, B. A., Milić, D.,& Gasic, M.. (1996). A novel m-CPBA oxidation: p-quinols and epoxyquinols from phenols. in Tetrahedron Letters
Pergamon-Elsevier Science Ltd, Oxford., 37(21), 3765-3768.
https://doi.org/10.1016/0040-4039(96)00677-6
Kon_3572
Šolaja BA, Milić D, Gasic M. A novel m-CPBA oxidation: p-quinols and epoxyquinols from phenols. in Tetrahedron Letters. 1996;37(21):3765-3768.
doi:10.1016/0040-4039(96)00677-6
Kon_3572 .
Šolaja, Bogdan A., Milić, Dragana, Gasic, MJ, "A novel m-CPBA oxidation: p-quinols and epoxyquinols from phenols" in Tetrahedron Letters, 37, no. 21 (1996):3765-3768,
https://doi.org/10.1016/0040-4039(96)00677-6 .,
Kon_3572 .

DSpace software copyright © 2002-2015  DuraSpace
About CHERRY - CHEmistry RepositoRY | Send Feedback

re3dataOpenAIRERCUB
 

 

All of DSpaceInstitutions/communitiesAuthorsTitlesSubjectsThis institutionAuthorsTitlesSubjects

Statistics

View Usage Statistics

DSpace software copyright © 2002-2015  DuraSpace
About CHERRY - CHEmistry RepositoRY | Send Feedback

re3dataOpenAIRERCUB