textjournal article
Efficient Microwave-Assisted Synthesis of Unsymmetrical Disulfides
Abstract
An efficient synthesis of unsymmetrical disulfides exemplified for cysteines and penicillamines is described. The use of dimethyl sulfoxide mediated oxidation accelerated by microwave irradiation afforded various unsymmetrical disulfides in one step and in high yields- Text
- Journal contribution
- Biophysics
- Biochemistry
- Neuroscience
- Physiology
- Mental Health
- Plant Biology
- Virology
- Biological Sciences not elsewhere classified
- Physical Sciences not elsewhere classified
- irradiation
- Efficient
- unsymmetrical disulfides
- dimethyl
- sulfoxide
- synthesis
- penicillamine
- oxidation
- DisulfidesAn
- Unsymmetrical
- yield
- cysteine
- Synthesi
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Last time updated on 16/03/2018
This paper was published in The Francis Crick Institute.
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