Regioselectivity stereoselectivity and catalysis in intermolecular Pauson-Khand reactions: Teaching an old dog new tricks
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Solvent-controlled selectivity in the synthesis of five-membered carbocycles from carbene complexes
Dirwald, F. Z. Solvent-controlled selectivity in the synthesis of five-membered carbocycles from carbene complexes. Angew. Chem. Int. Ed. 2003, 42, 1332-1334
Dynamic thermodynamic resolution: Control of enantioselectivity through diastereomeric equilibration
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Strategies for heterocyclic construction via novel multicomponent reactions based on isocyanides and nucleophilic carbenes
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An efficient method for the synthesis of benzo[f]quino-line and benzo[a]phenanthridine derivatives catalyzed by iodine by a three-component reaction of arenecarbaldehyde naphthalen-2-amine and cyclic ketone
Wang, X. S.; Li, Q.; Yao, C. S.; Tu, S. J. An efficient method for the synthesis of benzo[f]quino-line and benzo[a]phenanthridine derivatives catalyzed by iodine by a three-component reaction of arenecarbaldehyde, naphthalen-2-amine, and cyclic ketone. Eur. J. Org. Chem. 2008, 3513-3518
A novel and facile synthesis of 2-(cyclohexylamino)-6,7-dihydro-3-aryl- 1H-indole-4(5H)-ones via a one-pot multi-component reaction
Heravi, M. M.; Baghernejad, B.; Oskooie, H. A.; Hekmatshoar, R. A novel and facile synthesis of 2-(cyclohexylamino)-6,7-dihydro-3-aryl-1H-indole-4(5H)- ones via a one-pot multi-component reaction. Tetrahedron Lett. 2008, 49, 6101-6103
Regioselective three-component synthesis of highly fluorescent, 1, 3,5-trisubstituted pyrazoles
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Synthesis of new 1H-1 2,4-triazolylcoumar-ins and their antitumor and anti-HIV activities
Al-Soud, Y. A.; Al-Masoudi, I. A.; Saeed, B.; Beifuss, U.; Al-Masoudi, N. A. Synthesis of new 1H-1,2,4-triazolylcoumar-ins and their antitumor and anti-HIV activities. Chem. Heterocycl. Comp. 2006, 42, 583-590
Amino acid derivarives part I: Syn thesis, antiviral, and antitumor evaluation of new a-amino acid esters bearing coumarin side chain
Al-Masoudi, N. A.; Al-Masoudi, I. A.; Ali, I. A. I.; Al-Soud, Y. A.; Saeed, B.; La Colla, P. Amino acid derivarives, part I: Synthesis, antiviral, and antitumor evaluation of new a-amino acid esters bearing coumarin side chain. Acta Pharm. 2006, 56, 175-188.
Syn thesis characterization, and antimicrobial activity of a series of substituted coumarin-3-carboxylato silver(I) complexes
Creaven, B. S.; Egan, D. A.; Kavanagh, K.; McCann, M.; Noble, A.; Thati, B.; Walsh, M. Synthesis, characterization, and antimicrobial activity of a series of substituted coumarin-3-carboxylato silver(I) complexes. Inorgan. Chim. Acta 2006, 359, 3976-3984.
Modified coumarins 17: Synthesis and anticoagulant activity of 3,4-cycloannelated coumarin D-glycopyranosides
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Biological activities, and quality control parameters of the crude extract and essential oil from Arracacia tolucensis var. multifida
Figueroa, M.; Rivero-Cruz, I.; Rivero-Cruz, B.; Bye, R.; Navarrete, A.; Mata, R. Constituents, biological activities, and quality control parameters of the crude extract and essential oil from Arracacia tolucensis var. multifida. J. Ethnopharm. 2007, 113, 125-131
In vivo antitumor, in vitro antibacterial activity, and alkylating properties of phosphorohydrazine derivatives of coumarin and chromone
Nawrot-Modranka, J.; Nawrot, E.; Graczyk, J. In vivo antitumor, in vitro antibacterial activity, and alkylating properties of phosphorohydrazine derivatives of coumarin and chromone. Eur. J. Med. Chem. 2006, 41, 1301-1309.
A novel and green method for the synthesis of indeno[2,1-c]pyridine derivatives in ionic liquid catalyzed by malononitrile
Wang, X. S.; Wu, J. R.; Li, Q.; Yao, C. S.; Tu, S. J. A novel and green method for the synthesis of indeno[2,1-c]pyridine derivatives in ionic liquid catalyzed by malononitrile. Synlett 2008, 1185-1188
An efficient and highly selective method for the synthesis of 3-arylbenzoquinoline derivatives catalyzed by iodine via three-component reactions
Wang, X. S.; Li, Q.; Wu, J. R.; Li, Y. L.; Yao, C. S.; Tu, S. J. An efficient and highly selective method for the synthesis of 3-arylbenzoquinoline derivatives catalyzed by iodine via three-component reactions. Synthesis 2008, 1902-1910
An unexpected ring-opening of 2-pyrone ring in the synthesis of 1-arylbenzo[f]quinoline-2-carboxmide derivatives in aqueous media catalyzed by TEBAC
Wang X. S.,Zhang M. M.,Li Q.,Yao C. S.,Tu S. J., An unexpected ring-opening of 2-pyrone ring in the synthesis of 1-arylbenzo[f]quinoline-2- carboxmide derivatives in aqueous media catalyzed by TEBAC. Synlett, 2007, 3141-3144.
An improved and benign synthesis of 9,10-diarylacridin-1,8-dione and indenoquinoline derivatives from 3-arylamino-5,5-dimethylcyclohex-2-enone, arylaldehyde, and 1,3-dicarbonyl compound in ionic liquid medium
Wang, X. S.; Zhang, M. M.; Jiang, H.; Shi, D. Q.; Tu, S. J.; Wei, X. Y.; Zong, Z. M. An improved and benign synthesis of 9,10-diarylacridin-1,8-dione and indenoquinoline derivatives from 3-arylamino-5,5-dimethylcyclohex-2-enone, arylaldehyde, and 1,3-dicarbonyl compound in ionic liquid medium. Synthesis 2006, 4187-4199.
Studies on 4-hydroxycou-marins, ii: The condensation of aldehydes with 4-hydroxycoumarins
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