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Bioorganic and Medicinal Chemistry Letters

Volumn 22, Issue 24, 2012, Pages 7418-7421

A regio- and stereoselective 1,3-dipolar cycloaddition for the synthesis of new-fangled dispiropyrrolothiazoles as antimycobacterial agents

(8) Almansour, Abdulrahman I a Ali, Sadath d Ali, Mohamed Ashraf b,c,d Ismail, Rusli b Choon, Tan Soo b Sellappan, Velmurugan d Elumalai, Karthi Keyan d Pandian, Suresh d

a KING SAUD UNIVERSITY (Saudi Arabia)

b INSTITUTE FOR RESEARCH IN MOLECULAR MEDICINE INFORMM (Malaysia)

c Alwar Pharmacy College (India)

d Sunrise University (India)

Author keywords

1,3 Dipolar cycloaddition; Antimycobacterial; Azomethine ylide; Dispiro; Indanone; Intermolecular

Indexed keywords

ANTIMYCOBACTERIAL AGENT; DISPIROPYRROLOTHIAZOLE DERIVATIVE; UNCLASSIFIED DRUG;

ANTIBACTERIAL ACTIVITY; ARTICLE; BACTERIAL STRAIN; CHEMISTRY; CYCLOADDITION; DRUG STRUCTURE; DRUG SYNTHESIS; MINIMUM INHIBITORY CONCENTRATION; MYCOBACTERIUM TUBERCULOSIS; NONHUMAN; REGIOSELECTIVITY; STEREOCHEMISTRY;

ANTI-BACTERIAL AGENTS; CYCLIZATION; DOSE-RESPONSE RELATIONSHIP, DRUG; MICROBIAL SENSITIVITY TESTS; MOLECULAR STRUCTURE; MYCOBACTERIUM TUBERCULOSIS; PYRROLES; STEREOISOMERISM; STRUCTURE-ACTIVITY RELATIONSHIP; THIAZOLES;

MYCOBACTERIUM TUBERCULOSIS;

EID: 84870252483 PISSN: 0960894X EISSN: 14643405 Source Type: Journal
DOI: 10.1016/j.bmcl.2012.10.059 Document Type: Article

Times cited : (21)

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