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Molecular Diversity|September 20, 2017
Exploring the anti-proliferative activity of Pelargonium sidoides DC with in silico target identification and network pharmacologyA S P Pereira, M J Bester, Z Apostolides
Molecular Diversity|August 12, 2015
General synthesis of 2,1-benzisoxazoles (anthranils) from nitroarenes and benzylic C-H acids in aprotic media promoted by combination of strong bases and silylating agentsMichał Wiȩcław, Mariusz Bobin, Andrzej Kwast, et al.
Molecular Diversity|June 10, 2016
Synthesis and biological evaluation of novel tamoxifen-1,2,4-triazole conjugatesM S R Murty, Mohana Rao Katiki, Jagadeesh Babu Nanubolu, et al.
Molecular Diversity|June 3, 2016
Microbial diversification of Diels-Alder cycloadducts by whole cells of Penicillium brasilianumZia Ud Din, Taicia P Fill, M Carolina Donatoni, et al.
Molecular Diversity|May 28, 2016
Uniqueness: skews bit occurrence frequencies in randomly generated fingerprint librariesNelson G Chen
Molecular Diversity|June 14, 2016
Facile and efficient approach for the synthesis of spirocyclopropylbarbiturates and 3-substituted-1,1,2,2-tetracyanocyclopropanes using N-halosulfonamidesRamin Ghorbani-Vaghei, Yaser Maghbooli, Azadeh Shahriari, et al.
Molecular Diversity|August 2, 2015
Synthesis and anticancer activity of novel fused pyrimidine hybrids of myrrhanone C, a bicyclic triterpene of Commiphora mukul gum resinUppuluri Venkata Mallavadhani, Madasu Chandrashekhar, Vadithe Lakshma Nayak, et al.
Molecular Diversity|July 10, 2014
A green four-component synthesis of zwitterionic alkyl/benzyl pyrazolyl barbiturates and their photophysical studiesManisha Bihani, Pranjal P Bora, Ghanashyam Bez, et al.
Molecular Diversity|August 20, 2014
Synthesis of benzimidazole[2.1-b][1,3]oxazine spirooxindoles via three-component reaction of N-benzylbenzimidazole, acetylenedicarboxylates, and N-alkylisatinsLi-Juan Zhang, Chao-Guo Yan
Molecular Diversity|August 27, 2014
An in silico protocol for identifying mTOR inhibitors from natural productsLei Chen, Ling Wang, Qiong Gu, et al.
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