132 results on '"Pardo, Domingo Gomez"'
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2. Syntheses of (S,S)-reboxetine via a catalytic stereospecific rearrangement of [beta]-amino alcohols
3. Highly enantioselective synthesis of [beta]-amino alcohols: a catalytic version
4. Enantioselective ring expansion of prolinol derivatives. Two formal syntheses of (−)-swainsonine
5. Reactivity of alpha-(benzoyloxy)crotylstannane with aldehydes in liquid phase and on solid support. Synthesis of substituted lactones
6. Radical cyclizations. A convergent total synthesis of (±)-γ-lycorane
7. Ring expansion of functionalized octahydroindoles to enantiopure cis-decahydroquinolines
8. Nickel-Catalyzed System for the Cross-Coupling of Alkenyl Methyl Ethers with Grignard Reagents under Mild Conditions.
9. ChemInform Abstract: TFA‐Promoted Direct C—H Sulfenylation at the C2 Position of Non‐Protected Indoles.
10. Synthesis of Substituted α-Trifluoromethyl Piperidinic Derivatives.
11. TFA-promoted direct C–H sulfenylation at the C2 position of non-protected indoles
12. Correction to Ring Expansion of Cyclic β-Amino Alcohols Induced by Diethylaminosulfur Trifluoride: Synthesis of Cyclic Amines with a Tertiary Fluoride at C3
13. First Intramolecular Alkylation of Nitriles with Primary and Secondary Alcohols Catalyzed by Iridium Complexes
14. Correction to Iridium-Catalyzed Hydrogen Transfer: Synthesis of Substituted Benzofurans, Benzothiophenes, and Indoles from Benzyl Alcohols
15. Correction to Monoalkylation of Acetonitrile by Primary Alcohols Catalyzed by Iridium Complexes
16. Synthesis of LY503430 by using a selective rearrangement of β-amino alcohols induced by DAST
17. Access to Optically Active 3-Aminopiperidines by Ring Expansion of Prolinols: Thermodynamic versus Kinetic Control
18. Enantioselective Synthesis of SSR 241586 by Using an Organo-Catalyzed Henry Reaction
19. ChemInform Abstract: Ring Expansion: Formal Total Synthesis of (-)-Paroxetine.
20. Ring enlargement and ring contraction induced by DAST
21. ChemInform Abstract: Rearrangement of β‐Amino Alcohols and Application to the Synthesis of Biologically Active Compounds
22. ChemInform Abstract: Daucus carota Mediated Reduction of Cyclic 3‐Oxo‐amines.
23. Rearrangement of β‐amino alcohols and application to the synthesis of biologically active compounds
24. Daucus carota Mediated-Reduction of Cyclic 3-Oxo-amines
25. ChemInform Abstract: Stereospecific Rearrangement of β‐Amino Alcohols Catalyzed by H2SO4.
26. Stereoselective Rearrangement of (Trifluoromethyl)prolinols to Enantioenriched 3-Substituted 2-(Trifluoromethyl)piperidines.
27. Enantioselective ring expansion of prolinols and ring-closing metathesis: formal synthesis of (-)-swainsonine
28. Enantioselective Ring Expansion via Aziridinium Intermediates: Synthesis of Substituted Piperidines from Substituted Pyrrolidines — Synthetic Applications
29. Palladium-Catalyzed Intermolecular α-Arylation of N-Protected 2-Piperidinones
30. Diastereoselective conjugate addition of organocuprates to chiral racemic olefinic amido esters. Formal total synthesis of paroxetine
31. A Formal Synthesis of (−)-Paroxetine by Enantioselective Ring Enlargement of a Trisubstituted Prolinol
32. Solid-Support Synthesis of 1,2-Diols and γ-Lactones Through Addition of α-(Benzoyloxy)crotylindium Reagents to Aldehydes
33. Reactivity of α-(Benzoyloxy)crotylstannane with Aldehydes in Liquid Phase and on Solid Support. Synthesis of Substituted Lactones
34. Ring Expansion: Synthesis of the Velbanamine Piperidine Core
35. Radical Cyclizations – Synthesis of γ-Lycorane
36. Ring Expansion – Formation of Optically Active 3-Hydroxypiperidines from Pyrrolidinemethanol Derivatives
37. Synthesis of spiro[quinoline-2,4′-piperidines] Heck versus radical reaction
38. A convenient route to spiropyrrolidinyl-oxindole alkaloids via C-3 substituted ene-pyrrolidine carbamate radical cyclization
39. Heck Reaction versus Free Radical Reaction for the Synthesis of Spiro[indoline-2,4′-piperidines]
40. A SHORT AND EFFICIENT SYNTHESIS OF ZAMIFENACIN A MUSCARINIC M3 RECEPTOR ANTAGONIST
41. An easy access to substituted aminopyranones from L-pyroglutamic acid
42. A Short Enantioselective Access to Pumiliotoxin 251D from L-Proline
43. Synthesis of 2-(Alkylamino)benzonitriles from α-(Bromoarylamino)nitriles
44. Formation of optically active 3-hydroxypiperidines
45. A very useful and mild method for the protection and deprotection of carboxylic acids
46. Ring Expansion of Cyclic β-Amino Alcohols Induced by Diethylaminosulfur Trifluoride: Synthesis of Cyclic Amines with a Tertiary Fluorine at C3.
47. Asymmetric Synthesis of an Antagonist of Neurokinin Receptors: SSR 241586.
48. Syntheses of (S,S)-Reboxetine via a Catalytic Stereospecific Rearrangement of β-Amino Alcohols.
49. Highly Enantioselective Synthesis of β-Amino Alcohols: A Catalytic Version.
50. Synthesis of Optically Active Substituted 3-Fluoropiperidines from Prolinols by Using DAST.
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