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Govind Ballabh Pant University of Agriculture and Technology, Pantnagar

After independence, development of the rural sector was considered the primary concern of the Government of India. In 1949, with the appointment of the Radhakrishnan University Education Commission, imparting of agricultural education through the setting up of rural universities became the focal point. Later, in 1954 an Indo-American team led by Dr. K.R. Damle, the Vice-President of ICAR, was constituted that arrived at the idea of establishing a Rural University on the land-grant pattern of USA. As a consequence a contract between the Government of India, the Technical Cooperation Mission and some land-grant universities of USA, was signed to promote agricultural education in the country. The US universities included the universities of Tennessee, the Ohio State University, the Kansas State University, The University of Illinois, the Pennsylvania State University and the University of Missouri. The task of assisting Uttar Pradesh in establishing an agricultural university was assigned to the University of Illinois which signed a contract in 1959 to establish an agricultural University in the State. Dean, H.W. Hannah, of the University of Illinois prepared a blueprint for a Rural University to be set up at the Tarai State Farm in the district Nainital, UP. In the initial stage the University of Illinois also offered the services of its scientists and teachers. Thus, in 1960, the first agricultural university of India, UP Agricultural University, came into being by an Act of legislation, UP Act XI-V of 1958. The Act was later amended under UP Universities Re-enactment and Amendment Act 1972 and the University was rechristened as Govind Ballabh Pant University of Agriculture and Technology keeping in view the contributions of Pt. Govind Ballabh Pant, the then Chief Minister of UP. The University was dedicated to the Nation by the first Prime Minister of India Pt Jawaharlal Nehru on 17 November 1960. The G.B. Pant University is a symbol of successful partnership between India and the United States. The establishment of this university brought about a revolution in agricultural education, research and extension. It paved the way for setting up of 31 other agricultural universities in the country.

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  • ThesisItemOpen Access
    Green Synthesis, derivatization and structure - activity relationships of bioactive compounds as potential antioxidants and enzyme inhibitors
    (G.B. Pant University of Agriculture and Technology, Pantnagar-263145 (Uttarakhand), 2015-06) Agarwal, Deepali; Kasana, Virendra
    Derivatives of formamide, α-aminophosphonate, 3,4-dihydropyrimidin-2(1H)- one and naphthoquinone were synthesised using green synthetic methods. Calcium chloride dihydrate supported on rice husk (RiH-CaCl2.2H2O) offers simple, efficient and economical solid support method for C-N bond formation for N-formylation of amines at room temperature. Natural acid catalysts, lemon juice (extracted from Citrus limonium) and yogurt (bacterial fermented milk), were developed for one pot synthesis of α-aminophosphonates and amino acid derivatives of α-aminophosphonate under solvent free condition. CaCl2.2H2O offers efficient method for direct carbon-carbon bond formation through soft enolization to promote the Biginelli three component condensation reaction from a diversity of aromatic aldehydes. N-formylated α- aminophosphonate and 3,4-dihydropyrimidin-2(1H)-one derivatives were synthesized using β-cyclodextrin in the presence of ionic liquid, TBAB, in good to excellent yield. Novel derivative of 1, 4-Naphthoquinone was synthesized in excellent yield as pH indicator and chemosensor for Sn2+, Hg2+ and Zn2+. Citrulline and tyrosine derivatives of α-aminophosphonate and compounds with -OH, -OCH3 substituent groups on benzene ring of α-aminophosphonates and 3,4-dihydropyrimidin-2(1H)-ones showed strong antioxidant and enzyme (tyrosinase, α-amylase and α-glucosidase) inhibition activity. N-formylation increased the antioxidant and enzyme inhibition activity of α- aminophosphonates and 3,4-dihydropyrimidin-2(1H)-ones with para -NO2 and -F groups on benzene ring. N-formylated 3,4-dihydropyrimidin-2(1H)-ones were found to increase the Fe2+ chelating activity.