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D L Boger

Showing results (31-40 of 85) with videos related to

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The Journal of Organic Chemistry|May 18, 2000
Two comparisons of the performance of positional scanning and deletion synthesis for the identification of active constituents in mixture combinatorial librariesD L Boger, J K Lee, J Goldberg, et al.
Bioorganic & Medicinal Chemistry|June 1, 1995
CC-1065 CBI analogs: an example of enhancement of DNA alkylation efficiency through introduction of stabilizing electrostatic interactionsD L Boger, W Yun, N Han, et al.
Bioorganic & Medicinal Chemistry|December 1, 1995
Key analogs of the tetrapeptide subunit of RA-VII and deoxybouvardinD L Boger, J Zhou, B Winter, et al.
The Journal of Organic Chemistry|October 29, 2000
Asymmetric synthesis of orthogonally protected L-threo-beta-hydroxyasparagineD L Boger, R J Lee, P Y Bounaud, et al.
Bioorganic & Medicinal Chemistry|February 1, 1994
Molecular basis for sequence selective DNA alkylation by (+)- and ent-(-)-CC-1065 and related agents: alkylation site models that accommodate the offset AT-rich adenine N3 alkylation selectivityD L Boger, D S Johnson, W Yun, et al.
Bioorganic & Medicinal Chemistry|February 1, 1994
Design, synthesis and evaluation of bouvardin, deoxybouvardin and RA-I-XIV pharmacophore analogsD L Boger, M A Patane, Q Jin, et al.
Bioorganic & Medicinal Chemistry|March 21, 1998
Synthesis of key sandramycin analogs: systematic examination of the intercalation chromophoreD L Boger, J H Chen, K W Saionz, et al.
Bioorganic & Medicinal Chemistry Letters|January 5, 1999
Higher order iminodiacetic acid libraries for probing protein-protein interactionsD L Boger, P Ducray, W Chai, et al.
The Journal of Organic Chemistry|October 2, 2001
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 domainD L Boger, H W Schmitt, B E Fink, et al.
Bioorganic & Medicinal Chemistry Letters|January 1, 1999
An endogenous sleep-inducing compound is a novel competitive inhibitor of fatty acid amide hydrolaseM P Patricelli, J E Patterson, D L Boger, et al.
Pageof 9

Showing results (31-40 of 85) with videos related to

Sort By:
Pageof 9
The Journal of Organic Chemistry|May 18, 2000
Two comparisons of the performance of positional scanning and deletion synthesis for the identification of active constituents in mixture combinatorial librariesD L Boger, J K Lee, J Goldberg, et al.
Bioorganic & Medicinal Chemistry|June 1, 1995
CC-1065 CBI analogs: an example of enhancement of DNA alkylation efficiency through introduction of stabilizing electrostatic interactionsD L Boger, W Yun, N Han, et al.
Bioorganic & Medicinal Chemistry|December 1, 1995
Key analogs of the tetrapeptide subunit of RA-VII and deoxybouvardinD L Boger, J Zhou, B Winter, et al.
The Journal of Organic Chemistry|October 29, 2000
Asymmetric synthesis of orthogonally protected L-threo-beta-hydroxyasparagineD L Boger, R J Lee, P Y Bounaud, et al.
Bioorganic & Medicinal Chemistry|February 1, 1994
Molecular basis for sequence selective DNA alkylation by (+)- and ent-(-)-CC-1065 and related agents: alkylation site models that accommodate the offset AT-rich adenine N3 alkylation selectivityD L Boger, D S Johnson, W Yun, et al.
Bioorganic & Medicinal Chemistry|February 1, 1994
Design, synthesis and evaluation of bouvardin, deoxybouvardin and RA-I-XIV pharmacophore analogsD L Boger, M A Patane, Q Jin, et al.
Bioorganic & Medicinal Chemistry|March 21, 1998
Synthesis of key sandramycin analogs: systematic examination of the intercalation chromophoreD L Boger, J H Chen, K W Saionz, et al.
Bioorganic & Medicinal Chemistry Letters|January 5, 1999
Higher order iminodiacetic acid libraries for probing protein-protein interactionsD L Boger, P Ducray, W Chai, et al.
The Journal of Organic Chemistry|October 2, 2001
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 domainD L Boger, H W Schmitt, B E Fink, et al.
Bioorganic & Medicinal Chemistry Letters|January 1, 1999
An endogenous sleep-inducing compound is a novel competitive inhibitor of fatty acid amide hydrolaseM P Patricelli, J E Patterson, D L Boger, et al.
Pageof 9