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1. Process Development of a Tricyclic Diazepine-Based IDH1 Mutant Inhibitor

2. Synthesis of the Thapsigargins

4. Pd/C Catalyzed Dehalogenation of (Hetero)aryls Using Triethyl-silane as Hydrogen Donor.

8. Development of a Stereoselective Synthesis of (1R,4R)- and (1S,4S)-2-Oxa-5-azabicyclo[2.2.2]octane

10. Intramolecular cycloprotonation of unsaturated terminal epoxides and chlorohydrins

13. Highly Diastereoselective Synthesis of a HCV NS5B Nucleoside Polymerase Inhibitor

14. A mild and efficient one-pot synthesis of 2-aminated benzoxazoles and benzothiazoles

15. Practical Asymmetric Synthesis of a Calcitonin Gene-Related Peptide (CGRP) Receptor Antagonist Ubrogepant

19. Practical Asymmetric Synthesis of a Calcitonin Gene-Related Peptide (CGRP) Receptor Antagonist Ubrogepant

21. Enantioselective Synthesis of a Highly Substituted Tetrahydrofluorene Derivative as a Potent and Selective Estrogen Receptor Beta Agonist

23. Asymmetric Synthesis of cis-2,5-Disubstituted Pyrrolidine, the Core Scaffold of β3-AR Agonists

24. A Synthesis of a Spirocyclic Macrocyclic Protease Inhibitor for the Treatment of Hepatitis C.

39. Development of a Scaleable Synthesis of a Partial Nicotinic Acid Receptor Agonist

41. The Synthesis of Azadirachtin: A Potent Insect Antifeedant

42. Cover Picture: The Synthesis of Azadirachtin: A Potent Insect Antifeedant (Chem. Eur. J. 34/2008)

46. Cover Picture: Total Synthesis of Five Thapsigargins: Guaianolide Natural Products Exhibiting Sub‐Nanomolar SERCA Inhibition (Chem. Eur. J. 20/2007)

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