645 results on '"Boger, Dale L."'
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2. Computational Studies of Reactions of 1,2,4,5-Tetrazines with Enamines in MeOH and HFIP.
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3. Tetrachlorovancomycin: Total Synthesis of a Designed Glycopeptide Antibiotic of Reduced Synthetic Complexity.
4. Divergent Total Synthesis and Characterization of Maxamycins.
5. 1,2,3,5-Tetrazines: A General Synthesis, Cycloaddition Scope, and Fundamental Reactivity Patterns.
6. Acyclic and Heterocyclic Azadiene Diels–Alder Reactions Promoted by Perfluoroalcohol Solvent Hydrogen Bonding: Comprehensive Examination of Scope.
7. Next-Generation Diprovocims with Potent Human and Murine TLR1/TLR2 Agonist Activity That Activate the Innate and Adaptive Immune Response.
8. Alanine scan of [L-[Dap.sup.2]]ramoplanin A2 aglycon: Assessment of the importance of each residue
9. Total synthesis of piericidin A1 and B1 and key analogues
10. Total synthesis of (-)- and ent-()-vindoline and related alkaloids
11. Intramolecular Diels - Alder/1,3-dipolar cycloaddition cascade f 1,3,4-oxadiazoles
12. Diastereoselective Diels-Alder reactions of N-sulfonyl-1-aza-1,3-butadienes with optically active enol ethers: An asymmetric variant of the 1-azadiene Diels-Alder reaction
13. Elucidation of fatty acid amide hydrolase inhibition by potent alpha-ketoheterocycle derivatives from Monte Carlo simulations
14. DNA alkylation properties of yatakemycin
15. Total synthesis of the Ramoplanin A2 and Ramoplanose Aglycon
16. Mechanistic Insights into the Reaction of Amidines with 1,2,3-Triazines and 1,2,3,5-Tetrazines.
17. N1/N4 1,4-Cycloaddition of 1,2,4,5-Tetrazines with Enamines Promoted by the Lewis Acid ZnCl2.
18. Crystal structures of human GAR Tfase at low and high pH and with substrate beta-GAR
19. Total synthesis of anhydrolycorinone utilizing sequential intramolecular Diels-Alder reactions of a 1,3,4-oxadiazole
20. Mechanisms of in situ activation for DNA-targeting antitumor agents
21. Hairpin versus extended DNA binding of a substituted beta-alanine linked polyamide
22. Unexpected formation of an epoxide-derived multisubstrate adduct inhibitor on the active site of GAR transformylase
23. Parallel synthesis and evaluation of 132 (+)-1,2,9,9a-tetrahydrocyclopropa[c]benz[e]indol-4-one (CBI) analogues of CC-1065 and the duocarmycins defining the contribution of the DNA-binding domain
24. Metal cation complexation and activation of reversed CPyI analogues of CC-1065 and duocarmycin SA: partitioning the effects of binding and catalysis
25. Asymmetric total synthesis of ent(-)-roseophilin: assignment of absolute configuration
26. Synthesis and evaluation of a series of C3-substituted CBI analogues of CC-1065 and the duocarmycins
27. Total synthesis of Fostriecin (CI-920)
28. Synthesis, chemical properties, and biological evaluation of CC-1065 and duocarmycin analogues incorporating the 5-methoxycarbonyl-1,2,9,9a-tetrahydrocyclopropa[c]benz[e]indol-4-one alkylation subunits
29. Total synthesis of thiocoraline and BE-22179 and assessment of their DNA binding and biological properties
30. Total synthesis of the rubrolone aglycon
31. Thermal atropisomerism of teicoplanin aglycon derivatives: Preparation of the P,P,P and M,P,P atropisomers of the teicoplanin aglycon via selective equilibration of the DE ring system
32. Development of a solution-phase synthesis of minor groove binding bis-intercalators based on triostin A suitable for combinatorial synthesis
33. Synthesis and evaluation of 1,2,8,8a-tetrahydrocyclopropa[c]pyrrolo[3,2-e]indol-4(5H)-one, the parent alkylation subunit of CC-1065 and the duocarmycins: impact of the alkylation subunit substituents and its implications for DNA alkylation catalysis
34. Selective metal cation activation of a DNA alkylating agent: synthesis and evaluation of methyl 1,2,9,9a-tetrahydrocyclopropa[c]pyrido[3,2-e]indol-4-one-7-carboxylate (CPyI)
35. Total synthesis of ningalin B utilizing a heterocyclic azadiene Diels-Alder reaction and discovery of a new class of potent multidrug resistant (MDR) reversal agents
36. Two comparisons of the performance of positional scanning and deletion synthesis for the identification of active constituents in mixture combinatorial libraries
37. New insights into inhibitor design from the crystal structure and NMR studies of Escherichia coli GAR transformylase in complex with beta-GAR and 10-formyl-5,8,10-trideazafolic acid
38. Total synthesis and comparative evaluation of luzopeptin A-C and quinoxapeptin A-C
39. Total synthesis of the vancomycin aglycon
40. Convergent solution-phase combinatorial synthesis with multiplication of diversity through rigid biaryl and diarylacetylene couplings
41. Are the duocarmycin and CC-1065 DNA alkylation reactions acid-catalyzed? Solvolysis pH-rate profiles suggest they are not
42. Synthesis and evaluation of duocarmycin and CC-1065 analogues containing modifications in the subunit linking amide
43. Total synthesis of HUN-7293
44. Binding-induced activation of DNA alkylation by duocarmycin SA: insights from the structure of an indole derivative-DNA adduct
45. Solution phase combinatorial synthesis of biaryl libraries employing heterogeneous conditions for catalysis and isolation with size exclusion chromatography for purification
46. Total synthesis of phomazarin
47. Total syntheses of ningalin A, lamellarin O, lukianol A, and permethyl storniamide A utilizing heterocyclic azadiene Diels-Alder reactions
48. Critical role of the linking amide in CC-1065 and the duocarmycins: implications on the source of DNA alkylation catalysis
49. Synthesis and evaluation of a carbocyclic analogue of the CC-1065 and duocarmycin alkylation subunits: role of the vinylogous amide and implications on DNA alkylation catalysis
50. A systematic evaluation of the bleomycin A2 L-threonine side chain: its role in preorganization of a compact conformation implicated in sequence-selective DNA cleavage
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