17 results on '"Batalla, Consuelo"'
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2. Synthesis of C3-substituted enantiopure 2-(p-tolylsulfinyl)-furans: the sulfoxide group as a chiral inductor for furan dienes as precursors of a wide variety of chiral intermediates
3. [4+3] Cycloaddition of C-3 substituted furans. Stereoselectivity induced by coordination effects
4. Unprecedented double benzylic rearrangement: regio- and stereospecific tandem 1,4-shift and Curtin rearrangement
5. Synthesis, characterization and antiproliferative studies of the enantiomers of cis-[(1,2-camphordiamine)dichloro]platinum(II) complexes
6. ChemInform Abstract: Use of the p-Tolylsulfinyl Group as a Chiral Inductor in Stereoselective [4 + 3] Cycloaddition Reactions: Preparation of Enantiopure Polysubstituted 8-Oxabicyclo[3.2.1]oct-6-en-3-one Systems Having up to Five Stereocenters.
7. ChemInform Abstract: Synthesis of C3‐Substituted Enantiopure 2‐(p‐Tolylsulfinyl)‐furans: The Sulfoxide Group as a Chiral Inductor for Furan Dienes as Precursors of a Wide Variety of Chiral Intermediates.
8. Use of thep-Tolylsulfinyl Group as a Chiral Inductor in Stereoselective [4+3] Cycloaddition Reactions: Preparation of Enantiopure Polysubstituted 8-Oxabicyclo[3.2.1]oct-6-en-3-one Systems Having up to Five Stereocenters
9. ChemInform Abstract: C2-Functionalized Furans as Dienes in [4 + 3] Cycloaddition Reactions
10. ChemInform Abstract: Intramolecular Haloetherification and Transannular Hydroxycyclization of Alkenes - A Synthetic Methodology to Obtain Polycyclic Ethers and Amines
11. Intramolecular Haloetherification and Transannular Hydroxycyclization of Alkenes. A Synthetic Methodology to Obtain Polycyclic Ethers and Amines
12. The Rational Design of Anticancer Platinum Complexes: The Importance of the Structure-Activity Relationship
13. C1?C2 Cleavage of C1-Functionalized 8-Oxabicyclo-[3.2.1]-oct-6-en-3-one. Stereoselective Preparation of 4-Substituted Butenolides.
14. Use of the p-Tolylsulfinyl Group as a Chiral Inductor in Stereoselective [4+3] Cycloaddition Reactions: Preparation of Enantiopure Polysubstituted 8-Oxabicyclo[3.2.1]oct-6-en-3-one Systems Having up to Five Stereocenters.
15. C1–C2 cleavage of C1-functionalized 8-oxabicyclo-[3.2.1]-oct-6-en-3-one. Stereoselective preparation of 4-substituted butenolides
16. ChemInform Abstract: C.
17. C1-C2 Cleavage of C1-Functionalized 8-Oxabicyclo-[3.2.1]-oct-6-en-3-one. Stereoselective Preparation of 4-Substituted Butenolides.
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