<?xml version="1.0" encoding="UTF-8"?><xml><records><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Sutar, Revannath L.</style></author><author><style face="normal" font="default" size="100%">Kumar, Vinod</style></author><author><style face="normal" font="default" size="100%">Shingare, Rahul D.</style></author><author><style face="normal" font="default" size="100%">Thorat, Shridhar</style></author><author><style face="normal" font="default" size="100%">Gonnade, Rajesh G.</style></author><author><style face="normal" font="default" size="100%">Reddy, D. Srinivasa</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">General approach to N-heterocyclic carbenes with a fused tetracyclic core: ligands for suzuki-miyaura cross-coupling reaction</style></title><secondary-title><style face="normal" font="default" size="100%">European Journal of Organic Chemistry</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">C-C coupling</style></keyword><keyword><style  face="normal" font="default" size="100%">carbenes</style></keyword><keyword><style  face="normal" font="default" size="100%">Homogeneous catalysis</style></keyword><keyword><style  face="normal" font="default" size="100%">N ligands</style></keyword><keyword><style  face="normal" font="default" size="100%">synthetic methods</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2014</style></year><pub-dates><date><style  face="normal" font="default" size="100%">JUL</style></date></pub-dates></dates><number><style face="normal" font="default" size="100%">21</style></number><publisher><style face="normal" font="default" size="100%">WILEY-V C H VERLAG GMBH</style></publisher><pub-location><style face="normal" font="default" size="100%">BOSCHSTRASSE 12, D-69469 WEINHEIM, GERMANY</style></pub-location><pages><style face="normal" font="default" size="100%">4482-4486</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;The synthesis of an N-heterocyclic carbene (NHC) based on a tetracyclic scaffold by using simple, general, and scalable chemistry is disclosed. The developed route is suitable for introducing multiple substitutions on the tetracyclic scaffold. The utility of the present NHC as a ligand in the Suzuki-Miyaura cross-coupling reaction is demonstrated with a low catalyst loading.&lt;/p&gt;</style></abstract><issue><style face="normal" font="default" size="100%">21</style></issue><custom3><style face="normal" font="default" size="100%">Foreign</style></custom3><custom4><style face="normal" font="default" size="100%">3.13
</style></custom4></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ramesh, Remya</style></author><author><style face="normal" font="default" size="100%">Shingare, Rahul D.</style></author><author><style face="normal" font="default" size="100%">Kumar, Vinod</style></author><author><style face="normal" font="default" size="100%">Anand, Amitesh</style></author><author><style face="normal" font="default" size="100%">Swetha, B.</style></author><author><style face="normal" font="default" size="100%">Veeraraghavan, Sridhar</style></author><author><style face="normal" font="default" size="100%">Viswanadha, Srikant</style></author><author><style face="normal" font="default" size="100%">Ummanni, Ramesh</style></author><author><style face="normal" font="default" size="100%">Gokhale, Rajesh S.</style></author><author><style face="normal" font="default" size="100%">Reddy, D. Srinivasa</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Repurposing of a drug scaffold: identification of novel sila analogues of rimonabant as potent antitubercular agents</style></title><secondary-title><style face="normal" font="default" size="100%">European Journal of Medicinal Chemistry</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2016</style></year><pub-dates><date><style  face="normal" font="default" size="100%">OCT</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">122</style></volume><pages><style face="normal" font="default" size="100%">723-730</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;The structural similarity between an MmpL3 inhibitor BM212, and a cannabinoid receptor modulator rimonabant, prompted us to investigate the anti-tubercular activity of rimonabant and its analogues. Further optimization, particularly through incorporation of silicon into the scaffold, resulted in new compounds with significant improvement in anti-tubercular activity against Mycobacterium tuberculosis (H37Rv). The sila analogue 18a was found to be the most potent antimycobacterial compound (MIC, 31 ng/mL) from this series with an excellent selectivity index. (C) 2016 Elsevier Masson SAS. All rights reserved.&lt;/p&gt;</style></abstract><custom3><style face="normal" font="default" size="100%">&lt;p&gt;Foreign&lt;/p&gt;</style></custom3><custom4><style face="normal" font="default" size="100%">3.902</style></custom4></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Agarwalla, Ankit</style></author><author><style face="normal" font="default" size="100%">Kumar, Vinod</style></author><author><style face="normal" font="default" size="100%">Mohanty, Kaustubha</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Techno-economic analysis of an integrated membrane-based harvesting and effluent recycling strategy for microalgal biomass production in raceway ponds</style></title><secondary-title><style face="normal" font="default" size="100%">ACS ES&amp;T Water</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2025</style></year><pub-dates><date><style  face="normal" font="default" size="100%">SEP</style></date></pub-dates></dates><volume><style face="normal" font="default" size="100%">5</style></volume><pages><style face="normal" font="default" size="100%">6078–6089</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p&gt;
	&lt;span style=&quot;color: rgb(21, 21, 21); font-family: Roboto, arial, sans-serif; font-size: 16px;&quot;&gt;Microalgae-based systems offer a sustainable route for biomass production and carbon dioxide (CO&lt;/span&gt;&lt;span style=&quot;box-sizing: border-box; outline: none; line-height: 0; position: relative; vertical-align: baseline; bottom: -0.25em; color: rgb(21, 21, 21); font-family: Roboto, arial, sans-serif;&quot;&gt;2&lt;/span&gt;&lt;span style=&quot;color: rgb(21, 21, 21); font-family: Roboto, arial, sans-serif; font-size: 16px;&quot;&gt;) capture; however, their economic feasibility remains scale-dependent. This study presents a techno-economic analysis (TEA) of&amp;nbsp;&lt;/span&gt;&lt;i style=&quot;box-sizing: border-box; outline: none; color: rgb(21, 21, 21); font-family: Roboto, arial, sans-serif; font-size: 16px;&quot;&gt;Monoraphidium&lt;/i&gt;&lt;span style=&quot;color: rgb(21, 21, 21); font-family: Roboto, arial, sans-serif; font-size: 16px;&quot;&gt;&amp;nbsp;sp. KMC4 cultivated in open raceway ponds (ORPs) using low-cost kaolin-based ceramic membranes integrated with a three-batch effluent recycling system. Four scenarios (S1–S4) were evaluated to assess the influence of production scale (1–100 ha) and electricity subsidies. Capital expenditure (CAPEX) and operating expenditure (OPEX) were quantified, and a sensitivity analysis was conducted for plant life, discount rate, biomass selling price, and utility and labor costs. Results show that small-scale systems with subsidies (S1) yield marginal profitability (net present value, NPV: $0.28 million), while unsubsidized small-scale systems (S2) remain unviable. Industrial-scale production (S4) demonstrated favorable economics with a unit biomass cost of $7.50 per kilogram, a payback period of 5.3 years, and an NPV of $145.78 million. The sensitivity analysis confirmed that the biomass selling price and utility costs are the most influential parameters that affect economic viability. Overall, the findings emphasize that economies of scale, process optimization, and resource recovery are key to widespread adoption and the feasibility of algae-based systems.&lt;/span&gt;&lt;/p&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">10</style></issue><work-type><style face="normal" font="default" size="100%">Article</style></work-type><custom3><style face="normal" font="default" size="100%">&lt;p&gt;
	Foreign&lt;/p&gt;
</style></custom3><custom4><style face="normal" font="default" size="100%">&lt;p&gt;
	4.7&lt;/p&gt;
</style></custom4></record></records></xml>