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101.
A novel synthetic method was developed for the preparation of indole-based conjugated derivatives with satisfied yields. By applying this strategy, a series of new compounds were prepared conveniently. All the obtained new indole derivatives were characterized by spectroscopic analyses, giving satisfactory data corresponding to their expected molecular structures. 相似文献
102.
Eiko Yasui 《Tetrahedron letters》2006,47(5):743-746
A novel method for synthesizing arylhydrazones, the precursor for Fischer indole synthesis, using aryllithium reagents and α-diazo esters that are easily obtained from α-amino acid esters, is described. 相似文献
103.
104.
A.Vijender ReddyK. Ravinder T.Venkateshwar GoudP. Krishnaiah T.V. RajuY. Venkateswarlu 《Tetrahedron letters》2003,44(33):6257-6260
Reaction of indoles with electron deficient olefins under the influence of bismuth triflate has been studied at ambient temperature and affords the corresponding 3-alkylated indoles in excellent yields. 相似文献
105.
Indole alkaloids from the African Strychnos species, their antiplasmodial and cytotoxic action, and structure -activity relationships are discussed in the review 相似文献
106.
Two new monoterpenoid indole alkaloids, tabervarines A (1) and B (2), along with seven known monoterpenoid indole alkaloids, were isolated from the methanol extract of the twigs and leaves of Tabernaemontana divaricata. The structures including the absolute configurations of the new alkaloids were elucidated based on MS, NMR, and ECD calculation. The in vitro cytotoxic activities of the isolated alkaloids against several human cancer cell lines were also evaluated. 相似文献
107.
Zhaohong Lu Ming Yang Pengxi Chen Xiaochun Xiong Prof. Dr. Ang Li 《Angewandte Chemie (International ed. in English)》2014,53(50):13840-13844
A unified and bioinspired oxidative cyclization strategy was used in the first total syntheses of naturally occurring 12‐epi‐hapalindole Q isonitrile, hapalonamide H, deschloro 12‐epi‐fischerindole I nitrile, and deschloro 12‐epi‐fischerindole W nitrile, as well as the structural revision of the latter. Hapalindoles H and Q were also synthesized. 相似文献
108.
Dirhodium(II) Carboxylate Catalyzed Formation of 1,2,3‐Trisubstituted Indoles from Styryl Azides 下载免费PDF全文
Crystalann Jones Quyen Nguyen Prof. Dr. Tom G. Driver 《Angewandte Chemie (International ed. in English)》2014,53(3):785-788
Dirhodium(II)‐carboxylate complexes were discovered to promote the selective migration of acyl groups in trisubstituted styryl azides to form 1,2,3‐trisubstituted indoles. The styryl azides are readily available in three steps from cyclobutanone and 2‐iodoaniline. 相似文献
109.
TEMPO/CuI was found to be an effective catalyst for the cross-coupling of indoles with benzylic amines affording the corresponding bis(indolyl)phenylmethanes under air atmosphere at room temperature in good to excellent yields. The efficiency, easy workup, simplicity, and chemoselectivity of this protocol provide a green and low-cost procedure for the synthesis of these compounds. 相似文献
110.