## 1, 3, 2, fide 1 reacts with substituted 2-amino-1,4-naphthoquinons 2a-d to give 4,5,4Π,5Π-benzodiphenoquinonebis-1,3,2-thiazaphospholine-2-sulfide derivatives of type 3. Compatible analytical and spectroscopic results were obtained for all the new compounds. A mechanism is proposed to explain t
β¦ LIBER β¦
Novel 2-Amino-3-(2,4-dinitrophenylamino) Derivatives of 1,4-Naphthoquinone.
β Scribed by Thida Win; Shmuel Bittner
- Publisher
- John Wiley and Sons
- Year
- 2005
- Weight
- 16 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0931-7597
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## Abstract Sulfenylchlorides, sulfenates, and sulfenamides of 1,4βnaphthoquinone were synthesized, and different methods of their syntheses were investigated. Synthesized sulfenates and sulfenamides are stable due to the large electronβwithdrawing potential of the conjugated quinonic system. Obtai