Nitrogen containing privileged structures and their solid phase combinatorial synthesis

Amit Verma1, Mange Ram Yadav, Rajani Giridhar

  • 1Pharmacy Department, Faculty of Technology & Engineering, The M S University of Baroda, Kala Bhavan, Vadodara-390001, Gujarat, India.

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Chirality at Nitrogen, Phosphorus, and Sulfur

Chirality is most prevalent in carbon-based tetrahedral compounds, but this important facet of molecular symmetry extends to sp3-hybridized nitrogen, phosphorus and sulfur centers, including trivalent molecules with lone pairs. Here, the lone pair behaves as a functional group in addition to the other three substituents to form an analogous tetrahedral center that can be chiral.
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One of the common methods to prepare nitriles is the dehydration of amides. This method requires strong dehydrating agents like phosphorous pentoxide or boiling acetic anhydride for converting amides to nitriles. Another reagent namely, thionyl chloride also accomplishes the dehydration of amides, where amide acts as a nucleophile. The first step of the mechanism involves the nucleophilic attack by the amide on the thionyl chloride to form an intermediate. In the next step, the electron pairs...
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Isomerism in Complexes
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Structure of Carboxylic Acid Derivatives
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