161 results on '"de la Moya Cerero, Santiago"'
Search Results
2. Water-trapping of unstable carbocations taking place into the inverted region of the Marcus equation. First experimental and computational evidence
3. The role of conformational flexibility on the catalytic activity of norbornane-derived β-, γ- and δ-amino alcohols
4. Evidence for different types of water participation in the solvolysis of 1-aamantyl, tert-butyl, and methyl chlorides from density functional theory computations
5. Understanding the catalytic role of flexible chiral δ-amino alcohols: the 1-(2-aminoethyl)norbornan-2-ol model
6. Enantiospecific access to 10- N-substituted camphors
7. Intramolecular-activation evidence for the unexpected Beckmann fragmentation of C(1)-substituted-7-bromonorbornane-2-ones
8. A novel enantiospecific route to 10-hydroxyfenchone: a convenient intermediate for C(10)- O-substituted fenchones
9. Solvent and stereoelectronic effects on the solvolysis rates of oxaspirocyclopropanated 1-norbornyl triflates and related bridgehead derivatives
10. About the Existence of Organic Oxonium Ions as Mechanistic Intermediates in Water Solution
11. Polyoxygenated ketopinic-acid-derived γ-amino alcohols in the enantioselective diethylzinc addition to benzaldehyde
12. The Mechanism of Hydrolysis of Aryldiazonium Ions Revisited: Marcus Theory vs. Canonical Variational Transition State Theory
13. Hydroxyamides versus amino alcohols in the enantioselective addition of diethylzinc to benzaldehyde
14. Hydroxyamide-catalyzed enantioselective addition of diethylzinc to benzaldehyde in the absence of titanium
15. N/N/O versus N/O/O and N/O amino isoborneols in the enantioselective ethylation of benzaldehyde
16. Cheap and Long-Life Reusable Polymer for Asymmetric Organozinc Catalysis Based on Camphor-Derived Hydroxyamides
17. Unexpected efficiency of non‐C2‐symmetric bis(hydroxyamide)‐based zinc‐chelate catalysts
18. Different influence of polyoxygenation on the catalytic activity of amido vs. amino isoborneols
19. ChemInform Abstract: Ketopinic Acid Derived Bis(hydroxy amides) as Cheap, Chiral Ligands for the Enantioselective Ethylation of Aromatic Aldehydes.
20. Ketopinic Acid Derived Bis(hydroxy amides) as Cheap, Chiral Ligands for the Enantioselective Ethylation of Aromatic Aldehydes
21. Unexpected reactivity of 1-amine-2-methylenenorbornane hydrochlorides with m-CPBA
22. Surprising obtention of an enantiopure eight-membered cyclic ether from camphor
23. Solvent and Stereoelectronic Effects on the Solvolysis Rates of Oxaspirocyclopropanated 1-Norbornyl Triflates and Related Bridgehead Derivatives
24. Erratum to “Hydroxyamide-catalyzed enantioselective addition of diethylzinc to benzaldehyde in the absence of titanium”
25. First Efficient Synthesis of Enantiopure Homoketopinic Acid.
26. First Efficient Synthesis of Enantiopure Homoketopinic Acid
27. Evidence for Different Types of Water Participation in the Solvolysis of 1-Adamantyl, tert-Butyl, and Methyl Chlorides from Density Functional Theory Computations
28. A new type of anomalous ozonolysis in strained allylic bicycloalkan-1-ols
29. Palladium(II)-catalyzed ring expansion of a 1-alkenyl cyclopentanol
30. Electron ionization mass spectral studies of bridgehead 7,7-dimethylnorbornane-based β -amino alcohols
31. Enantiospecific Access to Various C(9),C(10)‐Disubstituted Camphors: Scope and Limitations.
32. Enantiospecific Preparation of 10-(pyperidin-1-yl)Camphor: A Model Procedure for 10-Aminocamphors
33. Enantiospecific Access to Various C(9),C(10)-Disubstituted Camphors: Scope and Limitations
34. 2-exo- versus 2-endo-Hydroxyl in δ-amino norbornan-2-ol-based catalysts: investigating the role of the C(2) configuration in the asymmetric induction
35. Synthesis and catalytic activity of 10-(aminomethyl)isoborneol-based catalysts: the role of the C(2)-group on the asymmetric induction
36. Synthesis of 7‐anti‐Bromo‐3,3‐dimethyl‐2‐oxonorbornane‐1‐carboxylic Acid: A New Chiral Source from the Chiral Pool.
37. C(10)-Substituted Camphors and Fenchones by Electrophilic Treatment of 2-Methylenenorbornan-1-ols: Enantiospecificity, Scope, and Limitations
38. Unexpected Hydrolysis of a C(7)-Oxo-Substituted 2-Oxonorborn-1-yl Triflate: Norbornane-Ring Expansion versus Norbornane-Ring Contraction
39. Synthesis of 7-anti-bromo-3,3-dimethyl-2-oxonorbornane-1-carboxylic acid: a new chiral source from the chiral pool
40. The role of the substitution pattern on the catalytic activity of chiral bridgehead norbornane-derived β-amino alcohols
41. Comprehensive Study of the Methyl Effect on the Solvolysis Rates of Bridgehead Derivatives
42. Unexpected Bromine-Assisted Beckmann Fragmentation of a C1-Electron-Acceptor Substituted 7-Bromonorbornan-2-one Upon Hydroxylamine Treatment
43. Straightforward synthesis of (1 S )-10-dimethylaminomethylcamphor: an enantiospecific model procedure to C10 C-substituted camphor-derived chiral sources
44. Bridgehead-norbornane-derived β-amino alcohol catalysts: structural factors influencing the chirality transfer
45. A new enantiospecific synthetic procedure to the taxoid-intermediate 10-methylenecamphor, and 10-methylenefenchone
46. ChemInform Abstract: Chemoselective Reaction of Spiro[oxirane‐2,2′‐norborn]‐1′‐yl Triflates with Nucleophiles: A New Case of HSAB‐Principle Dependence.
47. ChemInform Abstract: First Efficient Preparation of Enantiopure 10‐Bromofenchone: The Key Intermediate to C10‐Substituted Fenchone‐Derived Chiral Sources.
48. Chemoselective reaction of spiro[oxirane-2,2′-norborn]-1′-yl triflates with nucleophiles: a new case of HSAB-principle dependence
49. From natural camphor to (1 R ,2 S )-2-chloromethyl-3-oxocyclopentanecarboxylic acid: a stereocontrolled approach to enantiopure sarkomycin
50. First efficient preparation of enantiopure 10-bromofenchone: the key intermediate to C10-substituted fenchone-derived chiral sources
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.