Search research articles
Contact Us
Filters
Showing results (1-10 of 20) with videos related to
Page
of 2
Sort By:
Tetrahedron Letters
|
April 4, 2007
Synthetic Studies Toward Bryostatin 1: Preparation of a C(1)-C(16) Fragment by Pyran Annulation
Gary E Keck, Dennie S Welch, Yam B Poudel
Journal of Medicinal Chemistry
|
October 18, 2024
Correction to "The New Frontier: Merging Molecular Glue Degrader and Antibody-Drug Conjugate Modalities To Overcome Strategic Challenges"
Yam B Poudel, Ruchita R Thakore, Eugene P Chekler
Journal of Medicinal Chemistry
|
September 4, 2024
The New Frontier: Merging Molecular Glue Degrader and Antibody-Drug Conjugate Modalities To Overcome Strategic Challenges
Yam B Poudel, Ruchita R Thakore, Eugene P Chekler
Journal of the American Chemical Society
|
January 10, 2013
A Pd(0)-mediated indole (macro)cyclization reaction
Steven P Breazzano, Yam B Poudel, Dale L Boger
Tetrahedron
|
August 15, 2015
Total synthesis of dihydrolysergic acid and dihydrolysergol: development of a divergent synthetic strategy applicable to rapid assembly of D-ring analogs
Kiyoun Lee, Yam B Poudel, Christopher M Glinkerman, et al.
Journal of the American Chemical Society
|
December 24, 2010
Total synthesis of bryostatin 1
Gary E Keck, Yam B Poudel, Thomas J Cummins, et al.
Bioorganic & Medicinal Chemistry Letters
|
May 15, 2012
Role of the C8 gem-dimethyl group of bryostatin 1 on its unique pattern of biological activity
Gary E Keck, Yam B Poudel, Arnab Rudra, et al.
Journal of the American Chemical Society
|
September 11, 2014
Synthesis of a des-B-ring bryostatin analogue leads to an unexpected ring expansion of the bryolactone core
Matthew B Kraft, Yam B Poudel, Noemi Kedei, et al.
Angewandte Chemie (International Ed. in English)
|
May 22, 2010
Molecular modeling, total synthesis, and biological evaluations of C9-deoxy bryostatin 1
Gary E Keck, Yam B Poudel, Arnab Rudra, et al.
Organic Letters
|
December 31, 2008
Substitution on the A-ring confers to bryopyran analogues the unique biological activity characteristic of bryostatins and distinct from that of the phorbol esters
Gary E Keck, Yam B Poudel, Dennie S Welch, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 20) with videos related to
Sort By:
Page
of 2
Tetrahedron Letters
|
April 4, 2007
Synthetic Studies Toward Bryostatin 1: Preparation of a C(1)-C(16) Fragment by Pyran Annulation
Gary E Keck, Dennie S Welch, Yam B Poudel
Journal of Medicinal Chemistry
|
October 18, 2024
Correction to "The New Frontier: Merging Molecular Glue Degrader and Antibody-Drug Conjugate Modalities To Overcome Strategic Challenges"
Yam B Poudel, Ruchita R Thakore, Eugene P Chekler
Journal of Medicinal Chemistry
|
September 4, 2024
The New Frontier: Merging Molecular Glue Degrader and Antibody-Drug Conjugate Modalities To Overcome Strategic Challenges
Yam B Poudel, Ruchita R Thakore, Eugene P Chekler
Journal of the American Chemical Society
|
January 10, 2013
A Pd(0)-mediated indole (macro)cyclization reaction
Steven P Breazzano, Yam B Poudel, Dale L Boger
Tetrahedron
|
August 15, 2015
Total synthesis of dihydrolysergic acid and dihydrolysergol: development of a divergent synthetic strategy applicable to rapid assembly of D-ring analogs
Kiyoun Lee, Yam B Poudel, Christopher M Glinkerman, et al.
Journal of the American Chemical Society
|
December 24, 2010
Total synthesis of bryostatin 1
Gary E Keck, Yam B Poudel, Thomas J Cummins, et al.
Bioorganic & Medicinal Chemistry Letters
|
May 15, 2012
Role of the C8 gem-dimethyl group of bryostatin 1 on its unique pattern of biological activity
Gary E Keck, Yam B Poudel, Arnab Rudra, et al.
Journal of the American Chemical Society
|
September 11, 2014
Synthesis of a des-B-ring bryostatin analogue leads to an unexpected ring expansion of the bryolactone core
Matthew B Kraft, Yam B Poudel, Noemi Kedei, et al.
Angewandte Chemie (International Ed. in English)
|
May 22, 2010
Molecular modeling, total synthesis, and biological evaluations of C9-deoxy bryostatin 1
Gary E Keck, Yam B Poudel, Arnab Rudra, et al.
Organic Letters
|
December 31, 2008
Substitution on the A-ring confers to bryopyran analogues the unique biological activity characteristic of bryostatins and distinct from that of the phorbol esters
Gary E Keck, Yam B Poudel, Dennie S Welch, et al.
Page
of 2