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Process for the preparation of cephalosporins

Deshpande, Pandurang Balwant (Chennai, IN) R1 represents hydrogen, trityl, CH3, CRaRbCOORc CH2OCOCH3, CH═CH2, CH2OCONH2, 21 which

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Santhanagopalan, Chithra (Chennai, IN) R1 is selected from O, S or together with suitable groups represented by D include CH2 or

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Structure and conformation of n- (t-butoxycarbonyl

20031016-(2) 8542(2) 9120(2) 9501(2) 9681(2) 8690 University of Madras, Chennai-600 025, India (R1 and wR2 are 0.0659 and 0.1654,

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Process for the preparation of cephalosporin intermediate and

(I), activating the 4-halogeno-2-substituted Ganesh, Praveen Nagesh (Chennai, IN) (II) wherein R1 represents CH3, CRaRbCOORc

Structure and conformation of n- (t-butoxycarbonyl

20031016-(2) 8542(2) 9120(2) 9501(2) 9681(2) 8690 University of Madras, Chennai-600 025, India (R1 and wR2 are 0.0659 and 0.1654,

Process for the preparation of 3-propenyl cephalosporin DMF

Konda, Ramesh Athmaram (Chennai, IN) (IX) wherein R1 represents a carboxy protecting a halogenated solvent and a base at a

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Process for the preparation of 3-propenyl cephalosporin DMF

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Levamisole, Avermectins or similar in pyrrolidone solvent

Indira Nagar, Adya, Chennai 0 Tamilnadu, 600at least 2 actives wherein a first of the Month Month /3 7°C/3 7°C/3 7°C R1

Levamisole, Avermectins or similar in pyrrolidone solvent

Indira Nagar, Adya, Chennai 0 Tamilnadu, 600at least 2 actives wherein a first of the Month Month /3 7°C/3 7°C/3 7°C R1

Novel 2-substituted methyl penam derivatives

Devarajan, Sathishkumar (Chennai, IN) R1 represents carboxylate anion, or —COOR4 .2.0]hept-3-yl]methyl}-3-methyl-1H-1,2,3

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Novel MAO-A inhibitors

Santhanagopalan, Chithra (Chennai, IN) R1 is selected from O, S or together with suitable groups represented by D include CH2 or

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