C 2 -Symmetric 1,2-diamines are useful precursors to numerous reagents used in asymmetric synthesis and catalysis. We report here an efficient protocol for converting the two most commonly used trans-1,2-diamines to N,N-disubstituted derivatives, a transformation that simplifies the preparation of n
An efficient method for the synthesis of N,N′-dimethyl-1,2-diamines
✍ Scribed by Heather Tye; Colin Eldred; Martin Wills
- Publisher
- Elsevier Science
- Year
- 2002
- Tongue
- French
- Weight
- 153 KB
- Volume
- 43
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
A simple method for the preparation of N,N%-dimethyl-1,2-diamines is described. The method requires the dimethylation of a diazaphospholidine oxide followed by acid-catalysed hydrolysis.
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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
An enantioselective synthesis of C 2 -symmetric bis-homoallylic aromatic and heteroaromatic diamines in 54-89% yields, in 73-94% de and P98% ee has been achieved via the allylboration of the corresponding N,N 0 -bis(trimethylsilyl)dialdimines and N,N 0 -bis(diisobutylalumino)dialdimines with B-allyl