Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Pamela Albaugh"'
Autor:
John F. Tallman, Geoff White, Matt Crago, Lu Marshall, James V. Cassella, Pamela Albaugh, James Gregory, Dorothy W. Gallagher, Hutchison Alan J, Phil C. Ross
Publikováno v:
Journal of medicinal chemistry. 45(23)
Benzodiazepines are allosteric modulators of the GABA(A) receptor. The traditionally prescribed benzodiazepines are nonselective and suffer from numerous side effects. Upon the identification of receptor subtypes, we set out to discover selective age
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::04641cdecffd8a06d387d6a2237e6fb3
https://pubmed.ncbi.nlm.nih.gov/12408715
https://pubmed.ncbi.nlm.nih.gov/12408715
Publikováno v:
Tetrahedron Letters. 23:723-726
Ethyl 3-methyl-2-trimethylsilyl-3-butenoate ( 3 ) undergoes reaction selectively at carbon 4, upon treatment with a Lewis acid and carbonyl compounds, acetals/ketals, acid chlorides, and chloromethyl phenyl sulfide. This overall conversion represents
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::40d6a4b2c5ed9db228e8075949baee7a
https://doi.org/10.1016/s0040-4039(00)86931-2
https://doi.org/10.1016/s0040-4039(00)86931-2
Publikováno v:
The Journal of Organic Chemistry. 48:5288-5302
Preparation d'un certain nombre d'esters du type methyl-3 trimethylsilyl-2 butene-3oate d'ethyle et etude de leurs reactions avec divers electrophiles (aldehydes, cetones, acetals, chlorures d'acyle etc.) en presence d'acides de Lewis (TiCl 4 et trif
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9efbb04ea740a9ca5fc9a1863bcb3d53
https://doi.org/10.1021/jo00174a026
https://doi.org/10.1021/jo00174a026
Publikováno v:
Tetrahedron. 41:5861-5869
Treatment of the readily prepared enzymes 12, 21 and 45 with Co2(CO) at ca 110° results in high yields (80%) of substituted bicyclo[3.3.0]octenones, that are suitable for straightforward elaboration into coriolin and hirsutic acid precursors. A mech
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6d1f8d03ac6f09177a33ec380eb63aa2
https://doi.org/10.1016/s0040-4020(01)91425-5
https://doi.org/10.1016/s0040-4020(01)91425-5
Publikováno v:
J. Chem. Soc., Chem. Commun.. :804-806
Intramolecular cyclization of the methoxyallene–alkoxide adducts (1a) proceeds along two different pathways via a methoxyallyl radical to give either a dihydrofuran, or vinyl epoxide, depending upon the steric environment of the redical anion.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0d18d7a8f0aa5073d841c8c42f918024
https://doi.org/10.1039/c39840000804
https://doi.org/10.1039/c39840000804
Publikováno v:
Chemischer Informationsdienst. 15
Intramolecular cyclization of the methoxyallene–alkoxide adducts (1a) proceeds along two different pathways via a methoxyallyl radical to give either a dihydrofuran, or vinyl epoxide, depending upon the steric environment of the redical anion.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d1e1ea9f45ed3d60a32c15e0fae96e87
https://doi.org/10.1002/chin.198445092
https://doi.org/10.1002/chin.198445092
Publikováno v:
Journal of the American Chemical Society. 101:5435-5436
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7444bd0872c189c4507d00ef2dabadc5
https://doi.org/10.1021/ja00512a065
https://doi.org/10.1021/ja00512a065