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750Kokel et al..
The non-genotoxic carcinogens naphthalene and para-dichlorobenzene suppress apoptosis in C, Nature Chemical Biology, 2006 S. Claessens, P. Habonimana and N. De Kimpe.
Synthesis of naturally occurring naphthoquinone epoxides and application in the synthesis of β-lapachone, Org. Biomol. Chem., 2010 Padmakar A. Suryavanshi, Vellaisamy Sridharan and J. Carlos Menéndez.
Expedient, one-pot preparation of fused indoles via CAN-catalyzed three-component domino sequences and their transformation into polyheterocyclic compounds containing pyrrolo[1,2-a]azepine, Org. Biomol. Chem., 2010, 8, 3426. Yun Liu, Hua-You Hu, Yan Zhang, Hong-Wen Hu and Jian-Hua Xu.
Synthesis of 1,2-annulated and 1,2-unsubstituted pyrrolo[2,1,5-de]quinolizin-5-ones (cycl[3.3.2]azin-5-ones) via [3+2] cycloadditions of 1-oxoquinolizinium ylides with cyclic alkenes, Org. Biomol. Chem., 2010, 8, 4921. Mariko Miyachi, Yoshinori Yamanoi, Yusuke Shibata, Hirokazu Matsumoto, Kazuo Nakazato, Masae Konno, Kohsuke Ito, Yasunori Inoue and Hiroshi Nishihara.
A photosensing system composed of photosystem I, molecular wire, gold nanoparticle, and double surfactants in water, Chem. Commun., 2010, 46, 2557. Dumitru Ghereg, Sakina Ech-Cherif El Kettani, Mohamed Lazraq, Henri Ranaivonjatovo, Wolfgang W. Schoeller, Jean Escudié and Heinz Gornitzka.
An isolable o-quinodimethane and its fixation of molecular oxygen to give an endoperoxide, Chem. Commun., 2009, 4821. José Carlos Netto-Ferreira, Virginie Lhiaubet-Vallet, Bauer Oliveira Bernardes, Aurelio Baird Buarque Ferreira and Miguel Ángel Miranda.
Characterization, reactivity and photosensitizing properties of the triplet excited state of α-lapachone, Phys. Chem. Chem. Phys., 2008, 10, 6645. Christophe Morin, Tatiana Besset, Jean-Claude Moutet, Martine Fayolle, Margit Brückner, Danièle Limosin, Katja Becker and Elisabeth Davioud-CharvetDelegate (E.D.C.) of Centre National de la Recherche Scientifique, France in the frame of a French–German cooperation with Heidelberg University, Germany..
The aza-analogues of 1,4-naphthoquinones are potent substrates and inhibitors of plasmodial thioredoxin and glutathione reductases and of human erythrocyteglutathione reductase, Org. Biomol. Chem., 2008, 6, 2731. José P. Da Silva, Edgar V. Bastos, Luis F. V. Ferreira and Richard G. Weiss.
Surface photochemistry of the herbicidenapropamide. The role of the media and environmental factors in directing the fates of intermediates, Photochem. Photobiol. Sci., 2008, 7, 69.