17 results on '"Campos, Joaquin"'
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2. Synthesis and reactivity of ( RS)-6-chloro-7- or 9-(1,2,3,5-tetrahydro-4,1-benzoxazepin-3-yl)-7 H- or 9 H-purines bearing a nitrobenzenesulfonyl group on the nitrogen atom
3. 6′-Chloro-7- or 9-(2,3-dihydro-5 H-4,1-benzoxathiepin-3-yl)-7 H- or 9 H-purines and their corresponding sulfones as a new family of cytotoxic drugs
4. Synthesis and anticancer activity studies of novel 1-(2,3-dihydro-5 H-1,4-benzodioxepin-3-yl)uracil and (6′-substituted)-7- or 9-(2,3-dihydro-5 H-1,4-benzodioxepin-3-yl)-7 H- or 9 H-purines
5. Adjuvant hyperthermic intraperitoneal chemotherapy in locally advanced colon cancer (HIPECT4): A randomized, phase 3 study
6. Synthesis of novel 1-(2,3-dihydro-5 H-4,1-benzoxathiepin-3-yl)-uracil and -thymine, and their corresponding S-oxidized derivatives
7. Substituent effects on the reaction mode between 2-hydroxybenzyl alcohol derivatives and MEM chloride: synthesis and mechanistic aspects of seven- and ten-membered benzo-fused O, O-acetals
8. Synthesis of tetrahydrobenzoxazepine acetals with electron-withdrawing groups on the nitrogen atom. Novel scaffolds endowed with anticancer activity against breast cancer cells
9. Medium benzene-fused oxacycles with the 5-fluorouracil moiety: synthesis, antiproliferative activities and apoptosis induction in breast cancer cells
10. Neighbouring-group participation as the key step in the reactivity of acyclic and cyclic salicyl-derived O, O-acetals with 5-fluorouracil. Antiproliferative activity, cell cycle dysregulation and apoptotic induction of new O, N-acetals against breast cancer cells
11. Quantitative structure–activity relationships for a series of symmetrical bisquaternary anticancer compounds
12. cis- and trans-1-[3-(Hydroxymethyl)-1,4-dioxepan-5-yl]pyrimidines: a new nucleoside prototype with a seven-membered moiety
13. Anticancer activity of (1,2,3,5-tetrahydro-4,1-benzoxazepine-3-yl)-pyrimidines and -purines against the MCF-7 cell line: Preliminary cDNA microarray studies
14. QSAR of 1,1′-(1,2-ethylenebisbenzyl)bis(4-substitutedpyridinium) dibromides as choline kinase inhibitors: a different approach for antiproliferative drug design
15. Corrigendum to “Synthesis and reactivity of ( RS)-6-chloro-7- or 9-(1,2,3,5-tetrahydro-4,1-benzoxazepin-3-yl)-7 H- or 9 H-purines bearing a nitrobenzenesulfonyl group on the nitrogen atom” : [Tetrahedron 63 (2007) 5274]
16. Synthesis of novel 5-fluorouracil derivatives with 1,4-oxaheteroepane moieties
17. Chemical modifications on the acyclic moiety of 3-(2-hydroxyethoxy)-1-alkoxypropyl nucleobases. 2. Differentiation and growth inhibition in rhabdomyosarcoma cells after exposure to a novel 5-fluorouracil acyclonucleoside
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