A Tandem Ring Opening/Closure Reaction in A BF3 -Mediated Rearrangement of Spirooxindoles-Reference-Cited by-同舟云学术

A Tandem Ring Opening/Closure Reaction in A BF3 -Mediated Rearrangement of Spirooxindoles

Published:2017-10-16 Issue:24 Volume:359 Page:4393-4398
ISSN:1615-4150
Container-title:Advanced Synthesis & Catalysis
language:en
Short-container-title:Adv. Synth. Catal.

Author:

Guo Xuliang¹,Xing Qingyu¹,Lei Kunhua¹,Zhang-Negrerie Daisy¹,Du Yunfei¹²,Zhao Kang¹

Affiliation:

1. Tianjin Key Laboratory for Modern Drug Delivery & High-Efficiency; School of Pharmaceutical Science and Technology; Tianjin University; Tianjin 300072 People's Republic of China

2. Collaborative Innovation Center of Chemical Science and Engineering (Tianjin); Tianjin 300072 People's Republic of China

Funder

National Natural Science Foundation of China

National Basic Research Project

Tianjin Research Program of Application Foundation and Advanced Technology

Publisher

Wiley

Subject

General Chemistry

Reference68 articles.

1. A new synthetic procedure to spiro[cyclohexane-1,3′-indoline]-2′,4-diones

2. Concise Syntheses of (−)-Galanthamine and (±)-Codeine via Intramolecular Alkylation of a Phenol Derivative

3. Total Synthesis of (+)-3-Demethoxyerythratidinone and (+)-Erysotramidine via the Oxidative Amidation of a Phenol

4. Formal Total Syntheses of Aspidosperma Alkaloids via a Novel and General Synthetic Pathway Based on an Intramolecular Heck Cyclization

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