Glycerol as a recyclable solvent in a microwave-assisted synthesis of disulfides
Published 2011 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Glycerol as a recyclable solvent in a microwave-assisted synthesis of disulfides
Authors
Keywords
-
Journal
Green Chemistry Letters and Reviews
Volume 5, Issue 3, Pages 329-336
Publisher
Informa UK Limited
Online
2011-12-05
DOI
10.1080/17518253.2011.631942
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Catalyst-free synthesis of octahydroacridines using glycerol as recyclable solvent
- (2011) José E.R. Nascimento et al. TETRAHEDRON LETTERS
- Multicomponent Reactions of 1,3-Cyclohexanediones and Formaldehyde in Glycerol: Stabilization of Paraformaldehyde in Glycerol Resulted from using Dimedone as Substrate
- (2010) Minghao Li et al. ADVANCED SYNTHESIS & CATALYSIS
- Metal-Free Air Oxidation of Thiols in Recyclable Ionic Liquid: A Simple and Efficient Method for the Synthesis of Disulfides
- (2010) Devender Singh et al. EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
- Palladium-catalyzed cycloisomerization of (Z)-enynols into furans using green solvents: glycerol vs. water
- (2010) Javier Francos et al. GREEN CHEMISTRY
- Glycerol as a sustainable solvent for green chemistry
- (2010) Yanlong Gu et al. GREEN CHEMISTRY
- Glycerol eutectics as sustainable solvent systems
- (2010) Andrew P. Abbott et al. GREEN CHEMISTRY
- An Improved Method for the Synthesis of Disulfides by Periodic acid and Sodium Hydrogen Sulfite in Water
- (2010) Khalid M. Khan et al. LETTERS IN ORGANIC CHEMISTRY
- Ring-closing metathesis in glycerol under microwave activation
- (2010) Naoual Bakhrou et al. TETRAHEDRON LETTERS
- Glycerol as a promoting medium for cross-coupling reactions of diaryl diselenides with vinyl bromides
- (2010) Loren C. Gonçalves et al. TETRAHEDRON LETTERS
- Green, catalyst-free thioacetalization of carbonyl compounds using glycerol as recyclable solvent
- (2010) Gelson Perin et al. TETRAHEDRON LETTERS
- Synthesis of (Z)-organylthioenynes using KF/Al2O3/solvent as recyclable system
- (2010) Diego Alves et al. TETRAHEDRON LETTERS
- Base-free oxidation of thiols to disulfides using selenium ionic liquid
- (2010) Samuel Thurow et al. TETRAHEDRON LETTERS
- Bacterial production and refolding from inclusion bodies of a “Weak” toxin, a disulfide rich protein
- (2009) E. N. Lyukmanova et al. BIOCHEMISTRY-MOSCOW
- An Approach to Disulfide Synthesis Promoted by Sulfonyl Chloride in Sodium Bicarbonate Aqueous Media
- (2009) Huilong Xiao et al. PHOSPHORUS SULFUR AND SILICON AND THE RELATED ELEMENTS
- Green Route for Rapid Synthesis of 2,2′-Dithiobis(benzothiazole) by Microwave Irradiation
- (2009) Xin Wang et al. SYNTHETIC COMMUNICATIONS
- Electrochemical transformation of diazonium salts into diaryl disulfides
- (2009) Fructuoso Barba et al. TETRAHEDRON LETTERS
- KF/Al2O3 and PEG-400 as a recyclable medium for the selective α-selenation of aldehydes and ketones. Preparation of potential antimicrobial agents
- (2009) Francine Novack Victoria et al. TETRAHEDRON LETTERS
- Glycerin and CeCl3·7H2O: a new and efficient recyclable medium for the synthesis of bis(indolyl)methanes
- (2009) Claudio C. Silveira et al. TETRAHEDRON LETTERS
- Selenonium ionic liquid as efficient catalyst for the Baylis–Hillman reaction
- (2009) Eder J. Lenardão et al. TETRAHEDRON LETTERS
- Synthesis, DNA binding, and cytotoxic evaluation of new analogs of diallyldisulfide, an active principle of garlic
- (2008) Santosh Kumar Rai et al. BIOORGANIC & MEDICINAL CHEMISTRY
- Solvents from nature
- (2008) István T. Horváth GREEN CHEMISTRY
- Efficient synthesis of disulfides by air oxidation of thiols under sonication
- (2008) José Luis García Ruano et al. GREEN CHEMISTRY
Add your recorded webinar
Do you already have a recorded webinar? Grow your audience and get more views by easily listing your recording on Peeref.
Upload NowAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started