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11
Total synthesis of Z-isomer of phomolide B
Total synthesis of Z-isomer of phomolide B
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Total synthesis of Z-isomer of phomolide B

Mohapatra, Debendra K. ; Reddy, D. Prabhakar ; Dash, Uttam ; Yadav, J.S.

Tetrahedron letters, 2011-01, Vol.52 (1), p.151-154 [Periódico revisado por pares]

Elsevier Ltd

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12
Stereoselective syntheses of (−)-tetrahydrolipstatin via Prins cyclisations
Stereoselective syntheses of (−)-tetrahydrolipstatin via Prins cyclisations
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Stereoselective syntheses of (−)-tetrahydrolipstatin via Prins cyclisations

Yadav, J.S. ; Reddy, M. Sridhar ; Prasad, A.R.

Tetrahedron letters, 2006-07, Vol.47 (29), p.4995-4998 [Periódico revisado por pares]

Elsevier Ltd

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13
One-pot three-component coupling reaction: solvent-free synthesis of novel 3-substituted indoles catalyzed by PMA–SiO2
One-pot three-component coupling reaction: solvent-free synthesis of novel 3-substituted indoles catalyzed by PMA–SiO2
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One-pot three-component coupling reaction: solvent-free synthesis of novel 3-substituted indoles catalyzed by PMA–SiO2

Srihari, P. ; Singh, Vinay K. ; Bhunia, Dinesh C. ; Yadav, J.S.

Tetrahedron letters, 2009-07, Vol.50 (27), p.3763-3766 [Periódico revisado por pares]

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14
Application of the Cosford cross-coupling protocol for the stereoselective synthesis of ( R)-(+)-goniothalamin, ( R)-(+)-kavain and ( S)-(+)-7,8-dihydrokavain
Application of the Cosford cross-coupling protocol for the stereoselective synthesis of ( R)-(+)-goniothalamin, ( R)-(+)-kavain and ( S)-(+)-7,8-dihydrokavain
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Application of the Cosford cross-coupling protocol for the stereoselective synthesis of ( R)-(+)-goniothalamin, ( R)-(+)-kavain and ( S)-(+)-7,8-dihydrokavain

Sabitha, Gowravaram ; Sudhakar, K. ; Yadav, J.S.

Tetrahedron letters, 2006-11, Vol.47 (48), p.8599-8602 [Periódico revisado por pares]

Elsevier Ltd

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15
A carbohydrate approach for the synthesis of tetrahydropyran containing C16–C29 fragment of sorangicin A
A carbohydrate approach for the synthesis of tetrahydropyran containing C16–C29 fragment of sorangicin A
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A carbohydrate approach for the synthesis of tetrahydropyran containing C16–C29 fragment of sorangicin A

Srihari, P. ; Kumaraswamy, B. ; Yadav, J.S.

Tetrahedron, 2009-08, Vol.65 (32), p.6304-6309 [Periódico revisado por pares]

Kidlington: Elsevier Ltd

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16
Solvent-free NbCl5 catalyzed condensation of 1,3-dicarbonyl compounds and aldehydes: a facile synthesis of trisubstituted alkenes
Solvent-free NbCl5 catalyzed condensation of 1,3-dicarbonyl compounds and aldehydes: a facile synthesis of trisubstituted alkenes
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Solvent-free NbCl5 catalyzed condensation of 1,3-dicarbonyl compounds and aldehydes: a facile synthesis of trisubstituted alkenes

Yadav, J.S. ; Bhunia, Dinesh C. ; Singh, Vinay K. ; Srihari, P.

Tetrahedron letters, 2009-05, Vol.50 (21), p.2470-2473 [Periódico revisado por pares]

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17
Stereoselective formal synthesis of aspergillide A
Stereoselective formal synthesis of aspergillide A
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Stereoselective formal synthesis of aspergillide A

Sabitha, Gowravaram ; Vasudeva Reddy, D. ; Senkara Rao, A. ; Yadav, J.S.

Tetrahedron letters, 2010-08, Vol.51 (32), p.4195-4198 [Periódico revisado por pares]

Elsevier Ltd

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18
Stereoselective synthesis of methyl branched chiral deoxypropionate units: a new route for synthesis of insect pheromone (−)-lardolure and (2R,4R,6R,8R) 2,4,6,8-tetramethylundecanoic acid
Stereoselective synthesis of methyl branched chiral deoxypropionate units: a new route for synthesis of insect pheromone (−)-lardolure and (2R,4R,6R,8R) 2,4,6,8-tetramethylundecanoic acid
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Stereoselective synthesis of methyl branched chiral deoxypropionate units: a new route for synthesis of insect pheromone (−)-lardolure and (2R,4R,6R,8R) 2,4,6,8-tetramethylundecanoic acid

Yadav, J.S. ; Sengupta, Sandip ; Yadav, Nagendra Nath ; Narasimha Chary, D. ; Al Ghamdi, Ahmad Alkhazim

Tetrahedron letters, 2012-10, Vol.53 (44), p.5952-5954 [Periódico revisado por pares]

Elsevier Ltd

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19
First total syntheses and absolute configuration of rugulactone and 6(R)-(4′-oxopent-2′-enyl)-5,6-dihydro-2H-pyran-2-one
First total syntheses and absolute configuration of rugulactone and 6(R)-(4′-oxopent-2′-enyl)-5,6-dihydro-2H-pyran-2-one
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First total syntheses and absolute configuration of rugulactone and 6(R)-(4′-oxopent-2′-enyl)-5,6-dihydro-2H-pyran-2-one

Mohapatra, Debendra K. ; Das, Pragna P. ; Sai Reddy, D. ; Yadav, J.S.

Tetrahedron letters, 2009-10, Vol.50 (43), p.5941-5944 [Periódico revisado por pares]

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20
Stereoselective synthesis of anti-1,3-diol units via Prins cyclisation: application to the synthesis of (−)-sedamine
Stereoselective synthesis of anti-1,3-diol units via Prins cyclisation: application to the synthesis of (−)-sedamine
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Stereoselective synthesis of anti-1,3-diol units via Prins cyclisation: application to the synthesis of (−)-sedamine

Yadav, J.S. ; Reddy, M. Sridhar ; Rao, P. Purushothama ; Prasad, A.R.

Tetrahedron letters, 2006-06, Vol.47 (26), p.4397-4401 [Periódico revisado por pares]

Elsevier Ltd

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