B. Senapati

ORCID: 0000-0002-2185-8896
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Research Areas
  • Agricultural pest management studies
  • Insect-Plant Interactions and Control
  • Genetic and Environmental Crop Studies
  • Insect Pest Control Strategies
  • Asymmetric Synthesis and Catalysis
  • Agricultural Practices and Plant Genetics
  • Agricultural Economics and Practices
  • Insect Resistance and Genetics
  • Synthetic Organic Chemistry Methods
  • Rice Cultivation and Yield Improvement
  • Agricultural Research and Practices
  • Crystallization and Solubility Studies
  • Peanut Plant Research Studies
  • Carbohydrate Chemistry and Synthesis
  • X-ray Diffraction in Crystallography
  • Cancer therapeutics and mechanisms
  • Bioactive Compounds and Antitumor Agents
  • Genetics and Plant Breeding
  • Traditional and Medicinal Uses of Annonaceae
  • Agricultural Science and Fertilization
  • Plant Virus Research Studies
  • Synthesis and Characterization of Pyrroles
  • Synthesis and Biological Activity
  • GABA and Rice Research
  • Oxidative Organic Chemistry Reactions

Midnapore Medical College and Hospital
2021-2023

Bidhan Chandra Krishi Viswavidyalaya
2004-2021

Leibniz-Institut für Naturstoff-Forschung und Infektionsbiologie e. V. - Hans-Knöll-Institut (HKI)
2021

A.E. Favorsky Irkutsk Institute of Chemistry
2021

Beijing University of Chemical Technology
2021

Kwangshin University
2009-2011

Sungkyunkwan University
2009-2010

Chungnam National University
2010

Korea Basic Science Institute
2010

Indian Institute of Technology Kharagpur
1995-2007

A catalytic route toward chiral Morita-Baylis-Hillman esters by asymmetric coupling between alpha,beta-acetylenic esters, aldehydes, and trimethylsilyl iodide has been developed (see scheme). The reaction proceeds with high to excellent enantioselectivities, the products can be transformed into beta-branched derivatives in a single step retention of configuration. TMS = trimethylsilyl.

10.1002/anie.200900351 article EN Angewandte Chemie International Edition 2009-05-04

A cationic oxazaborolidinium-catalyzed asymmetric Mukaiyama aldol reaction of (1-methoxy-2-methyl-propenyloxy)-trimethylsilane with various aldehydes including α,β-disubstituted acroleins has been developed in high yields and enantioselectivities. The synthetic utility this methodology was demonstrated the first short synthesis naturally occurring inthomycin C enantiopurity.

10.1021/ol102234k article EN Organic Letters 2010-10-19

The anionic [4+2] cycloaddition of furoindolones with arynes and quinol ethers is introduced as an efficient strategy for the synthesis indoloquinones. utility exemplified by a very short elipticine.

10.1055/s-2005-864826 article EN Synlett 2005-03-23

This review focuses on an overview of recent advances in the synthesis furanosteroids and illustrates their applications medicinal chemistry over period 2005–present.

10.1039/d0qo01454k article EN Organic Chemistry Frontiers 2021-01-01

Abstract Die katalytische asymmetrische Kupplung von α,β‐acetylenischen Estern mit Aldehyden und Trimethylsilyliodid führt zu chiralen Morita‐Baylis‐Hillman‐Estern (siehe Schema, TMS=Trimethylsilyl). Reaktion verläuft äußerst enantioselektiv, die Produkte lassen sich unter Erhaltung der Konfiguration in einem einzigen Schritt β‐verzweigte Derivate umwandeln. magnified image

10.1002/ange.200900351 article DE Angewandte Chemie 2009-05-04

SUMMARY Rice tungro disease (RTD), caused by the simultaneous infection of rice bacilliform virus (RTBV) and spherical (RTSV), is one major threats to sustainable production in South Southeast Asia. Transgenic resistance against RTBV has been reported previously using an RNA interference (RNAi) construct ( ORF IV RTBV, placed both sense anti-sense orientation under CaMV 35S promoter), scented line Pusa Basmati-1 (PB-1). This was transferred two high-yielding tungro-susceptible indica...

10.1017/s0021859611000827 article EN The Journal of Agricultural Science 2011-10-26

Genetic variances were estimated for grain yield and quality characters in rice (Oryza sativa L.) by full-sib half- sib analysis 20 F1 hybrids produced from crosses between five high yielding genotypes namely IR 50, 62, IET 5656, 8002 6441 as lines four Basmati 385, Dudheswar, Kalonunia Sambamahsuri testers. The significantly varying the characters, whereas due to testers significant all except panicle weight. Line × tester interaction was highly characters. Combining ability revealed...

10.56093/ijas.v82i4.16630 article EN cc-by-nc-sa The Indian Journal of Agricultural Sciences 2012-04-10

Herein, we report a rare pentacyclic N-fused hetrocycle synthesis via palladium catalyzed intramolecular C−H arylation along with the brief synthetic study of new type bicyclic/tricyclic pyrrole rings. This rings provided diversely substituted polycyclic nitrogen fused heterocycles from N-benzyl/N-benzyloxy pyrroles good to excellent yields.

10.1002/slct.201701800 article EN ChemistrySelect 2017-10-11

Journal Article Biology of the Mustard Aphid, Lipaphis erysimi, in India Get access G. Rout, Rout Orissa University Agriculture and Technology, Bhubaneswar-3, Search for other works by this author on: Oxford Academic Google Scholar B. Senapati Annals Entomological Society America, Volume 61, Issue 2, 15 March 1968, Pages 259–261, https://doi.org/10.1093/aesa/61.2.259 Published: 1968 history Accepted: 20 February 1967

10.1093/aesa/61.2.259 article EN Annals of the Entomological Society of America 1968-03-15

In the present work, Diels-Alder reaction of cyclopentadiene with ethylacrylate has been carried out by using two types mesoporous solid acid catalysts (Al-MCM-41, Al-MCM-48) different pore structures. The specific topology Al-MCM-48 (cubic Ia3d structure composed independent 3-D channel systems) exhibit higher activity and stereo-control than those Al-MCM-41 (hexagonal packing 1-D channels). physical properties catalyst, such as high accessibility reactants to sites, spatial confinement in...

10.5012/bkcs.2008.29.10.1993 article EN Bulletin of the Korean Chemical Society 2008-10-20

The preparation of several functionalized furan derivatives and attempts to transform them into a derivative containing 6H-furo[3,4-b]furanone skeleton towards the construction naphtho[2,3-b] are described. Attempted Pummerer reaction sulfoxide produced four interesting derivatives. Base promoted annulation between methyl 2-(phenylsulfinylmethyl)-3-furoate 2-cyclohexenone proceeded give dihydro naphtho[2,3-b]furanone in regiospecific manner.

10.4236/ijoc.2015.52008 article EN International Journal of Organic Chemistry 2015-01-01
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