An Efficient and Facile Synthesis of 1-Alkyl-3,5-diaminobenzenes.
✍ Scribed by Sung Hoon Kim; Eun-Young Heo; Yong-Bae Kim
- Publisher
- John Wiley and Sons
- Year
- 2004
- Weight
- 104 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0931-7597
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract 3,5‐Dichloroaniline is commonly found in many compounds with pharmacological and other biological activities. [^13^C~6~]‐Aniline or its hydrochloride salt was converted in three steps to [^13^C~6~]‐3,5‐dichloroaniline, which can be incorporated in compounds of interest and used as inter
## Abstract magnified image 1‐Alkyl‐5‐arylalkoxy‐6‐methoxy‐3,4‐dihydroisoquinolines were synthesized by the alkylation of 1‐alkyl‐5‐hydroxy‐6‐methoxy‐3,4‐dihydroisoquinolines with arylalkyl halide in the presence of potassium carbonate. 1‐Alkyl‐5‐hydroxy‐6‐methoxy‐3,4‐dihydroisoquinolines as key p
## Abstract 1‐(Benzotriazol‐1‐yl)alkyl esters 2a‐u were obtained in yields averaging 86% by the direct reaction of various aldehydes with the corresponding __N__‐acylbenzotriazoles in the presence of a catalytic amount of potassium carbonate (10–25 mole %). The procedure was optimized by evaluating