Zobrazeno 1 - 10
of 259
pro vyhledávání: '"DE LERA AR"'
Publikováno v:
Nutrition reviews
Nutrition reviews, 2018, 76 (12), pp.929-941. ⟨10.1093/nutrit/nuy057⟩
Nutrition reviews, 2018, 76 (12), pp.929-941. ⟨10.1093/nutrit/nuy057⟩
The identity of the endogenous RXR ligand has not been conclusively determined, even though several compounds of natural origin, including retinoids and fatty acids, have been postulated to fulfill this role. Filling this gap, 9-cis-13,14-dihydroreti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d447696821d50706c658c00c45958b37
https://hal.science/hal-03670944
https://hal.science/hal-03670944
Publikováno v:
Organic Letters. 10:77-80
A three-step mechanism involving the formation and rearrangement of an intermediate with indoline-azetidine spirocyclic core structure was shown by DFT computations to account for the electrophilic cyclization of tryptophan derivatives to hexahydropy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6bd7484b9d1d837f736993f86ec35d86
https://doi.org/10.1021/ol702732j
https://doi.org/10.1021/ol702732j
Publikováno v:
Organic Letters. 6:901-904
[reaction: see text] Only conrotatory transition structures were located by B3LYP6-311++G(3df, 2p) computations for the electrocyclic ring opening of cyclopropyl anions having different substituents (H, Me, CN). The transition structure for the simil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dbdbf99d8d6231e0ea96b8ca0061c82c
https://doi.org/10.1021/ol036448x
https://doi.org/10.1021/ol036448x
Publikováno v:
The Journal of Organic Chemistry. 65:2696-2705
A domino reaction that is pericyclic in nature is thought to be triggered upon treatment of alkenynol 10 with arylsulfenyl chlorides. The process comprises an ordered sequence of sigmatropic rearrangements: a reversible [2,3]-allyl sulfenate to allyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::992b326b17922b2f89af0ac83839bcc9
https://doi.org/10.1021/jo991757f
https://doi.org/10.1021/jo991757f
Publikováno v:
Scopus-Elsevier
Conventional Horner-Wadsworth-Emmons and Wittig condensations were used to fluorinate the odd-numbered positions of the retinal side chain past C(7). The stereochemically labile cis-fluororetinals were easily converted into the most stable trans-fluo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c03a29c2518671df3eb387cf9896bb9
https://doi.org/10.1021/jo961355x
https://doi.org/10.1021/jo961355x
Publikováno v:
Expert opinion on therapeutic patents. 21(1)
Retinoids are currently used in the clinic for the treatment of skin diseases and acute promielocytic leukemia and are known to contribute to early development and organogenesis in embryo and throughout life. Most of these activities are primarily du
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6aa0088019ca01716553a0709aa763b
https://pubmed.ncbi.nlm.nih.gov/21091043
https://pubmed.ncbi.nlm.nih.gov/21091043
Publikováno v:
The Journal of organic chemistry. 65(19)
Analogues of 9-cis-retinoic acid with locked 6-s-cis and 6-s-trans conformations have been stereoselectively synthesized using a Stille coupling reaction between bicyclic dienyl triflates (5and 6, respectively) and (Z)-tributylstannylbut-2-en-1-ol (7
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0fcded0c23cbface9438ad53be66f48
https://pubmed.ncbi.nlm.nih.gov/10987922
https://pubmed.ncbi.nlm.nih.gov/10987922
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Akademický článek
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