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排序方式: 共有155条查询结果,搜索用时 109 毫秒
1.
Joji Ohshita 《Journal of organometallic chemistry》2007,692(16):3526-3531
Palladium-catalyzed synthesis of poly(bromoalkoxymethyl- and bromoalkanoyloxymethylsiloxane)s from poly(hydromethylsiloxane)s was studied. Treatment of poly(hydromethylsiloxane)s with mixtures of allyl bromide and cyclic ethers in the presence of a catalytic amount of PdCl2 gave the corresponding poly[(bromoalkoxy)methylsiloxane]s in good yield. A similar reaction with γ-butyrolactone produced poly[(bromobutanoyloxy)methylsiloxane], although the polymer was highly moisture-sensitive and could not be separated from the reaction mixture. Transformation of the bromoalkoxy unit in the resulting siloxane polymer into an aminoalkoxy group was also examined. 相似文献
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Weiguo Zhang Junyu Xu Jing Cao Chao Fang Jindong Zhu Tao Lu Ding Du 《Tetrahedron》2017,73(23):3249-3254
An in situ activation of isatin-derived α,β-unsaturated acids 2 for the generation of isatin-derived α,β-unsaturated acyl azoliums II was described. The acyl azoliums II were successfully applied to undergo a formal [3 + 3] annulation with 1,3-dicarbonyl compounds to access functionalized 3,4′-spirooxindole δ-lactones 4. A scale-up synthesis and an enantioselective variant of this protocol were also investigated. The stable and easily prepared acids 2 may be further utilized as promising versatile electrophilic 1,3-synthons for divergent synthesis of spirooxindoles. 相似文献
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Mitsuru Kitamura Kenji KuboShogo Yoshinaga Hiroki MatsuzakiKantaro Ezaki Taisuke MatsuuraDaigo Matsuura Noriyuki FukuzumiKeiichiro Araki Masafumi Narasaki 《Tetrahedron letters》2014
A synthetic study of kosinostatin aglycone is reported. Synthesis of key intermediate lactone 3, which corresponds to the BCDE ring fragment, was accomplished, and the precursor BCD ring fragment 5 was synthesized via two routes. First, 5 was synthesized from 2,5-dimethoxybenzaldehyde 16 by the combination of typical known transformations including efficient application of non-aqueous OsO4 oxidation in the presence of PhB(OH)2. However the synthesis required 15 long steps, and its main difficulty was ortho-alkoxycarbonylmethylation of 1-naphthol. Next we attempted to apply our recently developed alkoxycarbonylmethylation of diazonaphthoquinone for the synthesis of 5, and 5 was successfully synthesized in 9 steps from the same starting compound 16. Finally, 5 was stereoselectively converted to lactone 3 via trifluoroacetic acid-mediated cyclization of the 3,4-epoxycylohexanecarboxylic acid derivative. 相似文献
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Laetitia Souillart Nicolai Cramer 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2014,126(36):9794-9798
The lactone motif is ubiquitous in natural products and pharmaceuticals. The Tishchenko disproportionation of two aldehydes, a carbonyl hydroacylation, is an efficient and atom‐economic access to lactones. However, these reaction types are limited to the transfer of a hydride to the accepting carbonyl group. The transfer of alkyl groups enabling the formation of C C bonds during the ester formation would be of significant interest. Reported herein is such asymmetric carbonyl carboacylation of aldehydes and ketones, thus affording complex bicyclic lactones in excellent enantioselectivities. The rhodium(I)‐catalyzed transformation is induced by an enantiotopic C C bond activation of a cyclobutanone and the formed rhodacyclic intermediate reacts with aldehyde or ketone groups to give highly functionalized lactones. 相似文献
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Construction of 6/7 fused bicycles featuring C/D rings of micrandilactone C and rubrifloradilactone B is reported through IMDA reaction of properly designed substrates. Also a route to the construction of a tricycle having A/B ring of nortriterpenoids of schisandra family is reported using RCM and a bromonium ion initiated cycloetherification reaction as the key steps. 相似文献
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A short enantioselective synthesis of (+)-L-733,060 via Shi epoxidation of a homoallylic carboxylate
Lourdusamy Emmanuvel 《Tetrahedron letters》2008,49(40):5736-5738
A short and efficient enantioselective synthesis of (+)-L-733,060 in 92% ee via Shi epoxidation of a homoallylic carboxylate is described. Johnson-Claisen rearrangement was employed to obtain the required carbon backbone, whilst intramolecular reductive O-to-N-ring expansion of a δ-azidolactone was used in the construction of the piperidine moiety. 相似文献
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