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The Synthesis of CP-263,114 and CP-225,917: Striking Long-Range Stereocontrol in the Fashioning of C7 Financial support was provided by the National Institutes of Health (Grant nos. CA-28824 and HL-25848 for S.J.D., CA-08748 for the Sloan-Kettering Institute Core Facility). Q.T. gratefully acknowledges the US Department of Defense for a postdoctoral fellowship (U.S. Army grant no. DAMD-17-99-1-9373). We thank the Pfizer Corporation, particularly Dr. T. Kaneko and Dr. T. T. Dabrah for discussions and for providing valuable CP samples from fermentation broth. We are grateful to Dr. Dongfang Meng for his major contributions to this work. We also thank George Sukenick of the Sloan-Kettering Institute Core Facility for mass spectral analyses and assistance in NMR spectroscopic and HPLC analyses, and Sylvi Rusli for mass spectral analyses.
Tan Q, Danishefsky SJ. Tan Q, et al. Among authors: danishefsky sj. Angew Chem Int Ed Engl. 2000 Dec 15;39(24):4509-4511. Angew Chem Int Ed Engl. 2000. PMID: 11169652 No abstract available.
From Glycals to Glycopeptides: A Convergent and Stereoselective Total Synthesis of a High Mannose N-Linked Glycopeptide This work was supported by the National Institutes of Health (Grant Numbers AI16943/CA28824). We thank Dr. George Sukenick of the MSKCC NMR Core Facility for NMR and mass spectral analyses (NIH Grant Number: CA08748).
Wang ZG, Zhang X, Live D, Danishefsky SJ. Wang ZG, et al. Among authors: danishefsky sj. Angew Chem Int Ed Engl. 2001 Feb 16;40(4):647. Angew Chem Int Ed Engl. 2001. PMID: 11241590 No abstract available.
The Synthesis of CP-263,114 and CP-225,917: Striking Long-Range Stereocontrol in the Fashioning of C7 Financial support was provided by the National Institutes of Health (Grant nos. CA-28824 and HL-25848 for S.J.D., CA-08748 for the Sloan-Kettering Institute Core Facility). Q.T. gratefully acknowledges the US Department of Defense for a postdoctoral fellowship (U.S. Army grant no. DAMD-17-99-1-9373). We thank the Pfizer Corporation, particularly Dr. T. Kaneko and Dr. T. T. Dabrah for discussions and for providing valuable CP samples from fermentation broth. We are grateful to Dr. Dongfang Meng for his major contributions to this work. We also thank George Sukenick of the Sloan-Kettering Institute Core Facility for mass spectral analyses and assistance in NMR spectroscopic and HPLC analyses, and Sylvi Rusli for mass spectral analyses.
Tan Q, Danishefsky SJ. Tan Q, et al. Among authors: danishefsky sj. Angew Chem Int Ed Engl. 2001 Feb 16;40(4):647. doi: 10.1002/1521-3773(20010216)40:4<647::aid-anie6473>3.0.co;2-g. Angew Chem Int Ed Engl. 2001. PMID: 11241592 No abstract available.
Toward Fully Synthetic Homogeneous Glycoproteins: A High Mannose Core Containing Glycopeptide Carrying Full H-Type 2 Human Blood Group Specificity This work was supported by the National Institutes of Health (Grant nos.: HL-25848 and CA-28824 (to S.J.D.), and CA-710506 (to K.O.L.)). Postdoctoral fellowship support is gratefully acknowledged by Z.-G.W. (US Army breast cancer grant no.: DAMD17-97-1-7119) and M.V. (NIH grant no.: CA-62948-04). We gratefully acknowledge Dr. George Sukenick of the Sloan-Kettering Institute's NMR core facility for mass spectral and NMR spectroscopic analyses (SKI core grant no.: CA-08748).
Wang ZG, Zhang X, Visser M, Live D, Zatorski A, Iserloh U, Lloyd KO, Danishefsky SJ. Wang ZG, et al. Among authors: danishefsky sj. Angew Chem Int Ed Engl. 2001 May 4;40(9):1728-1732. Angew Chem Int Ed Engl. 2001. PMID: 11353493 No abstract available.
Synthesis of the Functionalized Macrocyclic Core of Proteasome Inhibitors TMC-95A and B This work was supported by grants from the National Institutes of Health (grant CA28824). We thank Dr. George Sukenick and Sylvi Rusli of the MSKCC NMR Core Facility for NMR and mass spectral analyses (NIH Grant CA08748).
Lin S, Danishefsky SJ. Lin S, et al. Among authors: danishefsky sj. Angew Chem Int Ed Engl. 2001 May 18;40(10):1967-1970. Angew Chem Int Ed Engl. 2001. PMID: 11385688 No abstract available.
Concise Stereoselective Routes to Advanced Intermediates Related to Natural and Unnatural Pinnaic Acid This work was supported by the National Institutes of Health (Grant Numbers: CA28824). Postdoctoral Fellowship support is gratefully acknowledged by M.W.C. (U.S. Army BCRP, DAMD17-98-1-8154), M.F.H. (5T32 CA62948-05), and D.T. (Schering Research Foundation, Berlin). We thank Dr. George Sukenick of the MSKCC NMR Core Facility for NMR and mass spectral analyses.
Carson MW, Kim G, Hentemann MF, Trauner D, Danishefsky SJ. Carson MW, et al. Among authors: danishefsky sj. Angew Chem Int Ed Engl. 2001 Dec 3;40(23):4450-4452. doi: 10.1002/1521-3773(20011203)40:23<4450::aid-anie4450>3.0.co;2-m. Angew Chem Int Ed Engl. 2001. PMID: 12404442 No abstract available.
Total Synthesis and Proof of Stereochemistry of Natural and Unnatural Pinnaic Acids: A Remarkable Long-Range Stereochemical Effect in the Reduction of 17-Oxo Precursors of the Pinnaic Acids This work was supported by the National Institutes of Health (Grant Numbers: CA28824). Postdoctoral Fellowship support is gratefully acknowledged by M.W.C. (U.S. Army BCRP, DAMD17-98-1-8154). We thank Dr. George Sukenick of the MSKCC NMR Core Facility for NMR and mass spectral analyses. We would like to thank professor Nakanishi for his supportive interest in the project.
Carson MW, Kim G, Danishefsky SJ. Carson MW, et al. Among authors: danishefsky sj. Angew Chem Int Ed Engl. 2001 Dec 3;40(23):4453-4456. doi: 10.1002/1521-3773(20011203)40:23<4453::aid-anie4453>3.0.co;2-4. Angew Chem Int Ed Engl. 2001. PMID: 12404443 No abstract available.
322 results