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4. Enhanced Ligand Discovery through Generative AI and Latent-Space Exploration: Application to the Mizoroki-Heck Reaction

5. Development of a Scalable Synthesis toward a KRAS G12C Inhibitor Building Block Bearing an All-Carbon Quaternary Stereocenter, Part 2: Asymmetric Synthesis via Shi Epoxidation

8. A Slug Flow Platform with Multiple Process Analytics Facilitates Flexible Reaction Optimization.

9. Feed-Forward Neural Network for Predicting Enantioselectivity of the Asymmetric Negishi Reaction

13. Process Development of the BACE Inhibitors BI 1147560 BS and BI 1181181 MZ

17. Discovery and Process Development of a Scalable Biocatalytic Kinetic Resolution toward Synthesis of a Sterically Hindered Chiral Ketone

18. Scalable copper‐catalyzed preparation of imidazopyridinones from iodopyridinyl ureas.

21. Carbamoyl Anion Addition to Azirines

22. Novel 1,4-homofragmentation via an [alpha]-lactone

23. A straightforward route to stereodefined functionalized cycloheptanols and cyclooctanols

24. Application of a Preformed Pd-BIDIME Precatalyst to Suzuki–Miyaura Cross-Coupling Reaction in Flow

25. Development of a Scalable, Chromatography-Free Synthesis of t-Bu-SMS-Phos and Application to the Synthesis of an Important Chiral CF3-Alcohol Derivative with High Enantioselectivity Using Rh-Catalyzed Asymmetric Hydrogenation

26. Remarkable [beta]-selectivity in the synthesis of [beta]-1-C-arylglucosides: stereoselective reduction of acetyl-protected methyl 1-C-arylglucosides without acetoxy-group participation

27. Preparation of the HIV Attachment Inhibitor BMS-663068. Part 4. Synthesis of the 6-Azaindole Core

28. Effective BI-DIME Ligand for Suzuki-Miyaura Cross-Coupling Reactions in Water with 500 ppm Palladium Loading and Triton X

29. Development of a concise, scalable synthesis of a CCR1 antagonist utilizing a continuous flow Curtius rearrangement

30. Sequential C–H Arylation and Enantioselective Hydrogenation Enables Ideal Asymmetric Entry to the Indenopiperidine Core of an 11β-HSD-1 Inhibitor

31. Kinetic evidence for a tetrameric transition state in the asymmetric autocatalytic alkylation of pyrimidyl aldehydes

35. Correction to “Commercial Synthesis of a Pyrrolotriazine-Fluoroindole Intermediate to Brivanib Alaninate: Process Development Directed toward Impurity Control”

37. Development of an Asymmetric Synthesis of a Chiral Quaternary FLAP Inhibitor

39. Rationalization of anomalous nonlinear effects in the alkylation of substituted benzaldehydes

40. Sequential C-H Arylation and Enantioselective Hydrogenation Enables Ideal Asymmetric Entry to the Indenopiperidine Core of an 11β-HSD-1 Inhibitor.

41. Synthesis of the 6-Azaindole Containing HIV-1 Attachment Inhibitor Pro-Drug, BMS-663068

42. Addressing the Configuration Stability of Lithiated Secondary Benzylic Carbamates for the Development of a Noncryogenic Stereospecific Boronate Rearrangement

43. Amine-Tunable Ruthenium Catalysts for Asymmetric Reduction of Ketones

47. A Practical Stereoselective Synthesis and Novel Cocrystallizations of an Amphiphatic SGLT-2 Inhibitor

48. Development of an Efficient Synthesis of Two CRF Antagonists for the Treatment of Neurological Disorders

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