Weinreb amide as an efficient reagent in the one pot synthesis of benzimidazoles and benzothiazoles-Reference-Cited by-同舟云学术

Weinreb amide as an efficient reagent in the one pot synthesis of benzimidazoles and benzothiazoles

Published:2013-05 Issue:21 Volume:54 Page:2693-2695
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Bommegowda Yadaganahalli K.,Lingaraju Gejjalagere S.,Thamas Saji,Vinay Kumar Koravangala S.,Pradeepa Kumara Challanayakanahally S.,Rangappa Kanchugarakoppal S.,Sadashiva Marilinganadoddi P.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference64 articles.

1. Imidazolyl benzimidazoles and imidazo[4,5-b]pyridines as potent p38α MAP kinase inhibitors with excellent in vivo antiinflammatory properties

2. Synthesis, antibacterial, antifungal activity and interaction of CT-DNA with a new benzimidazole derived Cu(II) complex

3. Antihelminthic activity of some newly synthesized 5(6)-(un)substituted-1H-benzimidazol-2-ylthioacetylpiperazine derivatives

4. Synthesis and Angiotensin II Receptor Antagonistic Activities of Benzimidazole Derivatives Bearing Acidic Heterocycles as Novel Tetrazole Bioisosteres

5. Opioid operant self-administration, analgesia, stimulation and respiratory depression inμ-deficient mice

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