@article {43217,
	title = {First synthesis of a noreremophilane isolated from the roots of ligularia przewalskii},
	journal = {Tetrahedron Letters},
	volume = {46},
	year = {2005},
	month = {AUG},
	pages = {5211-5213},
	abstract = {<p>The total synthesis of a natural product noreremophilane has been achieved in just three steps from readily available starting materials. A highly stereo- and regio-selective Diels-Alder reaction was the key step in Our synthesis. (c) 2005 Elsevier Ltd. All rights reserved.</p>},
	doi = {10.1016/j.tetlet.2005.05.130},
	author = {Reddy, D. Srinivasa and Palani, K. and Balasubrahmanyam, D. and Kamath, V. B. and Iqbal, Javed}
}
@article {43222,
	title = {Mild and efficient method for the synthesis of vinylogous carbamates from alkyl azides},
	journal = {Tetrahedron Letters},
	volume = {46},
	year = {2005},
	month = {FEB},
	pages = {979-982},
	abstract = {A mild and efficient one-pot method for the synthesis of vinylogous carbamates is reported starting from alkyl azides under a hydrogen atmosphere using 10\% Pd/C. The resulting products are useful intermediates for the synthesis of heterocyclic compounds, natural products, and in peptidomimetics. (C) 2004 Elsevier Ltd. All rights reserved.},
	doi = {10.1016/j.tetlet.2004.12.047},
	author = {Reddy, D. Srinivasa and Rajale, T. V. and Shivakumar, K. and Iqbal, Javed}
}
@article {43221,
	title = {Synthesis of small cyclic peptides constrained with 3-(3-aminomethylphenyl)propionic acid linkers using free radical-mediated macrocyclization},
	journal = {Tetrahedron Letters},
	volume = {46},
	year = {2005},
	month = {AUG},
	pages = {5207-5210},
	abstract = {In this letter, we report that small peptides (di- and tri-) having a 3-bromobenzyl group at the C-termini and an acryloyl group at the N-termini undergo an efficient Bu3SnH-AlBN mediated intramolecular free radical cyclization to afford cyclic peptides in good yields. We also propose that these cyclizations are occurring via a pre-organized acyclic structure dictated by a reverse turn (gamma/beta-turn). (c) 2005 Published by Elsevier Ltd.},
	doi = {10.1016/j.tetlet.2005.05.115},
	author = {Balraju, V. and Reddy, D. Srinivasa and Periasamy, M. and Iqbal, Javed}
}
@article {43212,
	title = {Concise asymmetric route to the antibiotic macrolides patulolide A and pyrenophorin},
	journal = {Tetrahedron Letters},
	volume = {47},
	year = {2006},
	month = {SEP},
	pages = {6623-6626},
	abstract = {In this letter, we describe an enantiospecific route to patulolide A and pyrenophorin through the synthesis of known protected seco acid precursors starting from commercially available (S)-ethyl lactate. (c) 2006 Elsevier Ltd. All rights reserved.},
	doi = {10.1016/j.tetlet.2006.07.026},
	author = {Rao, K. Srinivasa and Reddy, D. Srinivasa and Mukkanti, K. and Pal, Manojit and Iqbal, Javed}
}
@article {43213,
	title = {Synthesis of cyclic peptides using a palladium-catalyzed enyne cycloisomerization},
	journal = {Tetrahedron Letters},
	volume = {47},
	year = {2006},
	month = {MAY},
	pages = {3569-3571},
	abstract = {In this letter, we report a palladium-catalyzed enyne cycloisomerization of linear peptides to generate small cyclic peptides embedded with a conjugated 1,3-diene. The utility of these resulting macrocyclic dienes is demonstrated by carrying out [4+2] cycloadditions with dienophiles to generate constrained cyclic peptides with cyclic linkers. (c) 2006 Elsevier Ltd. All rights reserved.},
	doi = {10.1016/j.tetlet.2006.03.053},
	author = {Balraju, V. and Dev, R. Vasu and Reddy, D. Srinivasa and Iqbal, Javed}
}
@article {43210,
	title = {New route to eremophilanes: synthesis of (+/-)-eremophilenolide, (+/-)-eremophiledinone, and (+/-)-deoxyeremopetasidione},
	journal = {Tetrahedron Letters},
	volume = {49},
	year = {2008},
	month = {OCT},
	pages = {6084-6086},
