Prabhakar Sunchu | Indian Institute of Chemical Technology (original) (raw)
Synthetic organic chemist with working knowledge in total synthesis of natural products , medicinal analogues, carbohydrates, nucleotides, bio-catalysis and homogeneous and heterogeneous catalysis and looking for opportunity
Address: Hyderabad, Andhra Pradesh, India
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Papers by Prabhakar Sunchu
Tetrahedron Letters, 2013
Tetrahedron Letters, 2013
Tetrahedron Letters, 2012
European Journal of Organic Chemistry, Nov 30, 2023
RSC Adv., 2015
Triazine-aryl-bis-indole derivative inhibits phosphodiesterase activity.
RSC Advances, 2013
The first stereoselective total synthesis of the Z-isomer of (6S,7R,9R)-6,7-dihydroxy-9-propylnon... more The first stereoselective total synthesis of the Z-isomer of (6S,7R,9R)-6,7-dihydroxy-9-propylnon-4-eno-9lactone involving Sharpless titanium(IV) mediated regioselective ring-opening reaction, Steglich esterification and RCM as the key steps is reported.
Herein we report the first stereoselective total synthesis of phomonol via Sharpless asymmetric d... more Herein we report the first stereoselective total synthesis of phomonol via Sharpless asymmetric dihydroxylation and 6-exo-trig oxa-Michael addition as the key steps.
Herein the first total synthesis of balticolid, a 12-membered macrolide is described.
The first stereoselective total synthesis of the Z-isomer of (6S,7R,9R)-6,7-dihydroxy-9-propylnon... more The first stereoselective total synthesis of the Z-isomer of (6S,7R,9R)-6,7-dihydroxy-9-propylnon-4-eno-9lactone involving Sharpless titanium(IV) mediated regioselective ring-opening reaction, Steglich esterification and RCM as the key steps is reported.
Tetrahedron Letters, 2013
Tetrahedron Letters, 2013
Tetrahedron Letters, 2012
European Journal of Organic Chemistry, Nov 30, 2023
RSC Adv., 2015
Triazine-aryl-bis-indole derivative inhibits phosphodiesterase activity.
RSC Advances, 2013
The first stereoselective total synthesis of the Z-isomer of (6S,7R,9R)-6,7-dihydroxy-9-propylnon... more The first stereoselective total synthesis of the Z-isomer of (6S,7R,9R)-6,7-dihydroxy-9-propylnon-4-eno-9lactone involving Sharpless titanium(IV) mediated regioselective ring-opening reaction, Steglich esterification and RCM as the key steps is reported.
Herein we report the first stereoselective total synthesis of phomonol via Sharpless asymmetric d... more Herein we report the first stereoselective total synthesis of phomonol via Sharpless asymmetric dihydroxylation and 6-exo-trig oxa-Michael addition as the key steps.
Herein the first total synthesis of balticolid, a 12-membered macrolide is described.
The first stereoselective total synthesis of the Z-isomer of (6S,7R,9R)-6,7-dihydroxy-9-propylnon... more The first stereoselective total synthesis of the Z-isomer of (6S,7R,9R)-6,7-dihydroxy-9-propylnon-4-eno-9lactone involving Sharpless titanium(IV) mediated regioselective ring-opening reaction, Steglich esterification and RCM as the key steps is reported.