A Tandem Approach towards Diastereoselective Synthesis of Quinoline C‐3 Tethered γ‐Lactones,ChemistrySelect

当前位置： X-MOL 学术 › ChemistrySelect › 论文详情

Our official English website, www.x-mol.net, welcomes your feedback! (Note: you will need to create a separate account there.)

A Tandem Approach towards Diastereoselective Synthesis of Quinoline C‐3 Tethered γ‐Lactones
ChemistrySelect ( IF 1.9 ) Pub Date : 2018-01-09 , DOI: 10.1002/slct.201702923
Vipin Kumar ₁ , Sandeep Chaudhary ₂ , Manas Mathur ₃ , Ajit K. Swami ₃ , Chandi C. Malakar ₄ , Virender Singh ₁

Affiliation

A convenient approach has been developed for the facile synthesis of novel quinoline and α‐methylene γ‐butyrolactones based molecular hybrids. The tandem synthesis of quinoline C‐3 tethered lactone derivatives was achieved via indium‐mediated Barbier Type allylation followed by in situ intramolecular lactonisation approach.

中文翻译：