Indian Journal of Chemistry


Sect. B: Organic Chemistry including Medicinal Chemistry;

Total visitors: 6684 since 09-03-2012


VOL. 51B


March 2012




Rapid Communication







An enantiospecific synthesis of a crinipellin

Enantiospecific synthesis of a crinipellin, starting from campholenaldehyde has been described.










A Srikrishna* & V Gowri


Department of Organic Chemistry, Indian Institute of Science, Bangalore 560 012, India






















Synthesis of 5-oxo-1-substituted tetrazoles derived from amino acids


An application of amino acid derived isocyanates in the synthesis of 5-oxo-tetrazoles is described. The protocol has been extended for the insertion of tetrazolone in side chains of the Asp/Glu.






G Nagendra, N Narendra & Vommina V Sureshbabu*


aPeptide Research Laboratory, Department of Studies in Chemistry, Central College Campus, Bangalore University,
Dr B R Ambedkar Veedhi, Bangalore 560 001, India




















Synthesis and anticancer activity of 3,5-diaryl-1,2,4-oxadiazole derivatives


Condensation of chlorobenzamidoxime with chloro­s ubstituted benzoyl chloride gave 3,5 Diaryl-1,2,4-oxa­diazole derivatives in a single step. These were screened for their anticancer activity.











Mrityunjoy Kundu*, Jagadish Singh, Brijesh Singh, Tirtha Ghosh, B C Maiti & T K Maity


Institute of Pharmaceutical Sciences, Guru Ghasidas University, Bilaspur 495 009, India








AgOTf as an alternative catalyst for the regioselective cyclization of 2-(alkynyl)benzyl alcohols: Synthesis and biological evaluation of phthalans


The synthesized compounds have been studied for antimicrobial and anticancer activity.











Chandrasekaran Praveen, Chandran Iyyappan, Paramasivan T Perumal* & K Girija


Organic Chemistry Division, Central Leather Research Institute, Chennai 600 020, India




















Synthesis, characterization and antimicrobial screening of novel quinoline-thiazole derivatives









N C Desai*, Niraj Shihory, Kiran Rajpara & Amit Dodiya


Division of Medicinal Chemistry, Department of Chemistry, Mahatma Gandhi Campus, Bhavnagar University, Bhavnagar 364 002, India












Synthesis and antimicrobial activity of some new 3-chloro-6-substituted-N-(substituted 2H-[1,3]oxazino­[6,5-b]quinolin-3-(4H,5aH,9aH)-yl) benzo[b]thiophene-2-carboxamides


Some new 3-chloro-6-substituted-N-(6-substituted 2H-[1,3]Oxazino [6,5-b]quinolin-3-(4H,5aH,9aH)-yl)­benzo­[b]thiophene-2-carbox­ami­des have been synthe­sized and screened for their antimicrobial activity.









B V Guruprasad & B H M Mruthyunjayaswamy*


Department of Studies and Research in Chemistry. Gulbarga University, Gulbarga 585 106, India












Synthesis of new 2-(substituted)-5-methyl-2,3-di­hydro-1,3,2 λ5- benzoxazaphosphol-2-ones








C Venkateswarlu, P V V Satynarayana, C V Nageswara Rao* & C Naga Raju


Department of Chemistry, K V R College, Nandigama 521 185, India



























Microwave assisted green synthesis of novel spiro isoxazolidine derivatives with α-chloro nitrones


Microwave assisted 1,3-dipolar cycloaddition reaction of α-chloro nitrones to novel α-N-methyl and α-N-phenylfuran derivative affords exclusively single regioselective 5-spiro isoxazolidines while the same reaction with α-methylene-γ-butyrolactone affords two diastereomeric 5-spiro isoxazolidines with high selectivity.








Bhaskar Chakraborty* & Prawin Kumar Sharma


Organic Chemistry Laboratory, Sikkim Government College, Gangtok 737 102, India












Synthesis of 2-aryl-5-(benzofuran-2-yl)-thiazolo[3,2-b][1,2,4]triazoles using green procedures and their antibacterial activity


3-Aryl-5-(benzofuran-2-yl)acylthio-1,2,4-triazoles 1a-h on cyclisation using polyphosphoric acid under microwave irradiations give 2-aryl-5-(benzofuran-2-yl)-thiazolo[3,2-b][1,2,4]triazoles 2a-h. The antibacterial activity of these compounds has been described.







Komal Jakhar & J K Makrandi*


Department of Chemistry, Maharshi Dayanand University,  Rohtak 124 001, India
















One-pot, multicomponent synthesis of 4H-pyrano[2,3-c]pyrazoles in water at 25°C

Several pyranopyrazoles are synthesized by an iodine catalyzed four component reaction at 25°C in water. The yields are excellent; procedure is simple, efficient and environmentally benign.







M B Madhusudana Reddy & M A Pasha*


Department of Studies in Chemistry, Bangalore University, Central College Campus, Bengaluru 560 001, India








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