Zobrazeno 1 - 10
of 63
pro vyhledávání: '"U K, Pandit"'
Publikováno v:
Recueil des Travaux Chimiques des Pays-Bas. 99:20-23
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::049532b0049d374b805acc6674b4fe41
https://doi.org/10.1002/recl.19800990106
https://doi.org/10.1002/recl.19800990106
Autor:
U. K. Pandit
Publikováno v:
Bulletin des Sociétés Chimiques Belges. 95:987-993
The chemistry and applications of models of tetrahydrofolate and pyridine nucleotide coenzymes are discussed.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5c65b7ace976806bd86cfe20adbe0552
https://doi.org/10.1002/bscb.19860951105
https://doi.org/10.1002/bscb.19860951105
Autor:
U. K. Pandit
Publikováno v:
ChemInform. 27
The total synthesis of sesbanimide A and its analogues has been achieved. The synthesized sesbanimides have been investigated for structure activity relationship. An approach has been developed for the synthesis of the antitumour alkaloid manzamine A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7876b0341484d2be56d59310fb20bed5
https://doi.org/10.1002/chin.199619292
https://doi.org/10.1002/chin.199619292
Autor:
U K, Pandit
Publikováno v:
Farmaco (Societa chimica italiana : 1989). 50(11)
The total synthesis of sesbanimide A and its analogues has been achieved. The synthesized sesbanimides have been investigated for structure activity relationship. An approach has been developed for the synthesis of the antitumour alkaloid manzamine A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::561c06047a798a9f1bbb501709c85954
https://pubmed.ncbi.nlm.nih.gov/8593171
https://pubmed.ncbi.nlm.nih.gov/8593171
Autor:
U. K. Pandit, A. Chatterjee
Publikováno v:
ChemInform. 21
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eb519ea5ca637a131dfe1e45abe1ca03
https://doi.org/10.1002/chin.199037318
https://doi.org/10.1002/chin.199037318
Autor:
U. K. Pandit, K. M. Brands
Publikováno v:
HETEROCYCLES. 30:257
L-Serine has been converted into a chiral pyrrolo[2,3]isoquinoline derivative which can serve as a potential intermediate for manzamines
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6293e4b9d24452a39f7bdcf27abba057
https://doi.org/10.3987/com-89-s20
https://doi.org/10.3987/com-89-s20
Publikováno v:
Synthetic Communications. 1:89-92
Dienamine I is a versatile intermediate for the total synthesis of modified steroids, Several examples of its application have been recently communicated from this laboratory3,4. We now wish to report the conversion of dienamine I into a 5,10-diazast
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ec12e10fba3e0d16b307f271fbf5ee15
https://doi.org/10.1080/00397917108081621
https://doi.org/10.1080/00397917108081621
Publikováno v:
Synthetic Communications. 2:345-351
Interest in non-glycosidic derivatives of the nucleo-bases uracil, theymine, cytosine, adenine and guanine stems from their status as nucleoside analogues. It is noteworty in this connection that the anti-biotics aristeromycin3 and eritadenine4 consi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0f186ca62aa6ae0a9e82e713d3c10a08
https://doi.org/10.1080/00397917208081778
https://doi.org/10.1080/00397917208081778
Publikováno v:
Synthetic Communications. 1:41-45
The replacement of the sugar notsty of nucleosides and nueleotides by suitaole molecular systems, provides novel models of nucleic acid corpoonents for pnysico and biochemical studies. Several such “unconVentioral” analogues, based upon α-amino
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d767106178d15adbd8a0bab69cd9619a
https://doi.org/10.1080/00397917108081615
https://doi.org/10.1080/00397917108081615
Publikováno v:
Journal of medicinal chemistry. 20(12)
Di-tert-butyl beta,beta-difluorooxaloacetate, prepared by fluorination of di-tert-butyl oxaloacetate with perchloryl fluoride, was converted to di-tert-butyl beta,beta-difluoroaspartate via its O-methyl oxime, followed by reduction. The tert-butyl es
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a3f5acc0189c633b62435feda7f2167f
https://pubmed.ncbi.nlm.nih.gov/592334
https://pubmed.ncbi.nlm.nih.gov/592334