Zobrazeno 1 - 10
of 13
pro vyhledávání: '"David J. Madar"'
Publikováno v:
Canadian Journal of Chemistry. 79:1711-1726
Selective syntheses of the highly substituted bromonaphthoates 4a, 4b, 19, and 22 are reported. These compounds were targeted as precursors to the naphthoquinone nucleus of damavaricin D; compound 22 ultimately was used in the successful total synthe
Publikováno v:
Journal Of The Brazilian Chemical Society. 7:327-334
Autor:
William R. Roush, David J. Madar
Publikováno v:
Tetrahedron Letters. 34:1553-1556
The highly functionalized streptovaricin-damavaricin D aromatic precursors 12 and 15 have been prepared and coupled with propionaldehyde or unsaturated aldehydes 16 and 18 via aryllithium intermediates to give 2, 3 and 19.
Publikováno v:
ChemInform. 29
Publikováno v:
ChemInform. 33
Selective syntheses of the highly substituted bromonaphthoates 4a, 4b, 19, and 22 are reported. These com- pounds were targeted as precursors to the naphthoquinone nucleus of damavaricin D; compound 22 ultimately was used in the successful total synt
Publikováno v:
e-EROS Encyclopedia of Reagents for Organic Synthesis
1 l-(R,R)-tartrate (E)-crotyl [99745-86-5] C14H23BO6 (MW 298.14) InChI = 1S/C14H23BO6/c1-6-7-8-15-20-11(13(16)18-9(2)3)12(21-15)14(17)19-10(4)5/h6-7,9-12H,8H2,1-5H3/b7-6+/t11-,12-/m1/s1 InChIKey = UQRUTCGBDPMECL-BYAJROORSA-N d-(S,S), (Z) [99687-40-8]
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::36df9460671207ccd94d74954b0236ff
https://doi.org/10.1002/047084289x.rd251.pub2
https://doi.org/10.1002/047084289x.rd251.pub2
Autor:
David J. Madar, Daisy Pireh, Elizabeth H. Fry, K.L. Longenecker, C. Jakob, Paul E. Wiedeman, Thomas H. Lubben, K.D. Stewart, Sherwin Wilk, Zhonghua Pei, Chun W. Lin, Vincent S. Stoll, Hong Yong, Thomas W. Von Geldern, Michael A. Stashko, James M. Trevillyan, Stephen J. Ballaron, Fatima Basha
Publikováno v:
Biochemistry. 45(24)
Dipeptidyl peptidase IV (DPP-IV) belongs to a family of serine peptidases, and due to its indirect regulatory role in plasma glucose modulation, DPP-IV has become an attractive pharmaceutical target for diabetes therapy. DPP-IV inactivates the glucag
Autor:
David J. Madar
Publikováno v:
e-EROS Encyclopedia of Reagents for Organic Synthesis
[14470-28-1] C20H17ClO (MW 308.81) InChI = 1S/C20H17ClO/c1-22-19-14-12-18(13-15-19)20(21,16-8-4-2-5-9-16)17-10-6-3-7-11-17/h2-15H,1H3 InChIKey = OBOHMJWDFPBPKD-UHFFFAOYSA-N (reagent used for the protection of hydroxyl and amino groups1) Alternate Nam
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::44cfdfd4e3a0c238dc92f23d9237095a
https://doi.org/10.1002/047084289x.rn00130
https://doi.org/10.1002/047084289x.rn00130
Autor:
David J. Madar
Publikováno v:
e-EROS Encyclopedia of Reagents for Organic Synthesis
[40615-36-9] C21H19ClO2 (MW 338.83) InChI = 1S/C21H19ClO2/c1-23-19-12-8-17(9-13-19)21(22,16-6-4-3-5-7-16)18-10-14-20(24-2)15-11-18/h3-15H,1-2H3 InChIKey = JBWYRBLDOOOJEU-UHFFFAOYSA-N (reagent used for the protection of hydroxyl, amino, and sulfhydryl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ea02b81039a27d4c1746d9c7fcf89bb4
https://doi.org/10.1002/047084289x.rn00131
https://doi.org/10.1002/047084289x.rn00131