DFT Study on the Mechanism of Amides to Aldehydes Using Cp2Zr(H)Cl-Reference-Cited by-同舟云学术

DFT Study on the Mechanism of Amides to Aldehydes Using Cp2Zr(H)Cl

Published:2009-12-15 Issue:1 Volume:29 Page:42-51
ISSN:0276-7333
Container-title:Organometallics
language:en
Short-container-title:Organometallics

Author:

Wang Juping¹²,Xu Huiying¹,Gao Hui¹,Su Cheng-Yong¹,Zhao Cunyuan¹,Phillips David Lee³

Affiliation:

1. MOE Laboratory of Bioinorganic and Synthetic Chemistry, School of Chemistry and Chemical Engineering, Sun Yat-Sen University, Guangzhou 510275, People's Republic of China

2. School of Pharmacy, Guangdong Pharmaceutical University, People's Republic of China

3. Department of Chemistry, The University of Hong Kong, Pokfulam Road, Hong Kong, People's Republic of China

Publisher

American Chemical Society (ACS)

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/om900371u

Reference62 articles.

1. Chemical Synthesis of Natural Product Peptides: Coupling Methods for the Incorporation of Noncoded Amino Acids into Peptides

2. Selective Reductions. V. The Partial Reduction of Tertiary Amides by Lithium Di- and Triethoxyaluminohydrides-A New Aldehyde Synthesis via the Dimethylamides

3. LITHIUM DIETHOXYALUMINOHYDRIDE AS A SELECTIVE REDUCING AGENT—THE REDUCTION OF DIMETHYLAMIDES TO ALDEHYDES

4. A new synthesis of aldehydes from acids via reduction of N-acyl saccharins using sodium dihydro bis-(2-methoxy-ethoxy) aluminate

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