Department of Chemistry and Fujian Provincial Key Laboratory of Chemical Biology, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen, Fujian 361005, P. R. China.
J Org Chem. 2021 Dec 3;86(23):16300-16314. doi: 10.1021/acs.joc.1c01572. Epub 2021 Sep 9.
Ten types of TfO/TTBP-mediated amide transformation reactions were investigated. The results showed that compared with pyridine derivatives 2,6-di--butyl-4-methylpyridine (DTBMP) and 2-fluoropyridine (2-F-Pyr.), TTBP can serve as an alternative amide activation system for the direct transformation of both secondary and tertiary amides. For most surveyed examples, higher or comparable yields were generally obtained. In addition, TfO/TTBP combination was used to promote the condensation reactions of 2-(-butyldimethylsilyloxy)furan (TBSOF) with both tertiary and secondary amides, the one-pot reductive Bischler-Napieralski-type reaction of tertiary lactams, and Movassaghi and Hill's modern version of the Bischler-Napieralski reaction. The value of the TfO/TTBP-based methodology was further demonstrated by the concise and high-yielding syntheses of several natural products.
研究了十种 TfO/TTBP 介导的酰胺转化反应。结果表明,与吡啶衍生物 2,6-二--丁基-4-甲基吡啶(DTBMP)和 2-氟吡啶(2-F-Pyr.)相比,TTBP 可以作为仲酰胺和叔酰胺直接转化的替代酰胺活化体系。对于大多数调查的例子,通常可以获得更高或相当的产率。此外,TfO/TTBP 组合还用于促进 2-(-丁基二甲基甲硅氧基)呋喃(TBSOF)与叔酰胺和仲酰胺的缩合反应、叔内酰胺的一锅还原 Bischler-Napieralski 型反应,以及 Movassaghi 和 Hill 的 Bischler-Napieralski 反应的现代版本。TfO/TTBP 基方法的价值还通过几种天然产物的简洁高产合成得到了进一步证明。