Zobrazeno 1 - 10
of 459
pro vyhledávání: '"Ernest Wenkert"'
Publikováno v:
CHIMIA, Vol 46, Iss 4 (1992)
Acetoxymaleic anhydride (AMA) has been shown to be a versatile ketene equivalent in the Diels-Alder reaction for the conversion of 1,3-dienes into cyclohexanones. The new transformation has been applied to an alternate synthesis of methyl cis-dihydro
Externí odkaz:
https://doaj.org/article/abebd57947394421bf3da951bc429a87
Publikováno v:
Synthetic Communications. 31:707-710
Diels-Alder reaction of cyclopentadiene and 1,3-cyclohexadiene with propiolic ester 6 under thermal and high pressure conditions gave an epimer mixture of ketoester 8 and 10, subsequently converted into bicyclic ketones 1 and 2.
Autor:
Ornelio Rosati, Ernest Wenkert, Francesco Epifano, Massimo Curini, Yousheng Guan, Maria Carla Marcotullio
Publikováno v:
Helvetica Chimica Acta. 83:755-759
The Kanematsu transformation was employed for the preparation of tetrahydroisobenzofuran-4-carboxylic acid (12), α-methylation, subsequent conversion into the diazoethanone 14, and, finally, treatment with dirhodium tetraacetate of which furnished t
Autor:
Haripada Khatuya, Ernest Wenkert
Publikováno v:
Synthetic Communications. 29:3051-3055
Callosobruchusic acid, a monoterpene dicarboxylic acid, has been prepared in five steps from 2-methylfuran and methyl α-diazopropionate.
Autor:
Ernest Wenkert, Haripada Khatuya
Publikováno v:
Synthetic Communications. 29:2413-2417
A variety of oxidizing agents convert 5-hydroxy-4,5-dihydroisobenzo-furan into phthalaldehyde. Other oxidizing agents produce both phthalaldehyde and its 4-hydroxy derivative.
Autor:
Haripada Khatuya, Ernest Wenkert
Publikováno v:
Tetrahedron Letters. 40:5439-5442
Reactions of various α-alkyl-substituted furans with ethyl diazoacetate or methyl diazopropionate in the presence of Rh2(OAc)4, followed by iodine-induced isomerization, yielded a variety of functionalized 1,3-diacyl-butadienes (furan ring-unravelle
Publikováno v:
Tetrahedron Letters. 40:5171-5174
Reactions of β-methylfuran and 2,4-dimethylfuran with ethyl diazoacetate in the presence of [Rh2(OAc)4] catalyst, followed by iodine-induced isomerization, yielded furan ring-unravelled products. The results are compared with those of α-methylfuran
Autor:
Ernest Wenkert, Haripada Khatuya
Publikováno v:
Helvetica Chimica Acta. 82:511-514
(±-(2E,4E)-2,7-Dimethylocta-2,4-dienedioic acid (1) was synthesized efficiently from furan, employing a rhodium-carbenoid-induced furan-ring-unravelling reaction followed by an unusual NaBH4/CeCl3⋅7 H2O reduction, Wittig-Horner olefination, and di
Autor:
Haripada Khatuya, Ernest Wenkert
Publikováno v:
Helvetica Chimica Acta. 81:2370-2374
Autor:
Song Liu, Ernest Wenkert
Publikováno v:
The Journal of Organic Chemistry. 59:7677-7682