Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Melissa V. Deaton"'
Publikováno v:
Tetrahedron Letters. 43:399-402
The treatment of N -benzylated heterocycles with potassium tert -butoxide/DMSO and oxygen at room temperature cleanly affords N -debenzylated products in high yield. This procedure can be utilized on a variety of functionalized nitrogen-containing he
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::97b98a896c1022eb7e65561c7fc804c7
https://doi.org/10.1016/s0040-4039(01)02192-x
https://doi.org/10.1016/s0040-4039(01)02192-x
Publikováno v:
Tetrahedron. 53:16299-16312
A catalytic ene-like reaction of aldehydes with those vinyl ethers that display the oxygen functionality at the central carbon of an allylic system, e.g., 2-methoxypropene, is discussed in detail. The reaction is promoted by 0.05 equiv. of the 1:1 co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4cd772ae69a3eb8b6e849a440ecd6442
https://doi.org/10.1016/s0040-4020(97)01016-8
https://doi.org/10.1016/s0040-4020(97)01016-8
Publikováno v:
The Journal of Organic Chemistry. 62:7806-7811
(±)-Phyllanthocin has been synthesized through a key step involving the enelike reaction of an aldehyde with 2-methoxypropene recently developed in these laboratories. This work demonstrates that our chemistry is suitable for multistep synthetic app
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e2050d052ca9dc4528b43c3f43a49934
https://doi.org/10.1021/jo971151w
https://doi.org/10.1021/jo971151w
Publikováno v:
Tetrahedron Letters. 38:4355-4358
Benzazocenone intermediates for mitomycinoids are now available in only six steps. Key phases of this sequence include the ene-like reaction of 2-methoxypropene with a 2-azidophenyacetaldehyde and a novel heterocyclic ring formation/expansion reactio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::633081b329252234e4637f84741a809f
https://doi.org/10.1016/s0040-4039(97)00933-7
https://doi.org/10.1016/s0040-4039(97)00933-7
Autor:
Marco A. Ciufolini, Melissa V. Deaton
Publikováno v:
Tetrahedron Letters. 34:2409-2412
Catalytic amounts of Yb(fod) 3 catalyze a bimolecular ene-like reaction between ordinary aldehydes and vinyl ethers, in which the oxygen functionality is located at the central carbon of an allylic system. These reactions proceed at room temperature
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c257ffb50423a591a124515317ff418a
https://doi.org/10.1016/s0040-4039(00)60428-8
https://doi.org/10.1016/s0040-4039(00)60428-8
Autor:
Marco A. Ciufolini, Melissa V. Deaton
Publikováno v:
ChemInform. 24
Catalytic amounts of Yb(fod) 3 catalyze a bimolecular ene-like reaction between ordinary aldehydes and vinyl ethers, in which the oxygen functionality is located at the central carbon of an allylic system. These reactions proceed at room temperature
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::60b63dea6542fc577e2d0cec9c48e347
https://doi.org/10.1002/chin.199336138
https://doi.org/10.1002/chin.199336138
Publikováno v:
ChemInform. 28
Benzazocenone intermediates for mitomycinoids are now available in only six steps. Key phases of this sequence include the ene-like reaction of 2-methoxypropene with a 2-azidophenyacetaldehyde and a novel heterocyclic ring formation/expansion reactio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::14db461d65d896ae05f8e6cdf4c9aa0a
https://doi.org/10.1002/chin.199738210
https://doi.org/10.1002/chin.199738210
Publikováno v:
ChemInform. 29
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::60b2b802ad4857c4dbb0100f3b1e7345
https://doi.org/10.1002/chin.199814159
https://doi.org/10.1002/chin.199814159
Publikováno v:
ChemInform. 29
A catalytic ene-like reaction of aldehydes with those vinyl ethers that display the oxygen functionality at the central carbon of an allylic system, e.g., 2-methoxypropene, is discussed in detail. The reaction is promoted by 0.05 equiv. of the 1:1 co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e1d0029d60c12ebc11a1da5b525ebb65
https://doi.org/10.1002/chin.199812261
https://doi.org/10.1002/chin.199812261
ChemInform Abstract: Furan-Terminated N-Acyliminium Ion Initiated Cyclizations in Alkaloid Synthesis
Autor:
Steven P. Tanis, Mark A. Collins, Lisa A. Dixon, Mark C. McMills, Jeffrey W. Raggon, Melissa V. Deaton
Publikováno v:
ChemInform. 30
A study of the utility of furan-terminated N-acyliminium ion initiated cyclizations for the synthesis of linearly fused alkaloid precursors (Figure 2) is presented. The outcome of the cyclization event depends on the position of furan tether attachme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a5f4fac8c9afad34e46b4f84567e779d
https://doi.org/10.1002/chin.199910151
https://doi.org/10.1002/chin.199910151