Literature DB >> 29137490

Recent developments concerning the application of the Mannich reaction for drug design.

Bernhard Biersack1, Khursheed Ahmed2, Subhash Padhye3, Rainer Schobert1.   

Abstract

INTRODUCTION: The versatile multicomponent Mannich reaction occupies a salient position in organic chemistry and drug design. Sound knowledge of its scope and variations and of the biological activities of Mannich bases is crucial for the development and improvement of drugs for various diseases. Areas covered: The following article provides an overview of the latest developments in the field of drugs based on the Mannich reaction. Web-based literature searching tools such as PubMed and SciFinder were applied to obtain useful articles. In addition, pertinent literature that was recently published by the authors is discussed in this manuscript. The chemical structures of bioactive Mannich bases are also given. Expert opinion: The Mannich reaction represents a feasible and cost-effective procedure with great potential for drug development. Several newly discovered Mannich bases exhibit sound activities against various human diseases as well as favorable pharmacokinetics. Thus, scientific research about Mannich bases is prospering and appears very attractive both for chemists and for clinicians.

Entities:  

Keywords:  Aminoalkylation; Mannich bases; Mannich reaction; bioavailability; drug design; multicomponent reaction

Mesh:

Substances:

Year:  2017        PMID: 29137490     DOI: 10.1080/17460441.2018.1403420

Source DB:  PubMed          Journal:  Expert Opin Drug Discov        ISSN: 1746-0441            Impact factor:   6.098


  5 in total

Review 1.  Catalytic stereoselective Mannich-type reactions for construction of fluorinated compounds.

Authors:  Minoo Dabiri; Noushin Farajinia Lehi; Reza Mohammadian
Journal:  Mol Divers       Date:  2021-07-06       Impact factor: 2.943

2.  Stereodivergent access to all four stereoisomers of chiral tetrahydrobenzo[f][1,4]oxazepines, through highly diastereoselective multicomponent Ugi-Joullié reaction.

Authors:  Alessandro Pinna; Andrea Basso; Chiara Lambruschini; Lisa Moni; Renata Riva; Valeria Rocca; Luca Banfi
Journal:  RSC Adv       Date:  2020-01-03       Impact factor: 3.361

3.  Hf(OTf)4-Catalyzed Three-Component Synthesis of N-Carbamate-Protected β-Amino Ketones.

Authors:  Zhen-Zhen Chen; Dong-Zhao Yang; Ying-Ying Dong; Mei Chi; Shou-Zhi Pu; Qi Sun
Journal:  Molecules       Date:  2022-02-08       Impact factor: 4.411

4.  Synthesis of 4-Hydroxyquinolines as Potential Cytotoxic Agents.

Authors:  Oszkár Csuvik; Nikoletta Szemerédi; Gabriella Spengler; István Szatmári
Journal:  Int J Mol Sci       Date:  2022-08-26       Impact factor: 6.208

5.  Leveraging Electron-Deficient Iminium Intermediates in a General Synthesis of Valuable Amines.

Authors:  Che-Sheng Hsu; Carlos R Gonçalves; Veronica Tona; Amandine Pons; Marcel Kaiser; Nuno Maulide
Journal:  Angew Chem Int Ed Engl       Date:  2022-03-16       Impact factor: 16.823

  5 in total

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