Half-sandwich rare-earth metal tris(alkyl) ate complexes catalyzed phosphaguanylation reaction of phosphines with carbodiimides: an efficient synthesis of phosphaguanidines-Reference-Cited by-同舟云学术

Half-sandwich rare-earth metal tris(alkyl) ate complexes catalyzed phosphaguanylation reaction of phosphines with carbodiimides: an efficient synthesis of phosphaguanidines

Published:2015 Issue:10 Volume:39 Page:7649-7655
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Ma Wangyang¹²³⁴⁵,Xu Ling¹²³⁴⁵,Zhang Wen-Xiong¹²³⁴⁵,Xi Zhenfeng¹²³⁴⁵

Affiliation:

1. Beijing National Laboratory for Molecular Sciences

2. MOE Key Laboratory of Bioorganic Chemistry and Molecular Engineering

3. College of Chemistry

4. Peking University

5. Beijing 100871

Abstract

Half-sandwich Y/Li ate complex displays better catalytic activity for phosphaguanylation reaction of phosphines with carbodiimides than the neutral yttrium complexes.

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2015/NJ/C5NJ01136A

Reference56 articles.

1. Mechanistic Considerations of the Catalytic Guanylation Reaction of Amines with Carbodiimides for Guanidine Synthesis

2. Recent development of synthetic preparation methods for guanidines via transition metal catalysis

3. Guanidines: from classical approaches to efficient catalytic syntheses

4. Titanacarborane mediated C–N bond forming/breaking reactions

5. Catalytic addition of alkyne C–H, amine N–H, and phosphine P–H bonds to carbodiimides: an efficient route to propiolamidines, guanidines, and phosphaguanidines

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