@article { ISI:000251275500002, title = {Expeditious assembly of 3,4-benzannulated 8-oxabicyclo[3.2.1]octane systems by [2+2+2] alkyne cyclotrimerisation: Total synthesis of (-)-bruguierol A}, journal = {European Journal of Organic Chemistry}, number = {33}, year = {2007}, month = {NOV}, pages = {5483-5486}, publisher = {WILEY-V C H VERLAG GMBH}, type = {Article}, address = {PO BOX 10 11 61, D-69451 WEINHEIM, GERMANY}, abstract = {

Facile construction of benzene-fused 8-oxabicyclo[3.2.1]octane systems by employing a cross alkyne cyclotrimerisation reaction was explored. With this procedure, (-)-bruguierol A was synthesised, and its absolute configuration was established.

}, keywords = {cyclotrimerisation, epoxidation, Total synthesis, Wilkinson{\textquoteright}s catalyst}, issn = {1434-193X}, doi = {10.1002/ejoc.200700648}, author = {Ramana, Chepuri V. and Salian, Sumanth R. and Gonnade, Rajesh G.} } @article { ISI:000306670200022, title = {InCl3-mediated addition of indole to isatogens: an expeditious synthesis of 13-deoxy-isatisine A}, journal = {Chemistry-A European Journal}, volume = {18}, number = {31}, year = {2012}, month = {JUL}, pages = {9601-9611}, publisher = {WILEY-V C H VERLAG GMBH}, address = {BOSCHSTRASSE 12, D-69469 WEINHEIM, GERMANY}, abstract = {

A strategy directed towards the total synthesis of isatisine A that involves several late-stage metal-catalyzed transformations that address the key carboncarbon and carbonheteroatom bond formations has been developed. As a part of this strategy, methods for the addition of indoles to isatogens that lead selectively to either 2,2-disubstituted N-hydroxyindolin-3-one or 2,2-disubstituted indolin-3-one compounds have been developed by employing InCl3 as a catalyst or as the reagent. The present methods provide the first examples of the additions of indoles to the isatogen nucleus. To demonstrate its viability, the synthesis of 13-deoxy-isatisine A has been completed in ten steps from a known and easily available lactone.

}, keywords = {indium, indoles, isatogens, Natural products, Total synthesis}, issn = {0947-6539}, doi = {10.1002/chem.201103604}, author = {Kumar, Chepuri V. Suneel and Puranik, Vedavati G. and Ramana, Chepuri V.} } @article { ISI:000336248900015, title = {Total synthesis of the putative structure of xylarinol B}, journal = {Chemistry-An Asian Journal}, volume = {9}, number = {6}, year = {2014}, month = {JUN}, pages = {1557-1562}, publisher = {WILEY-V C H VERLAG GMBH}, address = {BOSCHSTRASSE 12, D-69469 WEINHEIM, GERMANY}, abstract = {

The total synthesis of the putative structure of xylarinolB is described and the need to revise its structure is demonstrated. The central benzoxepine skeleton was constructed by employing a cobalt-mediated bimolecular [2+2+2] Reppe-Vollhardt alkyne cycloaddition reaction.

}, keywords = {Chiral pool, cobalt, Natural products, structure elucidation, Total synthesis}, issn = {1861-4728}, doi = {10.1002/asia.201301647}, author = {More, Atul A. and Ramana, Chepuri V.} } @article { ISI:000363080800011, title = {Formal total synthesis of (-)-kumausallene}, journal = {Tetrahedron}, volume = {71}, number = {45}, year = {2015}, month = {NOV}, pages = {8577-8584}, publisher = {PERGAMON-ELSEVIER SCIENCE LTD}, address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND}, abstract = {

Deacetylkumausyne-a penultimate intermediate in Tang{\textquoteright}s total synthesis of (-)-kumausallene has been synthesized employing a chiral pool approach and thus culminating in a formal total synthesis of kumausallene. The opening of an epoxide with alkyne (use of Birch reduction for the selective construction of E-pent-3-enyl group) and C-allylation have been used to introduce the pendant alkenyl side chains. Initial attempts to execute an alternative to Tang{\textquoteright}s route comprising a prior installation of the bromoallene unit via bromoetherification and subsequent S(N)2 displacement are unsuccessful. To overcome this, an alternative approach was developed to arrive at Deacetylkumausyne (another natural product that has been synthesized and characterized by Tang{\textquoteright}s group). Thus, this overall exercise has culminated in a formal total synthesis of (-)-kumausallene. (C) 2015 Elsevier Ltd. All rights reserved.

}, keywords = {Bis-THF natural products, Chiral pool, Deacetylkumausyne, Total synthesis, Wittig reaction}, issn = {0040-4020}, doi = {10.1016/j.tet.2015.09.027}, author = {Das, Shyamsundar and Ramana, Chepuri V.} } @article { ISI:000356549600021, title = {Total synthesis of (+)-petromyroxol}, journal = {Tetrahedron Letters}, volume = {56}, number = {25}, year = {2015}, month = {JUN}, pages = {3933-3935}, publisher = {PERGAMON-ELSEVIER SCIENCE LTD}, address = {THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, ENGLAND}, abstract = {

The total synthesis of (+)-petromyroxol establishing its absolute configuration has been accomplished. The strategy developed employs easily accessible carbohydrate building blocks and comprises flexible and scalable chemistry that allowed the synthesis of (+)-petromyroxol along with its three diastereomers varying the stereochemistry mainly at C5 and/or C6. (C) 2015 Elsevier Ltd. All rights reserved.

}, keywords = {Glucose diacetonide, Petromyroxol, Pheromone, Sea Lamprey, Total synthesis}, issn = {0040-4039}, doi = {10.1016/j.tetlet.2015.04.129}, author = {Mullapudi, Venkanna Babu and Ramana, Chepuri V.} } @article {48730, title = {Concise approach for the synthesis of the tetracyclic framework of Lycibarbarines A and B}, journal = {Tetrahedron Letters}, volume = {121}, year = {2023}, month = {MAY }, type = {Article}, abstract = {

A simple approach for the construction of the tetracyclic spiroketal skeleton of Lycibarbarine A and B has been described. Employing a solvent free condition for epoxide opening with tetrahydroquinoline as a key reaction to couple both the fragments, an oxidation followed by TBAF-mediated silyl deprotection spiroketalization establishes the complete tetracyclic core present in these natural products. (c) 2023 Elsevier Ltd. All rights reserved.

}, keywords = {Chiral pool approach, D -Glyceraldehyde, Tetracyclic spiroketal, Total synthesis}, issn = {0040-4039}, doi = {10.1016/j.tetlet.2023.154493}, author = {Shet, Manoj N. and Nechooli, Hemanth K. and Ramana, Chepuri V.} }