A Cost-Efficient Synthesis of Simvastatin via High-Conversion Methylation of an Alkoxide Ester Enolate von Thaper, Rajesh K, Kumar, Yatendra, Dileep Kumar, S. M, Misra, Satyananda, Khanna, Jag Mohan

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An Efficient Method for the Reduction of Cephalosporin Sulfoxides von Tewari, Neera, Kumar, Yatendra, Thaper, Rajesh Kumar, Khanna, Jag Mohan

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Use of a Novel Reagent in the Synthesis of 3-Exomethylenecephams von Thaper, Rajesh K., Kumar, Yatendra, Khanna, Jag Mohan

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Process for producing pure form of 2-methyl-4-(4-methyl-1-piperazinyl)-10H-thieno[2,3-b][1,5]benzodiazepine von BHATNAGAR AKSHAT, THAPER RAJESH K, SHASTRI JWALANT A, DUBEY SUSHIL K

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Process for producing pure form of 2-methyl-4-(4-methyl-1-piperazinyl)-10H-thieno[2,3-b][1,5]benzodiazepine von Shastri, Jwalant A, Bhatnagar, Akshat, Thaper, Rajesh K, Dubey, Sushil K

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ChemInform Abstract: A Cost-Efficient Synthesis of Simvastatin via High-Conversion Methylation of an Alkoxide Ester Enolate von Thaper, Rajesh K., Kumar, Yatendra, Kumar, S. M. Dileep, Misra, Satyananda, Khanna, Jag Mohan

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KEY INTERMEDIATES IN THE MANUFACTURE OF SIMVASTATINE von KHANNA JAG M, MISRA SATYANANDA, THAPER RAJESH K, KUMAR YATENDRA, KUMAR S. M. DILEP

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Process for manufacturing simvastatin from lovastatin or mevinolinic acid von S. M. DILEEP KUMAR, YATENDRA KUMAR, RAJESH K. THAPER, SATYANANDA MISRA, JAG M. KHANNA

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Key intermediates in the manufacture of simvastatin von S. M. DILEEP KUMAR, YATENDRA KUMAR, RAJESH K. THAPER, SATYANANDA MISRA, JAG M. KHANNA

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Polymorphs, Salts, and Cocrystals: What’s in a Name? von Aitipamula, Srinivasulu, Banerjee, Rahul, Bansal, Arvind K, Biradha, Kumar, Cheney, Miranda L, Choudhury, Angshuman Roy, Desiraju, Gautam R, Dikundwar, Amol G, Dubey, Ritesh, Duggirala, Nagakiran, Ghogale, Preetam P, Ghosh, Soumyajit, Goswami, Pramod Kumar, Goud, N. Rajesh, Jetti, Ram R. K. R, Karpinski, Piotr, Kaushik, Poonam, Kumar, Dinesh, Kumar, Vineet, Moulton, Brian, Mukherjee, Arijit, Mukherjee, Gargi, Myerson, Allan S, Puri, Vibha, Ramanan, Arunachalam, Rajamannar, T, Reddy, C. Malla, Rodriguez-Hornedo, Nair, Rogers, Robin D, Row, T. N. Guru, Sanphui, Palash, Shan, Ning, Shete, Ganesh, Singh, Amit, Sun, Changquan C, Swift, Jennifer A, Thaimattam, Ram, Thakur, Tejender S, Kumar Thaper, Rajesh, Thomas, Sajesh P, Tothadi, Srinu, Vangala, Venu R, Variankaval, Narayan, Vishweshwar, Peddy, Weyna, David R, Zaworotko, Michael J

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Correction for Polymorphs, Salts and Cocrystals: What’s in a Name? von Aitipamula, Srinivasulu, Banerjee, Rahul, Bansal, Arvind K, Biradha, Kumar, Cheney, Miranda L, Choudhury, Angshuman Roy, Desiraju, Gautam R, Dikundwar, Amol G, Dubey, Ritesh, Duggirala, Nagakiran, Ghogale, Preetam P, Ghosh, Soumyajit, Goswami, Pramod Kumar, Goud, N. Rajesh, Jetti, Ram K. R, Karpinski, Piotr, Kaushik, Poonam, Kumar, Dinesh, Kumar, Vineet, Moulton, Brian, Mukherjee, Arijit, Mukherjee, Gargi, Myerson, Allan S, Puri, Vibha, Ramanan, Arunachalam, Rajamannar, T, Reddy, C. Malla, Rodriguez-Hornedo, Nair, Rogers, Robin D, Row, T. N. Guru, Sanphui, Palash, Shan, Ning, Shete, Ganesh, Singh, Amit, Sun, Changquan C, Swift, Jennifer A, Thaimattam, Ram, Thakur, Tejender S, Kumar Thaper, Rajesh, Thomas, Sajesh P, Tothadi, Srinu, Vangala, Venu R, Vishweshwar, Peddy, Weyna, David R, Zaworotko, Michael J

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Structure of (22S)-3β-acetoxy-20-(3-isopropylisoxazolin-5-yl)-4,4,14α-trimethylpregn-8(9)-ene von Lindeman, S. V., Alexanyan, M. S., Struchkov, Yu. T., Kumar Thaper, R., Reshetova, I. G., Kamernitzky, A. V.

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Process for Lactonization in the Preparation of Statins von KHANNA JAG M, SINGH GOVIND, BHADWAL PARAMVIR, PANCHASARA DINESH R, JAISWAL SANJAY, THAPER RAJESH T, DUBEY SUSHIL K

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