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Search for "drug development" in Full Text gives 102 result(s) in Beilstein Journal of Organic Chemistry.

Identification and synthesis of impurities formed during sertindole preparation

  • I. V. Sunil Kumar,
  • G. S. R. Anjaneyulu and
  • V. Hima Bindu

Beilstein J. Org. Chem. 2011, 7, 29–33, doi:10.3762/bjoc.7.5

Graphical Abstract
  • , quantification, and control of impurities in the drug substance and drug product are important parts of drug development for obtaining marketing approval. It is more challenging for an organic chemist to identify the impurities which are formed in very small quantities in a drug substance. Since most of the time
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Published 07 Jan 2011

The subtle balance of weak supramolecular interactions: The hierarchy of halogen and hydrogen bonds in haloanilinium and halopyridinium salts

  • Kari Raatikainen,
  • Massimo Cametti and
  • Kari Rissanen

Beilstein J. Org. Chem. 2010, 6, No. 4, doi:10.3762/bjoc.6.4

Graphical Abstract
  • systems and its potential in drug development has also been recognized [22]. The halogen bond (XB), whose terminology emphasizes the similarity with hydrogen bonding [23] can be schematically described by Y–X···A, where X is the XB donor atom (Lewis acid, electrophilic) and A is the XB acceptor atom
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Published 15 Jan 2010
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