Asset Details
MbrlCatalogueTitleDetail
Do you wish to reserve the book?
Base-Controlled Regiospecific Mono-Benzylation/Allylation and Diallylation of 4-Aryl-5-indolyl-1,2,4-triazole-3-thione: Thio-Aza Allyl Rearrangement
by
Soliman, Saied M.
, Barakat, Assem
, Youssef, Mohamed F.
, Haukka, Matti
, Salama, Eid E.
, Sarhan, Ahmed A. M.
, Boraei, Ahmed T. A.
in
1,2,4-triazole-3-thione
/ Allyl compounds
/ allylation
/ Aromatic compounds
/ Biological activity
/ Cancer
/ Chemical reactions
/ Crystallization
/ Diffraction
/ Maraviroc
/ Nitrogen
/ NMR
/ Nuclear magnetic resonance
/ Single crystals
/ Sulfur
/ Sulfur compounds
/ thio-aza allyl rearrangement
/ Triazoles
/ Unit cell
/ X-ray single-crystal analysis
/ X-rays
2023
Hey, we have placed the reservation for you!
By the way, why not check out events that you can attend while you pick your title.
You are currently in the queue to collect this book. You will be notified once it is your turn to collect the book.
Oops! Something went wrong.
Looks like we were not able to place the reservation. Kindly try again later.
Are you sure you want to remove the book from the shelf?
Base-Controlled Regiospecific Mono-Benzylation/Allylation and Diallylation of 4-Aryl-5-indolyl-1,2,4-triazole-3-thione: Thio-Aza Allyl Rearrangement
by
Soliman, Saied M.
, Barakat, Assem
, Youssef, Mohamed F.
, Haukka, Matti
, Salama, Eid E.
, Sarhan, Ahmed A. M.
, Boraei, Ahmed T. A.
in
1,2,4-triazole-3-thione
/ Allyl compounds
/ allylation
/ Aromatic compounds
/ Biological activity
/ Cancer
/ Chemical reactions
/ Crystallization
/ Diffraction
/ Maraviroc
/ Nitrogen
/ NMR
/ Nuclear magnetic resonance
/ Single crystals
/ Sulfur
/ Sulfur compounds
/ thio-aza allyl rearrangement
/ Triazoles
/ Unit cell
/ X-ray single-crystal analysis
/ X-rays
2023
Oops! Something went wrong.
While trying to remove the title from your shelf something went wrong :( Kindly try again later!
Do you wish to request the book?
Base-Controlled Regiospecific Mono-Benzylation/Allylation and Diallylation of 4-Aryl-5-indolyl-1,2,4-triazole-3-thione: Thio-Aza Allyl Rearrangement
by
Soliman, Saied M.
, Barakat, Assem
, Youssef, Mohamed F.
, Haukka, Matti
, Salama, Eid E.
, Sarhan, Ahmed A. M.
, Boraei, Ahmed T. A.
in
1,2,4-triazole-3-thione
/ Allyl compounds
/ allylation
/ Aromatic compounds
/ Biological activity
/ Cancer
/ Chemical reactions
/ Crystallization
/ Diffraction
/ Maraviroc
/ Nitrogen
/ NMR
/ Nuclear magnetic resonance
/ Single crystals
/ Sulfur
/ Sulfur compounds
/ thio-aza allyl rearrangement
/ Triazoles
/ Unit cell
/ X-ray single-crystal analysis
/ X-rays
2023
Please be aware that the book you have requested cannot be checked out. If you would like to checkout this book, you can reserve another copy
We have requested the book for you!
Your request is successful and it will be processed during the Library working hours. Please check the status of your request in My Requests.
Oops! Something went wrong.
Looks like we were not able to place your request. Kindly try again later.
Base-Controlled Regiospecific Mono-Benzylation/Allylation and Diallylation of 4-Aryl-5-indolyl-1,2,4-triazole-3-thione: Thio-Aza Allyl Rearrangement
Journal Article
Base-Controlled Regiospecific Mono-Benzylation/Allylation and Diallylation of 4-Aryl-5-indolyl-1,2,4-triazole-3-thione: Thio-Aza Allyl Rearrangement
2023
Request Book From Autostore
and Choose the Collection Method
Overview
The regiospecific S-benzylation/allylation of two 4-aryl-5-indolyl-1,2,4-triazole-3-thione precursors was carried out using Et3N as a base. Allyl group migration from exocyclic sulfur to the triazole nitrogen (N3) was successfully achieved in a short time via thermal fusion without the need for any catalyst. The allylation of indole nitrogen, along with exocyclic sulfur or triazole nitrogen (N3), was carried out using K2CO3 as stronger base. S,N-Diallylated products were converted to N,N-diallylated analogues using a simple fusion approach. Structural analyses of the two newly synthesized hybrids 2b and 5b investigated via the X-ray diffraction of a single crystal combined with Hirshfeld calculations. The compound 5b was crystallized in a monoclinic crystal system and the P21/c space group, whereas in compound 2b, the crystal system comprises the less symmetric triclinic and P − 1 space group. The asymmetric unit contains one and two molecules of 5b and 2b, respectively, while the unit cell contains four molecules in both cases. Hirshfeld analysis was performed in both systems to analyze the non-covalent interactions that control molecular packing. For 5b, C…H, N…H, S…H, Cl…N and H…H interactions are the most significant. Their percentages are 23.7, 8.8, 4.5, 1.2 and 48.2, respectively. In the case of 2b, the Cl…C, S…N, C…H, H…H and N…H interactions have the upper hand in molecular packing. In one unit, the percentages of these contacts are 2.3, 0.9, 26.8, 38.7 and 9.3%, while in the other unit, the corresponding values are 4.4, 1.3, 22.1, 43.6 and 9.0%, respectively.
Publisher
MDPI AG
Subject
MBRLCatalogueRelatedBooks
Related Items
Related Items
This website uses cookies to ensure you get the best experience on our website.