	abstract = {A new and efficient route to the family of eremophilanes is reported. Key steps are the highly stereocontrolled Diels-Alder reaction and aldol condensation to furnish a cis-decalin system with the desired stereochemistry present in the eremophilane family of natural products. This approach is general and was utilized for the synthesis of (+/-)-eremophilenolide, (+/-)-eremophiledinone, and (+/-)-deoxyeremopetasidione. (C) 2008 Elsevier Ltd. All rights reserved.},
	doi = {10.1016/j.tetlet.2008.08.006},
	author = {Srinivas, P. and Reddy, D. Srinivasa and Kumar, K. Shiva and Dubey, P. K. and Iqbal, Javed and Das, Parthasarathi}
}
@article {43208,
	title = {Total synthesis of (+/-)-petasitolone and (+/-)-fukinone},
	journal = {Synthesis-Stuttgart},
	year = {2009},
	month = {NOV},
	pages = {3833-3837},
	abstract = {An efficient, general, and fully stereocontrolled synthesis of eremophilane-type compounds is disclosed. The approach features a highly diastereoselective Diels-Alder/aldol sequence to give a common intermediate, which is subsequently exploited to produce (+/-)-petasitolone and (+/-)-fukinone in a short sequence.},
	doi = {10.1055/s-0029-1218150},
	author = {Pasikanti, Srinivas and Reddy, D. Srinivasa and Iqbal, Javed and Dubey, Pramod Kumar and Das, Parthasarathi}
}
@article {43206,
	title = {Efficient synthesis of varenicline},
	journal = {Tetrahedron Letters},
	volume = {51},
	year = {2010},
	month = {JAN},
	pages = {151-152},
	abstract = {Synthesis of varenicline the antismoking drug has been achieved in six steps with 10\% overall yield. A Diels-Alder reaction, oxidative cleavage of an olefin and reductive amination remain as key steps in the synthesis (C) 2009 Elsevier Ltd. All rights reserved.},
	doi = {10.1016/j.tetlet.2009.10.107},
	author = {Pasikanti, Srinivas and Reddy, D. Srinivasa and Venkatesham, B. and Dubey, P. K. and Iqbal, Javed and Das, Parthasarathi}
}
@article {43203,
	title = {Novel pyrazole-3-carboxamide derivatives as cannabinoid-1 (CB1) antagonists: journey from non-polar to polar amides},
	journal = {Bioorganic \& Medicinal Chemistry Letters},
	volume = {21},
	year = {2011},
	month = {JAN},
	pages = {562-568},
	abstract = {The synthesis and biological evaluation of novel pyrazole-3-carboxamide derivatives as CB1 antagonists are described. As a part of eastern amide SAR, various chemically diverse motifs were introduced. In general, a range of modifications were well tolerated. Several molecules with high polar surface area were also indentified as potent CB1 receptor antagonists. The in vivo proof of principle for weight loss is exemplified with a lead compound from this series. (C) 2010 Elsevier Ltd. All rights reserved.},
	doi = {10.1016/j.bmcl.2010.10.055},
	author = {Sasmal, Pradip K. and Reddy, D. Srinivasa and Talwar, Rashmi and Venkatesham, B. and Balasubrahmanyam, D. and Kannan, M. and Srinivas, P. and Kumar, K. Shiva and Devi, B. Neelima and Jadhav, Vikram P. and Khan, Sanjoy K. and Mohan, Priya and Chaudhury, Hira and Bhuniya, Debnath and Iqbal, Javed and Chakrabarti, Ranjan}
}
@article { ISI:000325950600096,
	title = {Enantiodivergent routes to (+) and (-)-novioses from (-)-pantolactone},
	journal = {RSC Advances},
	volume = {3},
	number = {43},
	year = {2013},
	month = {AUG},
	pages = {20291-20297},
	publisher = {ROYAL SOC CHEMISTRY},
	address = {THOMAS GRAHAM HOUSE, SCIENCE PARK, MILTON RD, CAMBRIDGE CB4 0WF, CAMBS, ENGLAND},
	abstract = {<p>Noviose, a rare sugar moiety present in many biologically interesting molecules such as novobiocin and tiacumicin was obtained through formal synthesis in (+)- and (-)-forms starting from commercially available (-)-pantolactone in an enantiodivergent manner.</p>},
	issn = {2046-2069},
	doi = {10.1039/c3ra42891e},
	author = {Rajesh, B. M. and Shinde, Madhuri V. and Kannan, M. and Srinivas, Gujjary and Iqbal, Javed and Reddy, D. Srinivasa}
}
