Zobrazeno 1 - 10
of 10
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d4b2c2504aac4eb3e60cb5b2456c7f50
https://doi.org/10.3109/03639049609041989
https://doi.org/10.3109/03639049609041989
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::473a972072e62466459d2b204156df4a
https://doi.org/10.1080/10575639508044091
https://doi.org/10.1080/10575639508044091
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5564502ae39910772b837532e8101c27
https://doi.org/10.1002/chin.199933241
https://doi.org/10.1002/chin.199933241
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e702eff3325c47216eb465e105073b12
https://doi.org/10.1080/07328319108046665
https://doi.org/10.1080/07328319108046665
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8f186a2ba9fa48b96489606b61bfa3f
https://pubmed.ncbi.nlm.nih.gov/11674333
https://pubmed.ncbi.nlm.nih.gov/11674333
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.
Publikováno v:
Drug Development & Industrial Pharmacy; 1996, Vol. 22 Issue 2, p181-184, 4p
Autor:
Rosowsky, Andre, Pai, Niranjan N.
Publikováno v:
Nucleosides & Nucleotides; Jun1991, Vol. 10 Issue 4, p837-851, 15p
Publikováno v:
Natural Product Letters; Feb1995, Vol. 6 Issue 1, p77-80, 4p
Autor:
Surya K. De
An indispensable guide for all synthetic chemists who want to learn about the most relevant reactions and reagents employed to synthesize important heterocycles and drugs! The synthesis of natural products, bioactive compounds, pharmaceuticals, and d
