Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Thomas J. Fleck"'
Autor:
Vikas Sikervar, Thomas J. Fleck
Publikováno v:
e-EROS Encyclopedia of Reagents for Organic Synthesis
[1088-00-2] C18H13P (MW 260.28) InChI = 1S/C18H13P/c1-2-8-14(9-3-1)19-17-12-6-4-10-15(17)16-11-5-7-13-18(16)19/h1-13H InChIKey = DNPJAMMRVRYLOB-UHFFFAOYSA-N (synthesis of phosphorus compounds required for Wittig reactions;1 ring expansion to the dibe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f0beed770f9b15d4fa2d766bb5ff38c3
https://doi.org/10.1002/047084289x.rp061.pub2
https://doi.org/10.1002/047084289x.rp061.pub2
Publikováno v:
Organic Process Research & Development. 10:334-338
FeCl3 catalyzed an isomerization-free Friedel−Crafts sulfonylation between 1-naphthalenesulfonyl chloride and halobenzenes. The coupled halide was then displaced using 35% hydrazine in DMSO to provide the Fischer indole precursor. Pure 5-chloro-2-p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3f4be6c6c3216c0d84871c86bd3974ec
https://doi.org/10.1021/op050208a
https://doi.org/10.1021/op050208a
Publikováno v:
Journal of the American Chemical Society. 115:6078-6093
The total synthesis of (-)-chaparrinone (3), (-)-glaucarubolone (4), and (+)-glaucarubinone (3) is described. The synthesis features an intermolecular Diels-Alder reaction between dienophile 6 and (E)-4-methyl-3,5-hexadienoic acid (17) in 5.0 M lithi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::acc96019b196a8af2fe4516c9a72b29c
https://doi.org/10.1021/ja00067a025
https://doi.org/10.1021/ja00067a025
Publikováno v:
ChemInform. 24
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::93775674315352b4c2eaae1afdf59b48
https://doi.org/10.1002/chin.199348223
https://doi.org/10.1002/chin.199348223
Autor:
Paul A. Grieco, Thomas J. Fleck
Publikováno v:
Tetrahedron Letters. 33:1813-1816
The first total synthesis of (±)-glaucarubolone ( 1 ) and (±)-holacanthone ( 2 ) is detailed which commences with tetracyclic alcohol 3 .
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7ef5c2698db7a2d2544b618a3fdb74ab
https://doi.org/10.1016/s0040-4039(00)74149-9
https://doi.org/10.1016/s0040-4039(00)74149-9
Publikováno v:
The Journal of organic chemistry. 68(25)
N-Methyl-N-[(1S)-1-[(3R)-pyrrolidin-3-yl]ethyl]amine (1)(1) is a key intermediate in the preparation of premafloxacin (2), which was under development as an antibiotic for use against pathogens of veterinary importance. This paper describes the devel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24471d06d81b85c7add83a314a0d3241
https://pubmed.ncbi.nlm.nih.gov/14656085
https://pubmed.ncbi.nlm.nih.gov/14656085
Autor:
Thomas J. Fleck
Publikováno v:
e-EROS Encyclopedia of Reagents for Organic Synthesis
Ph2SiH2 [775-12-2] C12H12Si (MW 184.33) InChI = 1S/C12H12Si/c1-3-7-11(8-4-1)13-12-9-5-2-6-10-12/h1-10H,13H2 InChIKey = VDCSGNNYCFPWFK-UHFFFAOYSA-N CsF [13400-13-0] CsF (MW 151.91) InChI = 1S/Cs.FH/h;1H/q+1;/p-1 InChIKey = XJHCXCQVJFPJIK-UHFFFAOYSA-M
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::43d2a764c3f4e35608a4a1c38ebd8155
https://doi.org/10.1002/047084289x.rp101
https://doi.org/10.1002/047084289x.rp101
Autor:
Thomas J. Fleck
Publikováno v:
e-EROS Encyclopedia of Reagents for Organic Synthesis
[36121-19-4] C13H30FP (MW 236.40) InChI = 1S/C13H30FP/c1-5-8-11-15(4,14,12-9-6-2)13-10-7-3/h5-13H2,1-4H3 InChIKey = LQJPONADDGDFAF-UHFFFAOYSA-N (fluorinating reagent1-3 and fluoride source for silicon displacement1) Alternate Names: tributyl(methyl)p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b30b81c595f134bdc6530bf7e4b44884
https://doi.org/10.1002/047084289x.rf016
https://doi.org/10.1002/047084289x.rf016