Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Niranjan N. Pai"'
Publikováno v:
Drug Development and Industrial Pharmacy. 22:181-184
Co-drugs of the anti-inflammatory agents dexamethasone and prednisone, and antineoplastic agents melphalan and chbrambucil, were synthesized using an esterification reaction. The carboxylic acids were activated using dicyclohexylcarbodiimide (DCC) an
Publikováno v:
Natural Product Letters. 6:77-80
The characteristic metabolites of Quararibea funebris are based on (2S, 3S, 4R)-γ-hydroxyisoleucine, a hitherto rare amino acid. Two new stereoselective and efficient syntheses of this compound are described; one is based on Claisen chemistry and th
Autor:
Sheri L. Ablaza, Philip W. Le Quesne, Simon Bolvig, Ying Dong, David A. Forsyth, Shao-Xia Yu, Niranjan N. Pai
Publikováno v:
ChemInform. 30
Autor:
Niranjan N. Pai, Andre Rosowsky
Publikováno v:
Nucleosides and Nucleotides. 10:837-851
The 5′-O-(4,4′-dimethoxytrityl) and 5′-O-(tert-butyldimethylsilyl) derivatives of 2′-,3′-O-thiocarbonyl-6-azauridine and 2′,3′-O-thiocarbonyl-5-chlorouridine were synthesized from the parent nucleosides by reaction with 4, 4′-dimethox
Autor:
Philip W. Le Quesne, and David A. Forsyth, Shao-Xia Yu, Sheri L. Ablaza, Niranjan N. Pai, Simon Bolvig, Ying Dong
Publikováno v:
The Journal of organic chemistry. 64(8)
Syntheses of racemic forms of the main secondary metabolites of Quararibea funebris, (+/-)-funebrine, (+/-)-funebral, and their biogenetic precursor (+/-)-(2S,3S,4R)-gamma-hydroxyalloisoluecine lactone have been developed. In synthetic studies, a new
Autor:
Dong Y; Department of Chemistry and Barnett Institute, Northeastern University, Boston, Massachusetts 02115-5096., Niranjan N Pai N, Ablaza SL, Yu SX, Bolvig S, Forsyth DA, Le Quesne PW
Publikováno v:
The Journal of organic chemistry [J Org Chem] 1999 Apr 16; Vol. 64 (8), pp. 2657-2666.