Literature DB >> 16526812

Supramolecular catalysis of Strecker reaction in water under neutral conditions in the presence of beta-cyclodextrin.

K Surendra1, N Srilakshmi Krishnaveni, A Mahesh, K Rama Rao.   

Abstract

An environmentally benign and highly efficient procedure for the nucleophilic addition of trimethylsilyl cyanide to imines (Strecker reaction) has been developed under biomimetic conditions in water in the presence of beta-cyclodextrin to afford alpha-aminonitriles in quantitative yields. The use of cyclodextrin precludes the use of either acid or base, and the catalyst can be recycled a number of times without loss in activity.

Entities:  

Mesh:

Substances:

Year:  2006        PMID: 16526812     DOI: 10.1021/jo052510n

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  2 in total

1.  Efficient three-component Strecker reaction of aldehydes/ketones via NHC-amidate palladium(II) complex catalysis.

Authors:  Jamie Jarusiewicz; Yvonne Choe; Kyung Soo Yoo; Chan Pil Park; Kyung Woon Jung
Journal:  J Org Chem       Date:  2009-04-03       Impact factor: 4.354

2.  Gallium (III) triflate catalyzed efficient Strecker reaction of ketones and their fluorinated analogs.

Authors:  G K Surya Prakash; Thomas Mathew; Chiradeep Panja; Steevens Alconcel; Habiba Vaghoo; Clement Do; George A Olah
Journal:  Proc Natl Acad Sci U S A       Date:  2007-02-28       Impact factor: 11.205

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.