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Application of the Atoms in Molecules Theory to Y-3 X and Y-3 XZ (Y = H or CH3; X = N, P or As; Z = O or S) compounds84618471, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=8981]], camposKey:0022-2860 1998-06-08 Empirical relationship between structure and molecular optical rotation in polyhydroxycyclohexanes127133, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=8982]], camposKey:0022-2860 1998-02-03 Empirical relationship between structure and molecular optical rotation in tetrahydropyran derivatives135143, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=8970]], camposKey:0022-2860 1996-01-01 Conformational comparative analysis of pyrimidine nucleoside derivatives by molecular mechanics calculations and by semiempirical methods (AM1)2533, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=8978]], camposKey:0022-2860 1995-07-01 EMPIRICAL RELATIONSHIP BETWEEN STRUCTURE AND MOLECULAR OPTICAL-ROTATION IN CYCLOHEXANE DERIVATIVES .2.8187, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=8977]], camposKey:0022-2860 1995-01-01 CONFORMATIONAL COMPARATIVE-ANALYSIS OF 2',3'-DIDEOXYTHYMIDINE ANALOGS BY MOLECULAR MECHANICS CALCULATIONS (CHEM-X) AND BY SEMIEMPIRICAL METHODS (AM1)147160, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=8971]], camposKey:0022-2860 1994-01-01 EMPIRICAL RELATIONSHIP BETWEEN STRUCTURE AND MOLECULAR OPTICAL-ROTATION IN CYCLOHEXANE DERIVATIVES239247, com.sigma.fs3.argos.domain.gpc.GpcArticlesRev[id=com.sigma.fs3.argos.domain.gpc.GpcArticlesRevPK[ifcactivitat=ARE, ifccomptador=52103]], camposKey:0211-1357 1994-01-01 SYNTHESIS OF 2-O-METHYL AND 2-O-ACETYL-3,4-O-ISOPROPYLIDENE-D-THREOSE AND D-ERITHROSE
DERIVATIVES.212216][CapitolsLlib{id=com.sigma.fs3.argos.domain.gpc.GpcCapitolsLlibPK[ifcactivitat=CAP, ifccomptador=2068]},camposKey: 337 353 N-O and P-O bond nature in hypervalent compounds: is Bader analysis basis-set and geometry independent? 978-0-7923-5970-8Quantum Systems in Chemistry and Physics. Volume 2: Advanced Problems and Complex Systems Granada 1 2000-01-01 Springer][][Llibres{id=com.sigma.fs3.argos.domain.gpc.GpcLlibresPK[ifcactivitat=LLI, ifccomptador=115423],camposKey=978-0-12-803893-2Experimental Organic Chemistry: Laboratory Manual 1 2015-01-01 Academic Press}, Llibres{id=com.sigma.fs3.argos.domain.gpc.GpcLlibresPK[ifcactivitat=LLI, ifccomptador=115432],camposKey=978-84-1545-257-7Tratado de Química Orgánica Experimental 1 2013-01-01 Garceta}][][][][][][][][][][][][][][][com.sigma.fs3.argos.domain.gpc.GpcComissioAssessor[id=com.sigma.fs3.argos.domain.gpc.GpcComissioAssessorPK[ifcactivitat=COM, ifccomptador=1272]]][GpcPartTribunals[ gpcPartTribunalsPK=GpcPartTribunalsPK[ ifcactivitat=PTR, ifccomptador=1061 ] ], GpcPartTribunals[ gpcPartTribunalsPK=GpcPartTribunalsPK[ ifcactivitat=PTR, ifccomptador=947 ] ], GpcPartTribunals[ gpcPartTribunalsPK=GpcPartTribunalsPK[ ifcactivitat=PTR, ifccomptador=634 ] ]][com.sigma.investigacion.cawdos.utilidades.CongresoYSusAsociaciones@2ba014eb, com.sigma.investigacion.cawdos.utilidades.CongresoYSusAsociaciones@60f5be51, com.sigma.investigacion.cawdos.utilidades.CongresoYSusAsociaciones@3b9ac052, com.sigma.investigacion.cawdos.utilidades.CongresoYSusAsociaciones@52bc005e, com.sigma.investigacion.cawdos.utilidades.CongresoYSusAsociaciones@799051ae, com.sigma.investigacion.cawdos.utilidades.CongresoYSusAsociaciones@34da7ffb, com.sigma.investigacion.cawdos.utilidades.CongresoYSusAsociaciones@592fa162, com.sigma.investigacion.cawdos.utilidades.CongresoYSusAsociaciones@6ba3f4e9, com.sigma.investigacion.cawdos.utilidades.CongresoYSusAsociaciones@10c5d512, com.sigma.investigacion.cawdos.utilidades.CongresoYSusAsociaciones@77874556, com.sigma.investigacion.cawdos.utilidades.CongresoYSusAsociaciones@5307ce75, com.sigma.investigacion.cawdos.utilidades.CongresoYSusAsociaciones@27f77c40, com.sigma.investigacion.cawdos.utilidades.CongresoYSusAsociaciones@192440e9, com.sigma.investigacion.cawdos.utilidades.CongresoYSusAsociaciones@54441b6e, com.sigma.investigacion.cawdos.utilidades.CongresoYSusAsociaciones@395d13f5, com.sigma.investigacion.cawdos.utilidades.CongresoYSusAsociaciones@25546de2, com.sigma.investigacion.cawdos.utilidades.CongresoYSusAsociaciones@1e4c52a9, com.sigma.investigacion.cawdos.utilidades.CongresoYSusAsociaciones@6a27b565, com.sigma.investigacion.cawdos.utilidades.CongresoYSusAsociaciones@3bb4c16f, com.sigma.investigacion.cawdos.utilidades.CongresoYSusAsociaciones@3d898086, com.sigma.investigacion.cawdos.utilidades.CongresoYSusAsociaciones@41ac4484, com.sigma.investigacion.cawdos.utilidades.CongresoYSusAsociaciones@16774d49, com.sigma.investigacion.cawdos.utilidades.CongresoYSusAsociaciones@b555951, com.sigma.investigacion.cawdos.utilidades.CongresoYSusAsociaciones@7aa9650d, com.sigma.investigacion.cawdos.utilidades.CongresoYSusAsociaciones@598286b8, com.sigma.investigacion.cawdos.utilidades.CongresoYSusAsociaciones@75b385c4][][][][][][][com.sigma.fs3.argos.domain.gpc.GpcExpGestionId[id=com.sigma.fs3.argos.domain.gpc.GpcExpGestionIdPK[ifcactivitat=EXP, ifccomptador=403]]][][][com.sigma.investigacion.cawdos.entities.ayudaInvestigacion.ProjectesPPC[id=com.sigma.fs3.argos.domain.gpc.ayudasrecerca.ProjectesPPCId@467bec], com.sigma.investigacion.cawdos.entities.ayudaInvestigacion.ProjectesPPC[id=com.sigma.fs3.argos.domain.gpc.ayudasrecerca.ProjectesPPCId@466ff7], com.sigma.investigacion.cawdos.entities.ayudaInvestigacion.ProjectesPPC[id=com.sigma.fs3.argos.domain.gpc.ayudasrecerca.ProjectesPPCId@414e59], com.sigma.investigacion.cawdos.entities.ayudaInvestigacion.ProjectesPPC[id=com.sigma.fs3.argos.domain.gpc.ayudasrecerca.ProjectesPPCId@45f92b], com.sigma.investigacion.cawdos.entities.ayudaInvestigacion.ProjectesPPC[id=com.sigma.fs3.argos.domain.gpc.ayudasrecerca.ProjectesPPCId@4133a2], com.sigma.investigacion.cawdos.entities.ayudaInvestigacion.ProjectesPPC[id=com.sigma.fs3.argos.domain.gpc.ayudasrecerca.ProjectesPPCId@4605a8], com.sigma.investigacion.cawdos.entities.ayudaInvestigacion.ProjectesPPC[id=com.sigma.fs3.argos.domain.gpc.ayudasrecerca.ProjectesPPCId@460452], com.sigma.investigacion.cawdos.entities.ayudaInvestigacion.ProjectesPPC[id=com.sigma.fs3.argos.domain.gpc.ayudasrecerca.ProjectesPPCId@460467], com.sigma.investigacion.cawdos.entities.ayudaInvestigacion.ProjectesPPC[id=com.sigma.fs3.argos.domain.gpc.ayudasrecerca.ProjectesPPCId@411d57], com.sigma.investigacion.cawdos.entities.ayudaInvestigacion.ProjectesPPC[id=com.sigma.fs3.argos.domain.gpc.ayudasrecerca.ProjectesPPCId@45f417]][][][][][IftpertinEntitats[ iftpertinEntitatsPK=IftpertinEntitatsPK[ ifcactivitat=PEC, ifccomptador=260 ] ]][com.sigma.fs3.argos.domain.gpc.altres.ProjecteInnovacio@17459, com.sigma.fs3.argos.domain.gpc.altres.ProjecteInnovacio@17436, com.sigma.fs3.argos.domain.gpc.altres.ProjecteInnovacio@13ce2, com.sigma.fs3.argos.domain.gpc.altres.ProjecteInnovacio@13ce1][]