Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Prosenjit Chattopadhyay"'
Publikováno v:
Organometallics. 30:1869-1873
The reaction of cobalt(III) octaethylcorrole (CoOEC) with ethyl diazoacetate (EDA) under a nitrogen atmosphere led to the formation of bridged complexes with the carbene moiety inserted into one of the cobalt−nitrogen bonds. The bridged complexes u
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a5ce942e8a763aab76983f12f6ca37f7
https://doi.org/10.1021/om101113x
https://doi.org/10.1021/om101113x
Publikováno v:
Tetrahedron Letters. 49:4640-4643
Synthesis and self-association studies of a uracil-2,6-diaminopyridine-lithocholic acid conjugate are described. The dimeric supramolecular structure is characterized by NMR spectroscopic, ESI-MS, and size exclusion chromatographic studies.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9ebd311f5a3411773c4d66215c5f84a8
https://doi.org/10.1016/j.tetlet.2008.05.069
https://doi.org/10.1016/j.tetlet.2008.05.069
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 17:1553-1557
Hydrogen-bonding interactions of steroid-based cyclic and acyclic receptors containing 2,6-bis(acylamino)pyridine with uracil derivatives were studied in CDCl3. Acyclic receptors show better binding behaviour as compared to cholaphanes with uracil de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c4d08f56d000c2ee494013c844831054
https://doi.org/10.1016/j.bmcl.2006.12.115
https://doi.org/10.1016/j.bmcl.2006.12.115
Publikováno v:
Tetrahedron. 62:8620-8624
Novel cholaphanes 6a,b, based on lithocholic and deoxycholic acids, were synthesised through 3a,b by a sequence of reactions involving Cs-salt methodology of macrocyclisation. Cholaphanes 6a,b and acyclic steroidal receptors 3a,b bind flavin analogue
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ab8d2ea1eb709a5b82818bb1755bf5e2
https://doi.org/10.1016/j.tet.2006.06.029
https://doi.org/10.1016/j.tet.2006.06.029
Publikováno v:
Synthetic Communications. 36:1857-1861
10‐Substituted isoalloxazines were synthesized in two steps starting from 1,2‐phenylenediamine. Monoalkylation of the diamine resulted in 2‐amino‐N‐alkylanilines, which were subsequently condensed with alloxan in boric acid and acetic acid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e02afc7b93928219a188d73420fd5d06
https://doi.org/10.1080/00397910600602552
https://doi.org/10.1080/00397910600602552
Publikováno v:
ChemInform. 37
10‐Substituted isoalloxazines were synthesized in two steps starting from 1,2‐phenylenediamine. Monoalkylation of the diamine resulted in 2‐amino‐N‐alkylanilines, which were subsequently condensed with alloxan in boric acid and acetic acid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d9608d0c9f83491973528da7520703b1
https://doi.org/10.1002/chin.200646203
https://doi.org/10.1002/chin.200646203
Publikováno v:
Australian Journal of Chemistry. 61:216
The recognition properties of 7,8-dimethyl flavin analogues by bile acid-based receptors that contain 2,6-diaminopyridine and the dioctylamide of 2,6-diaminopyridine in CHCl3 were determined. The results show that the bile acid-based receptors bind 7
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e050ca19126363d63b53ef8d64709c69
https://doi.org/10.1071/ch07342
https://doi.org/10.1071/ch07342