One-pot and highly regio-selective 1,3-dipole cycloaddition of azomethine ylide generated in situ to tetraethyl vinylidenebisphosphonate (VBP) catalyzed by cerium(iv) oxide-Reference-Cited by-同舟云学术

One-pot and highly regio-selective 1,3-dipole cycloaddition of azomethine ylide generated in situ to tetraethyl vinylidenebisphosphonate (VBP) catalyzed by cerium(iv) oxide

Published:2014 Issue:8 Volume:38 Page:3350-3353
ISSN:1144-0546
Container-title:New J. Chem.
language:en
Short-container-title:New J. Chem.

Author:

Li Guozhu¹²³⁴,Wu Mingshu¹²³⁴,Kong Dulin¹²³⁴,Liu Rendie¹²³⁴,Zhou Xueming¹²³⁴,Liu Fengjiao¹²³⁴

Affiliation:

1. Key Laboratory of Tropical Medicinal Plant Chemistry of the Ministry of Education

2. College of Chemistry & Chemical Engineering

3. Hainan Normal University

4. Haikou 571158, P. R. China

Abstract

Higly regio-selective heterocyclic bisphosphonates are obtained in moderate yields (30–70%). The structures of the targeted molecules are characterized by NMR (such as COSY, HSQC, and HMBC), IR and MS.

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2014/NJ/C4NJ00558A

Reference32 articles.

1. Catalytic Enantioselective 1,3-Dipolar Cycloadditions of Azomethine Ylides for Biology-Oriented Synthesis

2. Regio- and Stereoselective Synthesis of Novel Dispiropyrrolidine Bisoxindole Derivatives via Multicomponent Reactions

3. Regioselective Synthesis of Novel Spiropyrrolidines and Spirothiapyrrolizidines Through Multicomponent 1,3-Dipolar Cycloaddition Reaction of Azomethine Ylides

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