119 results on '"Tillyer, Richard D."'
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2. Stereoselective formation of carbon-carbon bonds via S(sub N)-displacement: Synthesis of substituted cycloalkyl[b]indoles
3. Stereoselective syntheses of highly functionalized bicyclo[3.1.0]hexanes: A general methodology for the synthesis of potent and selective mGluR2/3 agonists
4. Stereoselective conjugate addition reactions of alpha,beta-unsaturated tert-butyl esters with aryllithium reagents
5. The importance of synthetic chemistry in the pharmaceutical industry
6. Practical enantioselective synthesis of a COX-2 specific inhibitor
7. Correction to “A General Synthesis of Substituted Indoles from Cyclic Enol Ethers and Enol Lactones”
8. High pi-face selectivity in anti aldol reactions of E-enol borinates from chiral alkoxymethyl ketones: stereocontrolled synthesis of C24-C32 polyol subunit of rapamycin
9. Practical asymmetric synthesis of a potent PDE4 inhibitor via stereoselective enolate alkylation of a chiral aryl-heteroaryl secondary tosylate
10. Asymmetric synthesis of a prostaglandin D2 receptor antagonist
11. Highly efficient synthesis of Beta-amino acid derivatives via asymmetric hydrogenation of unprotected enamines
12. Highly diastereoselective heterogeneously catalyzed hydrogenation of enamines for the synthesis of chiral beta-amino acid derivatives
13. Rapid assembly of substituted dihydrocyclohepta(3,4)pyrrolo(1,2-alpha)indoles via a novel, carbene-based, rearrangement reaction
14. ChemInform Abstract: Rapid Assembly of Substituted Dihydrocyclohepta[3,4]pyrrolo[1,2-a]indoles via a Novel, Carbene-Based, Rearrangement Reaction.
15. ChemInform Abstract: Asymmetric Synthesis of an Endothelin Receptor Antagonist
16. Highly Regioselective Synthesis of 1-Aryl-3,4,5-Substituted Pyrazoles.
17. On the Mechanism of an Asymmetric α,β-Unsaturated Carboxylic Acid Hydrogenation: Application to the Synthesis of a PGD2 Receptor Antagonist
18. Stereoselective Formation of Carbon—Carbon Bonds via SN2-Displacement: Synthesis of Substituted Cycloalkyl[b]indoles.
19. (Z)-4-(Trimethylstannyl)-1,3-Butadienes : preparation and uses in organic synthesis
20. Stereoselective Formation of Carbon−Carbon Bonds via SN2-Displacement: Synthesis of Substituted Cycloalkyl[b]indoles
21. An efficient enzyme-catalyzed kinetic resolution: large-scale preparation of an enantiomerically pure indole-ethyl ester derivative, a key component for the synthesis of a prostaglandin D2 receptor antagonist, an anti-allergic rhinitis drug candidate
22. Practical Asymmetric Synthesis of a Potent PDE4 Inhibitor via Stereoselective Enolate Alkylation of a Chiral Aryl−Heteroaryl Secondary Tosylate
23. Highly Efficient Synthesis of β-Amino Acid Derivatives via Asymmetric Hydrogenation of Unprotected Enamines
24. Synthesis of Substituted Imidazoles via Organocatalysis.
25. Nucleophilic Displacement at Benzhydryl Centers: Asymmetric Synthesis of 1,1,Diarylalkyl Derivatives.
26. A General Synthesis of Substituted Indoles from Cyclic Enol Ethers and Enol Lactones.
27. Highly Diastereoselective Heterogeneously Catalyzed Hydrogenation of Enamines for the Synthesis of Chiral β-Amino Acid Derivatives
28. Nucleophilic Displacement at Benzhydryl Centers: Asymmetric Synthesis of 1,1-Diarylalkyl Derivatives
29. A General Synthesis of Substituted Indoles from Cyclic Enol Ethers and Enol Lactones
30. ChemInform Abstract: Practical Routes Toward the Synthesis of 2‐Halo‐ and 2‐Alkylamino‐4‐pyridinecarboxaldehydes.
31. Practical routes toward the synthesis of 2-halo- and 2-alkylamino-4-pyridinecarboxaldehydes
32. ChemInform Abstract: A Novel, Highly Enantioselective Ketone Alkynylation Reaction Mediated by Chiral Zinc Aminoalkoxides.
33. A Novel, Highly Enantioselective Ketone Alkynylation Reaction Mediated by Chiral Zinc Aminoalkoxides
34. Eine neue, hochenantioselektive Alkinylierung von Ketonen, die durch chirale Zinkaminoalkoxide gesteuert wird
35. Asymmetric Synthesis of an Endothelin Receptor Antagonist.
36. Practical Asymmetric Synthesis of Efavirenz (DMP 266), an HIV-1 Reverse Transcriptase Inhibitor
37. Enantioselective 1,4-addition of aryllithium reagents to α,β-unsaturated tert-butyl esters in the presence of chiral additives
38. Stereoselective Conjugate Addition Reactions of α,β-Unsaturated tert-Butyl Esters with Aryllithium Reagents
39. Pd(0)-catalyzed addition of Me3SnSnMe3 to α,β-alkynic aldehydes and ketones. Synthesis of (Z)-β-trimethylstannyl α,β-alkenic aldehydes and ketones. Preparation and synthetic uses of substituted (Z)-4-trimethylstannyl-1,3-butadienes
40. Enantioselective syntheses of bicyclo[3.1.0]hexane carboxylic acid derivatives by intramolecular cyclopropanation
41. Asymmetric reduction of keto oxime ethers using oxazaborolidine reagents. The enantioselective synthesis of cyclic amino alcohols
42. Studies in biomimetic polyether synthesis: Construction of an ABCD-ring subunit of etheromycin using polyepoxide cascade cyclisations.
43. 13-Asymmetric induction in the aldol reactions of α-methylene-β-alkoxy aldehydes
44. High π-face selectivity in anti aldol reactions of E-enol borinates from chiral alkoxymethyl ketones: stereocontrolled synthesis of a C24-C32 polyol subunit of rapamycin
45. Studies in biomimetic polyether synthesis: Synthesis of an A-ring subunit of etheromycin
46. Studies in polypropionate synthesis: high π-face selectivity in syn aldol reactions of tin(II) enolates from (R)- and (S)-1-benzyloxy-2-methylpentan-3-one.
47. Highly Regioselective Synthesis of 1-Aryl-3,4,5-Substituted Pyrazoles.
48. Stereoselective Formation of Carbon—Carbon Bonds via SN2-Displacement: Synthesis of Substituted Cycloalkyl[b]indoles.
49. Stereoselective Syntheses of Highly Functionalized Bicyclo[3.1.0]hexanes: A General Methodology for the Synthesis of Potent and Selective mGluR2/3 Agonists.
50. Asymmetric Synthesis of a Prostaglandin D2 Receptor Antagonist.
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