Scandium-catalyzed tandem selective oxirane ring-opening/Friedel–Crafts alkylation: a facile access to [1,4]oxazino[4,3-a]indoles and 3,4-dihydro-1H-pyrrolo[2,1-c][1,4]oxazines-Reference-Cited by-同舟云学术

Scandium-catalyzed tandem selective oxirane ring-opening/Friedel–Crafts alkylation: a facile access to [1,4]oxazino[4,3-a]indoles and 3,4-dihydro-1H-pyrrolo[2,1-c][1,4]oxazines

Published:2014-07-08 Issue:35 Volume:12 Page:6869
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Wei Lai,Liu Lu,Zhang Junliang

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2014/OB/C4OB01057D

Reference35 articles.

1. Practical Methodologies for the Synthesis of Indoles

2. Recent developments in indole ring synthesis—methodology and applications

3. Synthesis and Functionalization of Indoles Through Palladium-catalyzed Reactions

4. InBr3-Promoted Divergent Approach to Polysubstituted Indoles and Quinolines from 2-Ethynylanilines: Switch from an Intramolecular Cyclization to an Intermolecular Dimerization by a Type of Terminal Substituent Group

5. Synthesis, pharmacology and therapeutic potential of 10-methoxypyrazino[1,2-a]indoles, partial agonists at the 5HT2C receptor

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