Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Neal J. Green"'
Autor:
Paul R. Blakemore, Christine S. Nylund Kolz, Neal J. Green, James D. White, E Bryan Hauser, Linda E Keown, Mark A. Holoboski, Barton W. Phillips
Publikováno v:
The Journal of Organic Chemistry. 67:7750-7760
Rhizoxin D (2) was synthesized from four subunits, A, B, C, and D representing C3-C9, C10-C13, C14-C19, and C20-C27, respectively. Subunit A was prepared by cyclization of iodo acetal 21, which set the configuration at C5 of 2 through a stereoselecti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6645d54b150ffcbcba7aa3a764af9752
https://doi.org/10.1021/jo020537q
https://doi.org/10.1021/jo020537q
Publikováno v:
Tetrahedron Letters. 38:7333-7336
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3238ee517963b5d98690d41a5a8b226e
https://doi.org/10.1016/s0040-4039(97)01781-4
https://doi.org/10.1016/s0040-4039(97)01781-4
Publikováno v:
Tetrahedron Letters. 38:7329-7332
An asymmetric synthesis of the C3C13 segment of rhizoxin is described in which the relative stereochemistry of C7 and C8 is established through a chelation-controlled allylation followed by Mitsunobu inversion, and the pyran ring is constructed by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::29c9170d7ba8a53ff5e77047db878495
https://doi.org/10.1016/s0040-4039(97)01780-2
https://doi.org/10.1016/s0040-4039(97)01780-2
Publikováno v:
Journal of the American Chemical Society. 116:10450-10462
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9bcea9691da8d8b19855a872fb74b332
https://doi.org/10.1021/ja00102a011
https://doi.org/10.1021/ja00102a011
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::992a53f0dec18a5e8faa17a922b245a0
https://doi.org/10.1002/chin.199144285
https://doi.org/10.1002/chin.199144285
Autor:
Neal J. Green, Arthur G. Schultz
Publikováno v:
ChemInform. 22
Ortho-lithiation-alkylation of tertiary benzamide provides a series of 2-substituted chiral benzamides 3a-g. Birch reduction of 3a-j followed by alkylation of the resulting chiral amide enolate with MeI at −78°C gives 1,6-dialkyl-1,4-cyclohexadien
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::897674080d5b61bcce9353fe61f6e62d
https://doi.org/10.1002/chin.199142127
https://doi.org/10.1002/chin.199142127
Autor:
Arthur G. Schultz, Neal J. Green
Publikováno v:
ChemInform. 23
4-Carbomethoxy-4-vinyl-2,5-cyclohexadien-1-ones 6a and 6b were prepared from methyl benzoate and methyl 2-methoxybenzoate in 45% overall yields. Irradiation of 6a in benzene solution at 366 nm gave 2-carbometboxybicyclo- [3 2,3,4 .2 6,7 ]-2,6-octadie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6beac4f6d808abd2e66129b23f3e2720
https://doi.org/10.1002/chin.199226077
https://doi.org/10.1002/chin.199226077
Publikováno v:
ChemInform. 24
1,1,1-Trifluoroethyl esters of ω-hydroxycarboxylic acids were prepared and their conversion to macrocyclic lactones, including ricinelaidic lactone, was studied in the presence of catalytic quantities of tin(IV) reagents; a mechanism involving excha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::76444606a922a847d294cfea68b244f1
https://doi.org/10.1002/chin.199333208
https://doi.org/10.1002/chin.199333208
Publikováno v:
ChemInform. 29
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::453f946da6803ba9677f6bbc9e5f9636
https://doi.org/10.1002/chin.199805229
https://doi.org/10.1002/chin.199805229
Autor:
Arthur G. Schultz, Neal J. Green
Publikováno v:
Journal of the American Chemical Society. 114:1824-1829
4-Carbomethoxy-4-vinyl-2,5-cyclohexadien-1-ones 6a and 6b were prepared from methyl benzoate and methyl 2-methoxybenzoate in 45% overall yields. Irradiation of 6a in benzene solution at 366 nm gave 2-carbometboxybicyclo- [3 2,3,4 .2 6,7 ]-2,6-octadie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0812fd18065060797334d7ddbdb1c085
https://doi.org/10.1021/ja00031a042
https://doi.org/10.1021/ja00031a042