42 results on '"Calaza, M. Isabel"'
Search Results
2. A straightforward route to enantiopure α-substituted derivatives of (2S,3aS,7aS)-octahydroindole-2-carboxylic acid
3. NCAD, a database integrating the intrinsic conformational preferences of non-coded amino qcids
4. In silico molecular engineering for a targeted replacement in a tumor-homing peptide
5. Effect of a β-phenyl substituent on the puckering modes of proline
6. Integrating the intrinsic conformational preferences of non-coded α-amino acids modified at the peptide bond into the NCAD database
7. Integrating the intrinsic conformational preferences of noncoded alpha-amino acids modified at the peptide bond into the noncoded amino acids database
8. Synthesis of α-aminoboronic acids.
9. Towards the stereoselective synthesis of α-methylated (2 S,3a S,7a S)-octahydroindole-2-carboxylic acid
10. Synthesis of enantiomerically pure δ-benzylproline derivatives.
11. Synthesis of [ c]-Fused Bicyclic Proline Analogues.
12. Synthesis of Racemic δ,δ-Dimethylproline Derivatives.
13. Access to Enantiomerically Pure cis- and trans-β-Phenylproline by High-Performance Liquid Chromatography Resolution.
14. Practical access to the proline analogs ( S, S, S)- and ( R, R, R)-2-methyloctahydroindole-2-carboxylic acids by HPLC enantioseparation.
15. Access to the cis-Fused Stereoisomers of Proline Analogues Containing an Octahydroindole Core.
16. Synthesis and reaction of secondary and primary diorganozinc reagents using a boron–zinc exchange reaction: A useful method for the stereo- and regioselective formation of new carbon&z.sbnd;carbon bonds
17. Enantiospecific synthesis of N-(9-phenylfluoren-9-yl)-...-amino ketones.
18. ChemInform Abstract: Synthesis of α-Aminoboronic Acids.
19. ChemInform Abstract: Synthesis of [c]-Fused Bicyclic Proline Analogues.
20. ChemInform Abstract: Heterocycles from Amino Acids.
21. ChemInform Abstract: Access to the cis-Fused Stereoisomers of Proline Analogues Containing an Octahydroindole Core.
22. ChemInform Abstract: Stereoselective Synthesis of Quaternary Proline Analogues.
23. Carbon-Carbon Bond-Forming Reactions Mediated by Organozinc Reagents.
24. Stanna-Brook Rearrangement of Carboxylic Acid Derivatives. Synthetic Utility and Mechanistic Studies.
25. Stereoselective SN2-Substitutions Using Polyfunctional Lithium Arylcuprates Prepared by an Iodine-Copper Exchange.
26. Synthesis and Reaction of Secondary and Primary Diorganozinc Reagents Using a Boron-Zinc Exchange Reaction. A Useful Method for the Stereo- and Regioselective Formation of New Carbon-Carbon Bonds.
27. Highly Stereoselective anti SN2′ Substitutions of (Z)-Allylic Pentafluorobenzoates with Polyfunctionalized Zinc-Copper Reagents.
28. Highly anti-Selective SN2′ Substitutions of Chiral Cyclic 2-Iodo-allylic Alcohol Derivatives with Mixed Zinc-Copper Reagents.
29. One-Pot Chemoselective Functionalization of Arylsilanes via Cascade Metal-Metal Exchange Reactions.
30. ChemInform Abstract: Diastereoselective Synthesis and Reactions of Diorganozinc Reagents Obtained After Hydroborations with 9-BBN-H, Thexylborane and Catecholborane.
31. ChemInform Abstract: Application of Baldwin′s Rules for the Preparation of Stable, β-Leaving Group-Bearing Organolithium Compounds.
32. ChemInform Abstract: Conformationally Constrained Nicotines. 1-Pyridinyl-7-azabicyclo[2.2.1]heptane and 1-Pyridinyl-8-azabicyclo[3.2.1]octane Analogues.
33. β-Phenylproline: the high β-turn forming propensity of proline combined with an aromatic side chain.
34. Practical access to the proline analogs (S,S,S)- and (R,R,R)-2-methyloctahydroindole-2-carboxylic acids by HPLC enantioseparation.
35. NCAD, a database integrating the intrinsic conformational preferences of non-coded amino acids.
36. Stereoselective Synthesis of Quaternary Proline Analogues.
37. Versatile methodology for the synthesis and α-functionalization of (2R,3aS,7aS)-octahydroindole-2-carboxylic acid.
38. Stanna-Brook rearrangement of carboxylic acid derivatives. Synthetic utility and mechanistic studies.
39. Stereoselective S N 2-substitutions using polyfunctional lithium arylcuprates prepared by an iodine-copper exchange.
40. Substrate-controlled highly diastereoselective synthesis of primary and secondary diorganozinc reagents by hydroboration/boron-zinc exchange sequence.
41. Highly stereoselective anti SN2' substitutions of (Z)-allylic pentafluorobenzoates with polyfunctionalized zinc-copper reagents.
42. Highly anti-selective SN2' substitutions of chiral cyclic 2-iodo-allylic alcohol derivatives with mixed zinc-copper reagents.
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.