化学
咪唑啉受体
戒指(化学)
范围(计算机科学)
分子内力
基质(水族馆)
锂(药物)
组合化学
甲苯
立体化学
有机化学
药理学
程序设计语言
内分泌学
地质学
海洋学
医学
计算机科学
作者
Mikhail Krasavin,Sergey Grintsevich,Alexander Sapegin
出处
期刊:Synthesis
[Georg Thieme Verlag KG]
日期:2022-02-10
卷期号:54 (10): 2494-2510
被引量:5
标识
DOI:10.1055/s-0040-1719882
摘要
Abstract Substrates that are insufficiently activated towards the hydrated imidazoline ring expansion (HIRE) process have been previously found to deliver exclusively the products of aminoalkyl side-chain ring expansion. Attempted reversal of the process by thermal activation towards HIRE failed. We have found that for such problematic substrates the HIRE-type ring expansion can be effectively achieved by applying lithium hexamethyldisilazide (LHMDS) in toluene. LHMDS is thought to promote intramolecular transamidation, which leads to ring-expanded 10- and 11-membered heterocyclic products in modest to good yields. The process significantly broadens the substrate scope amenable to the HIRE strategy.
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