2-Mercaptobenzothiazolylmethylpyrrole as a new means for the synthesis of pyrromethanes under neutral conditions
✍ Scribed by Kunisuke Okada; Kiyoshi Saburi; Keishi Nomura; Hideo Tanino
- Book ID
- 104258961
- Publisher
- Elsevier Science
- Year
- 1998
- Tongue
- French
- Weight
- 158 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
lXe coupling reaction of 2-mercaptobenzothiazolyhnethylpyrrole 4b with a-free pyrrole 2b in the presence of silver (l) triflate proceeds smoothly at room tempemture to give pyrromethane lb in excellent yield 4b reacts rapidly with pyrromethane lb undo similar neutml conditions to afford symmetric pyrromethane 7 in preparative yield.
📜 SIMILAR VOLUMES
Magtrieve TM can be used for the deprotection of acetals and ketals or for the direct oxidation to carboxylic acids under neutral conditions.
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