Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Eric J. May"'
Autor:
Adam T. Froemming, Lyndsay D. Viers, Eric J. May, Boyd R. Viers, Akira Kawashima, Eugene D. Kwon, R. Jeffrey Karnes
Publikováno v:
Abdominal Radiology. 41:862-876
Recurrent prostate cancer following primary treatment is common, and the population of men with biochemical recurrence is complex. Conventional management of recurrent prostate cancer involves nontargeted and/or systemic therapies, without defining a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2727cd49498b7e130f80509c37c64e7
https://doi.org/10.1007/s00261-015-0562-1
https://doi.org/10.1007/s00261-015-0562-1
Publikováno v:
Helvetica Chimica Acta. 88:1397-1404
Bifunctional vinyl ethers react with electron-poor alkenes to cyclobutanes in good yields. The second CC bond reacted with neither the cyclobutane nor its zwitterion intermediate, even on heating. Cyclobutanes formed from ‘tetracyanoethylene’ (8)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::94455a82e349eb925aa54d676c2d2e38
https://doi.org/10.1002/hlca.200590112
https://doi.org/10.1002/hlca.200590112
Publikováno v:
Tetrahedron Letters. 38:4333-4336
Cu(I)Cl decomposition of the phenyliodonium ylides derived from o-, m- and p-methoxyphenyl-3-ketopentanoic acid methyl esters affords the corresponding 5-, 6- and 7-methoxy-1-carbomethoxy-2-tetralones in preparative yields. The lower homologous pheny
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6e6c02492793654c8b98141065dabd5a
https://doi.org/10.1016/s0040-4039(97)00967-2
https://doi.org/10.1016/s0040-4039(97)00967-2
Autor:
Eric J. May, Michael P. Doyle
Publikováno v:
Synlett. 2001:0967-0969
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::af50003915ced48e5d4ddcd8dca8cf48
https://doi.org/10.1055/s-2001-14635
https://doi.org/10.1055/s-2001-14635
Publikováno v:
ChemInform. 28
Cu(I)Cl decomposition of the phenyliodonium ylides derived from o-, m- and p-methoxyphenyl-3-ketopentanoic acid methyl esters affords the corresponding 5-, 6- and 7-methoxy-1-carbomethoxy-2-tetralones in preparative yields. The lower homologous pheny
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1a0d07f7f894b85e3e0c09ccdec4ffe4
https://doi.org/10.1002/chin.199738068
https://doi.org/10.1002/chin.199738068
Publikováno v:
ChemInform. 29
Iodonium ylides of methyl 3-oxo- trans,trans -6,8-tetradecadienoate ( 1 ) and diprotected methyl 3,5-di(t-butyldimethyl-silyloxy)-2,6,8-tetrahecatrieneoate ( 5 ) undergo regio- and stereoselective intramolecular cyclopropanation with Cu(I)Cl catalysi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cf7c36f1949e5abeae35763f187c1a92
https://doi.org/10.1002/chin.199819082
https://doi.org/10.1002/chin.199819082
Publikováno v:
ChemInform. 30
Fused cyclopentane derivatives, viz. methyl 2-oxobicyclo[3.1.0]hexane-1-carboxylate (2a), methyl 6-methyl-2-oxobicyclo[3.1.0]hexane-1-carboxylate (2b) and methyl 3-oxotricyclo[3.3.0.0 2,8 ]octane-2-carboxylate (6), have been functionalized by using t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::42631d7c20bdb5d67d0adf99a6be7ec3
https://doi.org/10.1002/chin.199906075
https://doi.org/10.1002/chin.199906075
Publikováno v:
The Journal of organic chemistry. 66(24)
Diazo decomposition of steroidal diazoacetates, where the point of attachment is the 3-position of the steroid A-ring, catalyzed by chiral dirhodium(II) carboxamidates results in products from carbon-hydrogen insertion in high yield and selectivities
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dd42fe56bc8093890688eac9493cbef0
https://pubmed.ncbi.nlm.nih.gov/11722213
https://pubmed.ncbi.nlm.nih.gov/11722213
Publikováno v:
Tetrahedron Letters. 39:765-766
Iodonium ylides of methyl 3-oxo- trans,trans -6,8-tetradecadienoate ( 1 ) and diprotected methyl 3,5-di(t-butyldimethyl-silyloxy)-2,6,8-tetrahecatrieneoate ( 5 ) undergo regio- and stereoselective intramolecular cyclopropanation with Cu(I)Cl catalysi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0dd4f0e621113cbb40b895f596983740
https://doi.org/10.1016/s0040-4039(97)10620-7
https://doi.org/10.1016/s0040-4039(97)10620-7
Publikováno v:
Journal of Chemical Research. :32-33
Fused cyclopentane derivatives, viz. methyl 2-oxobicyclo[3.1.0]hexane-1-carboxylate (2a), methyl 6-methyl-2-oxobicyclo[3.1.0]hexane-1-carboxylate (2b) and methyl 3-oxotricyclo[3.3.0.0 2,8 ]octane-2-carboxylate (6), have been functionalized by using t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1ede07c042afd2b7508ddf3793904e7b
https://doi.org/10.1039/a701440f
https://doi.org/10.1039/a701440f