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Merck
CN
  • Enantioselective construction of functionalized thiopyrano-indole annulated heterocycles via a formal thio [3 + 3]-cyclization.

Enantioselective construction of functionalized thiopyrano-indole annulated heterocycles via a formal thio [3 + 3]-cyclization.

Organic letters (2014-12-18)
Xiang Chen, Zheng-Hang Qi, Shao-Yun Zhang, Ling-Pei Kong, Yong Wang, Xing-Wang Wang
摘要

A formal thio [3 + 3]-cyclization catalyzed by a DPEN-derived chiral thiourea has been reported for the construction of optically active thiopyrano-indole annulated heterocyclic compounds in high yields with excellent enantioselectivities. The high reactivity between indoline-2-thione (keto-S) and 2-benzylidenemalononitrile has also been supported by density functional theory (DFT) calculations.

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Sigma-Aldrich
硫脲, ACS reagent, ≥99.0%
Sigma-Aldrich
硫脲, ReagentPlus®, ≥99.0%
Sigma-Aldrich
1-Methylindoline-2-thione, ≥95%