Cu(II)-Macrocylic [H4]Salen Catalyzed Asymmetric Nitroaldol Reaction and Its Application in the Synthesis of α1-Adrenergic Receptor Agonist (R)-Phenylephrine-Reference-Cited by-同舟云学术

Cu(II)-Macrocylic [H4]Salen Catalyzed Asymmetric Nitroaldol Reaction and Its Application in the Synthesis of α1-Adrenergic Receptor Agonist (R)-Phenylephrine

Published:2011-10-12 Issue:11 Volume:1 Page:1529-1535
ISSN:2155-5435
Container-title:ACS Catalysis
language:en
Short-container-title:ACS Catal.

Author:

Kureshy Rukhsana I.¹,Das Anjan¹,Khan Noor-ul H.¹,Abdi Sayed H. R.¹,Bajaj Hari C.¹

Affiliation:

1. Discipline of Inorganic Materials and Catalysis, Central Salt and Marine Chemicals Research Institute (CSIR-CSMCRI), Bhavnagar 364 021, Gujarat, India

Publisher

American Chemical Society (ACS)

Subject

Catalysis,General Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/cs2004467

Reference68 articles.

1. Recent Advances in the Catalytic Asymmetric Nitroaldol (Henry) Reaction

2. Effect of Ligand Structure on the Zinc-Catalyzed Henry Reaction. Asymmetric Syntheses of (−)-Denopamine and (−)-Arbutamine

3. Highly enantioselective nitroaldol reaction catalyzed by new chiral copper complexes

4. The Nitro Group in Organic Synthesis

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