Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Rosy Mallik"'
Publikováno v:
Molecules, Vol 26, Iss 14, p 4320 (2021)
Biologically important, chiral natural products of butenolides, (−)-blastmycinolactol, (+)-blastmycinone, (−)-NFX-2, (+)-antimycinone, lipid metabolites, (+)-ancepsenolide, (+)-homoancepsenolide, mosquito larvicidal butenolide and their analogues
Externí odkaz:
https://doaj.org/article/90738a54e40d4dcebbd33c36719a54df
Autor:
Santosh K. Nanda, Rosy Mallik
Publikováno v:
Asian Journal of Organic Chemistry. 11
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a918bf542eea025e79532ce18a4977e8
https://doi.org/10.1002/ajoc.202100552
https://doi.org/10.1002/ajoc.202100552
Autor:
Santosh K. Nanda, Rosy Mallik
Publikováno v:
Chemistry – A European Journal. 27
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9d7390c017dec1e8a190ccb076b5531c
https://doi.org/10.1002/chem.202186362
https://doi.org/10.1002/chem.202186362
Autor:
Rosy Mallik, Santosh K. Nanda
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 27(63)
Oxygen-bearing motifs, mainly the congener heterocycles are ubiquitous due to their presence in various natural products and bioactive scaffolds. Although in literature, several strategies have been developed for their synthesis, hydroalkoxylation of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9fa77a4a54ed3ea7b72b01a25c061f05
https://pubmed.ncbi.nlm.nih.gov/34343374
https://pubmed.ncbi.nlm.nih.gov/34343374
Publikováno v:
Synlett. 28:1209-1213
A route to the oxabicyclic cores of the HIV cytoprotective quinolone alkaloids, waltheriones C and D, is described. The approach relies on a stereospecific transannular bromoetherification followed by reductive debromination. The route can also be re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cb5cc8bf884ecb762567df55c5e27193
https://doi.org/10.1055/s-0036-1588150
https://doi.org/10.1055/s-0036-1588150
Publikováno v:
Tetrahedron Letters. 52:38-41
A rapid access to the central 4,5,6-tricyclic core of 4,5,6-trinems has been achieved by employing the alkyne [2+2+2]-cyclotrimerization as the key and final reaction in the synthesis.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::472cc4b4ecf16272ded9cdbd834564b8
https://doi.org/10.1016/j.tetlet.2010.10.123
https://doi.org/10.1016/j.tetlet.2010.10.123
Publikováno v:
Tetrahedron Letters. 50:4844-4847
A preliminary study dealing with the Pd-mediated alkynediol cycloisomerization to construct the central bicyclic ketal core of cyclodidemniserinol trisulfate is documented.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c3c954a3b57f618cb6a4d552509fce56
https://doi.org/10.1016/j.tetlet.2009.06.023
https://doi.org/10.1016/j.tetlet.2009.06.023
Publikováno v:
Tetrahedron Letters. 47:3649-3652
Functionalized bicyclic enol-ethers and spiroketals are prepared by Pd catalyzed cycloisomerization of 3-C-alkynylfuranosyl derivatives. Cycloisomerization of differently substituted alkyne derivatives revealed a preference for 6-endo-dig cyclization
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bced059ccd441554ef18b3ff587e4fa4
https://doi.org/10.1016/j.tetlet.2006.03.143
https://doi.org/10.1016/j.tetlet.2006.03.143
Publikováno v:
ChemInform. 42
A rapid access to the central 4,5,6-tricyclic framework of cyclonorcardinin trinems employing an alkyne [2 + 2 + 2] cyclotrimerization reaction is given.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f88e2e6a85aea18a25497784a0ebb627
https://doi.org/10.1002/chin.201114210
https://doi.org/10.1002/chin.201114210
Publikováno v:
ChemInform. 39
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f57c25bf5dae2df5263b2ed1db144e1e
https://doi.org/10.1002/chin.200817194
https://doi.org/10.1002/chin.200817194