Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Howard Sard"'
Publikováno v:
The Journal of Organic Chemistry. 65:9261-9264
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e584b3699094e49326c18f18b2f8d150
https://doi.org/10.1021/jo001316s
https://doi.org/10.1021/jo001316s
Publikováno v:
Tetrahedron Letters. 44:4589-4591
General indole C 3 reductive alkylation conditions have been developed. The scope of this reaction includes C 2 unsubstituted indoles, aryl and alkyl aldehydes, as well as N–H and N -alkyl indole substrates.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3763857bc532033e0d255be2bed84797
https://doi.org/10.1016/s0040-4039(03)01010-4
https://doi.org/10.1016/s0040-4039(03)01010-4
Autor:
Marina W.H. Shen, Mario D. Gonzalez, John C. McKew, Wen Zhang, Tam Steve Yik-Kai, Howard Sard, Kun Wu, Soo Peang Khor, Paresh Thakker, Mark L. Behnke, Shanghao Liu, Megan A. Foley, Frank Lovering, Fuk-Wah Sum, Anu Mahadevan, James D. Clark
Publikováno v:
Journal of medicinal chemistry. 49(1)
Compound 1 was previously reported to be a potent inhibitor of cPLA(2)alpha in both artificial monomeric substrate and cell-based assays. However, 1 was inactive in whole blood assays previously used to characterize cyclooxygenase and lipoxygenase in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c97c459eda2a1b8504a723428c64b087
https://pubmed.ncbi.nlm.nih.gov/16392799
https://pubmed.ncbi.nlm.nih.gov/16392799
Autor:
Howard Sard
Publikováno v:
e-EROS Encyclopedia of Reagents for Organic Synthesis
[13698-16-3] C3H5Cl2NO2 (MW 157.98) InChI = 1S/C3H5Cl2NO2/c1-2-8-3(7)6(4)5/h2H2,1H3 InChIKey = PCGGNOFZZFFFLU-UHFFFAOYSA-N (stable but reactive pseudohalogen which adds to alkenes to give β-chlorocarbamates;1 useful for the chlorination of tertiary
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b370990b15f5fd25c4d5ab001cd0f30e
https://doi.org/10.1002/047084289x.rd138
https://doi.org/10.1002/047084289x.rd138
Publikováno v:
Tetrahedron. 37:3943-3950
The lithium and potassium salts of 2-vinylcyclobutanols undergo vinylcyclobutane rearrangement at 25–70°, providing an efficient method for the synthesis of 3-cyclohexenol derivatives. 2-Vinylcyclobutanones are prepared from α,β-unsaturated carb
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::55d04f25684c2dc37f5d0e3b414bd427
https://doi.org/10.1016/s0040-4020(01)93268-5
https://doi.org/10.1016/s0040-4020(01)93268-5
Autor:
Howard Sard, Rick L. Danheiser
Publikováno v:
Tetrahedron Letters. 24:23-26
Alkynylsilanes undergo regioselective [2+2] cycloadditions with dichloroketene in good yield; the regiochemical course of these reactions is in accord with frontier molecular orbital predictions.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0e33c20ea8c683264b413aff0162092d
https://doi.org/10.1016/s0040-4039(00)81316-7
https://doi.org/10.1016/s0040-4039(00)81316-7
Publikováno v:
Synthetic Communications. 13:813-816
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::920eb46df65de189fbcbb85ebe4370ce
https://doi.org/10.1080/00397918308063715
https://doi.org/10.1080/00397918308063715
Autor:
Howard Sard, Rick L. Danheiser
Publikováno v:
The Journal of Organic Chemistry. 45:4810-4812
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::776fe2f505a9bc3a88b84d42ee87ff63
https://doi.org/10.1021/jo01311a065
https://doi.org/10.1021/jo01311a065