ChemInform Abstract: Broensted Acid-Catalyzed Nazarov Cyclization of Pyrrole Derivatives Accelerated by Microwave Irradiation.

ChemInform ◽  
2009 ◽  
Vol 40 (48) ◽  
Author(s):  
Prabhakar Bachu ◽  
Takahiko Akiyama
Holzforschung ◽  
2018 ◽  
Vol 72 (12) ◽  
pp. 1025-1030
Author(s):  
Mafuyu Saito ◽  
Takao Kishimoto ◽  
Masahiro Hamada ◽  
Noriyuki Nakajima ◽  
Daisuke Urabe

AbstractConversion of lignocellulose into useful chemicals is an important research topic in the area of biomass utilization. In this study, microcrystalline cellulose (MC) was dissolved in a mixed-solvent system containing the ionic liquid (IL) 1-allyl-3-methylimidazolium chloride ([Amim]Cl) andN-methyl-pyrrolidone (NMP), and the cellulose was directly converted into methyl glucoside (MG) by acid-catalyzed methanolysis aided by microwave irradiation (μWIr). Under moderate reaction temperature and pressure, and in the presence of acetyl chloride/methanol (in situformed HCl) as an acid catalyst, MG was obtained in a 42% yield. In contrast, in the absence of either IL or μWIr, the MG yield was only 5 or 21%, respectively. Both μWIr and the dissolution of cellulose in IL were quite effective for the conversion of cellulose into MG.


2013 ◽  
Vol 2013 ◽  
pp. 1-6 ◽  
Author(s):  
Feray Aydogan ◽  
Cigdem Yolacan

A new procedure to synthesize the N-substituted pyrrole derivatives by Clauson Kaas reaction catalyzed by acidic ionic liquid under microwave irradiation was developed. This procedure provides several advantages such as high yield, clean product formation, and short reaction time.


ChemInform ◽  
2013 ◽  
Vol 44 (10) ◽  
pp. no-no
Author(s):  
Sadiya Raja ◽  
Winai Ieawsuwan ◽  
Vadim Korotkov ◽  
Magnus Rueping

2012 ◽  
Vol 9 (5) ◽  
pp. 791-798 ◽  
Author(s):  
R. Ghanbaripour ◽  
I. Mohammadpoor-Baltork ◽  
M. Moghadam ◽  
A. R. Khosropour ◽  
S. Tangestaninejad ◽  
...  

2012 ◽  
Vol 7 (10) ◽  
pp. 2361-2366 ◽  
Author(s):  
Sadiya Raja ◽  
Winai Ieawsuwan ◽  
Vadim Korotkov ◽  
Magnus Rueping

ChemInform ◽  
2009 ◽  
Vol 40 (37) ◽  
Author(s):  
J. Venu Madhav ◽  
Y. Thirupathi Reddy ◽  
P. Narsimha Reddy ◽  
Peter A. Crooks ◽  
V. Naveen Kumar ◽  
...  

Synfacts ◽  
2007 ◽  
Vol 2007 (4) ◽  
pp. 0432-0432
Author(s):  
M. Rueping ◽  
W. Ieawsuwan ◽  
A. Antonchick ◽  
B. Nachtsheim

Synthesis ◽  
2020 ◽  
Vol 52 (14) ◽  
pp. 2045-2064 ◽  
Author(s):  
Puthiyaparambath Sharathna ◽  
Murugan Thulasi Meenu ◽  
Kokkuvayil Vasu Radhakrishnan ◽  
Bhandara Purayil Dhanya ◽  
Greeshma Gopalan ◽  
...  

We herein disclose an effective strategy for the synthesis of [5.3.0] and [6.3.0] fused polycyclic terpenoids, which are important structural elements of natural products and biologically active compounds. The method comprises of Lewis acid catalyzed interrupted Nazarov cyclization of zerumbone derivatives such as zerumbone epoxide, triazole-appended zerumbone, zerumbal, and zerumbenone with a wide substrate scope with different indoles. Zerumbone epoxide furnished [5.3.0] and [6.3.0] fused structurally diverse sesquiterpenoids and all other zerumbone derivatives furnished the [6.3.0] fused motifs.


RSC Advances ◽  
2016 ◽  
Vol 6 (8) ◽  
pp. 6138-6143 ◽  
Author(s):  
Elina Marinho ◽  
M. Fernanda Proença

The hydrochloride salt of 2-(2-aminophenyl)quinazoline-4-amine, prepared from a quinazolino[3,4-a]quinazoline, was reacted with aromatic aldehydes under conventional heating or microwave irradiation, leading to tetracyclic dihydroquinazolines.


Sign in / Sign up

Export Citation Format

Share Document