L. M. MARTIN CABREJAS

Author

Also Known As

Cabrejas, L.M.M., L. M. M. Cabrejas, L. M. MARTIN CABREJAS, Luisa M Martín Cabrejas, Luisa M. Martin Cabrejas, Luisa M. Martín Cabrejas, Luisa M. Martin Cabrejas

Publications

709

Citations

H-Index

Concepts

All Affiliations

Universidad Autónoma de Madrid Eli Lilly (Spain)Eli Lilly (United States)Novartis (Switzerland)Albany Molecular Research (United States)

About

L. M. MARTIN CABREJAS is an author at Universidad Autónoma de Madrid specializing in organic chemistry, chemistry, and natural sciences.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Natural Sciences	8	8	503
2	Engineering	7	7	289
3	Biochemistry	6	6	384
4	Biomolecular Engineering	6	6	206
5	Medicine	4	4	279

L. M. MARTIN CABREJAS

Publications

693

Citations

H-Index

Page 1

	Year	Citations
Imidazolyl benzimidazoles and imidazo[4,5-b]pyridines as potent p38α MAP kinase inhibitors with excellent in vivo antiinflammatory properties Mary M. Mader, Alfonso de Dios, Chuan Shih, Bioorganic & Medicinal Chemistry Letters Molecular PharmacologyMedicinal ChemistryBiochemistryMedicineNatural Sciences	2007	114
Sanglifehrin−Cyclophilin Interaction: Degradation Work, Synthetic Macrocyclic Analogues, X-ray Crystal Structure, and Binding Data Richard Sedrani, Jörg Kallen, L. M. MARTIN CABREJAS, Journal of the American Chemical Society Molecular RecognitionMacrolide AnaloguesEngineeringBiochemistrySanglifehrin−cyclophilin Interaction	2003	110
Acyl Sulfonamide Anti-Proliferatives: Benzene Substituent Structure−Activity Relationships for a Novel Class of Antitumor Agents Karen L. Lobb, Philip A. Hipskind, James Aikins, Journal of Medicinal Chemistry Organic ChemistryChemistryHuman Tumor XenograftsRelated Diaryl AcylsulfonamidesPharmaceutical Chemistry	2004	67
Synthesis of Macrolide Analogues of Sanglifehrin by RCM: Unique Reactivity of a Ruthenium Carbene Complex Bearing an Imidazol-2-ylidene Ligand Jürgen Wagner, L. M. MARTIN CABREJAS, Catharine E. Grossmith, The Journal of Organic Chemistry Unique ReactivityMedicinal ChemistryMacrolide AnaloguesEngineeringImidazol-2-ylidene Ligand	2000	52
Design of Potent and Selective 2-Aminobenzimidazole-Based p38α MAP Kinase Inhibitors with Excellent in Vivo Efficacy Alfonso de Dios, Chuan Shih, Beatriz López de Uralde, Journal of Medicinal Chemistry Pharmaceutical ScienceDrug TargetCompound 18Vivo EfficacyPharmacotherapy	2005	51
Acyl sulfonamide anti-proliferatives. Part 2: Activity of heterocyclic sulfonamide derivatives Mary M. Mader, Chuan Shih, Eileen L. Considine, Bioorganic & Medicinal Chemistry Letters Medicinal ChemistryDerivative (Chemistry)Bioorganic ChemistryHeterocyclicBiochemistry	2004	49
Macrolide Analogues of the Novel Immunosuppressant Sanglifehrin: New Application of the Ring-Closing Metathesis Reaction L. M. MARTIN CABREJAS, Stefan Rohrbach, Dieter Wagner, Angewandte Chemie International Edition Combinatorial ChemistryMacrocyclic CoreOrganic ChemistryHeterocycle ChemistryChemical Biology	1999	47
Catalytic activity of chiral β-hydroxysulfoxides in the enantioselective addition of diethylzinc to benzaldehyde. M. Carmen Carreño, J.L.G. Ruano, M. Maestro, Tetrahedron Asymmetry EngineeringChiral β-HydroxysulfoxidesOrganic ChemistryCatalysisCatalytic Activity	1993	44
The sulfinyl group as a chiral inductor in asymmetric Diels-Alder reactions J. L. G. Ruano, Juan C. Carretero, M. Carmen Carreño, Pure and Applied Chemistry Organic ChemistrySulfinyl GroupStereoselective SynthesisChemistryAsymmetric Diels-alder Reactions	1996	27
Diels-Alder reaction of (S)-2-p-tolylsulfinyl-2-cyclopentenone with Dane's diene: an efficient approach to the enantioselective preparation of perhydro-cyclopenta[a]phenanthrenes Inés Alonso, Juan C. Carretero, J.L.G. Ruano, Tetrahedron Letters Natural Product SynthesisHeterocyclicEnantioselective PreparationAlkene MetathesisEfficient Approach	1994	26

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