ChemInform Abstract: Triisopropylsilyl Protected Hexa-1,5-diyne-3,4-dione: A Convenient Precursor to 2,3-Dialkynyl 1,4-Diazabutadienes.
โ Scribed by R. FAUST; B. GOEBELT; C. WEBER
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 35 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0931-7597
No coin nor oath required. For personal study only.
โฆ Synopsis
In view of the interest in the synthesis of diimine-ligated transition metal complexes as components of efficient catalyst systems, a new method for the preparation of 1,4-diazabutadienes is developed. Starting from silyl-protected dialkynyl-1,2-dione (I) they are easily accessible by reaction with excess anilines.
๐ SIMILAR VOLUMES
Bis [1,2]dithiolo [3,4-b][4',3'-e][1,4]thiazine-3,5-dione, a Planar 1,4-Thiazine. -Reaction of N-benzyldiisopropylamine (I) with S 2 Cl 2 gives N-benzyl-bisthiolothiazine (II) with typically folded structure. Debenzylation of (II) results in a dramatic flattening of the molecule structure giving th