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Refinado por: Base de dados/Biblioteca: DOAJ Directory of Open Access Journals remover assunto: Science & Technology remover
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1
Para amino benzoic acid-derived self-assembled biocompatible nanoparticles for efficient delivery of siRNA
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Para amino benzoic acid-derived self-assembled biocompatible nanoparticles for efficient delivery of siRNA

Reddy, Teegala Lakshminarayan ; Krishnarao, P Sivarama ; Rao, Garikapati Koteswara ; Bhimireddy, Eswar ; Venkateswarlu, P ; Mohapatra, Debendra K ; Yadav, J S ; Bhadra, Utpal ; Bhadra, Manika Pal

International journal of nanomedicine, 2015-01, Vol.10 (default), p.6411-6423 [Periódico revisado por pares]

New Zealand: Dove Medical Press Limited

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2
Mild and efficient conversion of aldehydes to gem-diacetates using 2nd generation ionic liquids
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Mild and efficient conversion of aldehydes to gem-diacetates using 2nd generation ionic liquids

Yadav, J.S. ; Reddy, B.V.S. ; Sreedhar, P. ; Kondaji, G. ; Nagaiah, K.

Catalysis communications, 2008-03, Vol.9 (5), p.590-593 [Periódico revisado por pares]

Elsevier B.V

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3
Amberlyst A-21®: An efficient, cost-effective and recyclable catalyst for the synthesis of substituted 4H-chromenes
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Amberlyst A-21®: An efficient, cost-effective and recyclable catalyst for the synthesis of substituted 4H-chromenes

Yadav, J.S. ; Reddy, B.V. Subba ; Gupta, Manoj K. ; Prathap, I. ; Pandey, S.K.

Catalysis communications, 2007-12, Vol.8 (12), p.2208-2211 [Periódico revisado por pares]

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4
PMA/SiO2 catalyzed amidation of alcohols with nitriles: A simple, cost-effective and recyclable catalytic system for Ritter reaction
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PMA/SiO2 catalyzed amidation of alcohols with nitriles: A simple, cost-effective and recyclable catalytic system for Ritter reaction

Yadav, J.S. ; Subba Reddy, B.V. ; Pandurangam, T. ; Jayasudan Reddy, Y. ; Gupta, Manoj K.

Catalysis communications, 2008-03, Vol.9 (6), p.1297-1301 [Periódico revisado por pares]

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5
The silver salt of 12-tungstophosphoric acid: A mild and selective catalyst for the synthesis of β-ketoesters via C–H insertion
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The silver salt of 12-tungstophosphoric acid: A mild and selective catalyst for the synthesis of β-ketoesters via C–H insertion

Yadav, J.S. ; Subba Reddy, B.V. ; Purnima, K.V. ; Jhansi, S. ; Nagaiah, K. ; Lingaiah, N.

Catalysis communications, 2008-08, Vol.9 (14), p.2361-2364 [Periódico revisado por pares]

Elsevier B.V

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6
LiClO4-catalyzed cleavage of aziridines with thiols: A facile synthesis of β-aminosulfides
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LiClO4-catalyzed cleavage of aziridines with thiols: A facile synthesis of β-aminosulfides

Yadav, J.S. ; Reddy, B.V.S. ; Baishya, G. ; Venkatram Reddy, P. ; Narsaiah, A.V.

Catalysis communications, 2006-10, Vol.7 (10), p.807-810 [Periódico revisado por pares]

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7
Montmorillonite KSF/SiO2 as novel and recyclable solid acids for the synthesis of β-aminohalides and β-azidoamines
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Montmorillonite KSF/SiO2 as novel and recyclable solid acids for the synthesis of β-aminohalides and β-azidoamines

Yadav, J.S ; Reddy, B.V.S ; Sadashiv, K ; Raghavendra, S ; Harikishan, K

Catalysis communications, 2004-03, Vol.5 (3), p.111-114 [Periódico revisado por pares]

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8
Occurrence of neo-XY system in Tryxalis indica Thunb
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Occurrence of neo-XY system in Tryxalis indica Thunb

Yadav, J.S ; Karamjeet ; Yadav, A.S

Caryologia, 1981, Vol.34 (3), p.311-316 [Periódico revisado por pares]

Taylor & Francis

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9
Facile Synthesis of 9,10-Dihydro-4H-Benzo [4,5] Cyclohepta [1,2-b] Thiophene-4-One: A Crucial Drug Intermediate-Application of Wittig-Horner Reaction
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Facile Synthesis of 9,10-Dihydro-4H-Benzo [4,5] Cyclohepta [1,2-b] Thiophene-4-One: A Crucial Drug Intermediate-Application of Wittig-Horner Reaction

Murty, M.S.R. ; Ramalingam, T. ; Sabitha, G. ; Yadav, J.S.

Heterocyclic communications, 2001, Vol.7 (5), p.449-454 [Periódico revisado por pares]

De Gruyter

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10
FACILE SYNTHESIS OF 3-(THIOPHENOXY/PHENOXY)- 4-PHENYL-1,2-DIHYDRO-2-QUINOLINONES
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FACILE SYNTHESIS OF 3-(THIOPHENOXY/PHENOXY)- 4-PHENYL-1,2-DIHYDRO-2-QUINOLINONES

Yadav, J.S. ; Reddy, E.J. ; Madhavi, G. ; Ramalingam, T.

Heterocyclic communications, 2000, Vol.6 (5), p.403-408 [Periódico revisado por pares]

De Gruyter

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