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Roman Kaiser 《Helvetica chimica acta》1984,67(5):1198-1203
(5 R*,9S*)- and (5R*,9R*)-2,2,9-Trimethyl-1,6-dioxaspiro [4.4]non-3-ene ( 1a and 1b resp.) and their dihydro derivatives 2a and 2b are described as new constituents of geranium oil. The structures and configurations of 1a , 1b , 2a , and 2b , are based on spectra interpretation and syntheses. Also some other monoterpenoid constituents identified in the same boiling range are discussed. 相似文献
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Guliya G. Bizhanova Kyrill Yu. Suponitsky Yulia V. Vakhitova Rail R. Gataullin 《Tetrahedron》2017,73(2):109-115
We synthesized methyl ester of N-(1-methylbut-2-en-1-yl)-N-phenylglycine which underwent acid catalyzed aromatic amino Claisen rearrangement to provide methyl-N-[2-(1-methylbut-2-en-1-yl)phenyl]glycinate. A mixture of syn- and anti-atropisomeric methyl-N-acetyl-N-[4-methyl-2-(1-methylbut-2-en-1-yl)phenyl]glycinates was obtained either by the reaction of this ester with acetyl bromide or by the reaction of the sodium salt of N-acetyl-2-(1-methylbut-2-en-1-yl)-4-methylaniline with methyl bromoacetate. Upon saponification of the synthesized ester mixture the syn-atropisomer of N-acetyl-N-[4-methyl-2-(1-methylbut-2-en-1-yl)phenyl]glycine was isolated by fractional crystallization. Treatment of the obtained acids with acetic anhydride, ethyl chloroformate, dicyclohexylcarbodiimide or isopropenylacetate leads to compounds of 4,5-dihydro-3aH-methano[1,3]oxazolo[3,2-a]quinolin-2-one structure. 相似文献
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Semenov B. B. Smushkevich Yu. I. Grintselev-Knyazev G. V. Antipin M. Yu. 《Russian Chemical Bulletin》2001,50(3):570-571
Russian Chemical Bulletin - 相似文献
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Pezdirc L Bevk D Groselj U Meden A Stanovnik B Svete J 《Journal of combinatorial chemistry》2007,9(4):717-723
Combinatorial solution-phase cycloadditions of (1Z,4R*,5R*)-4-benzoylamino-5-phenylpyrazolidin-3-on-1-azomethine imines 3 to beta-keto esters 4 afforded a library of 26 bicyclic pyrazolidinones 5 in 6-89% yields and in 14-100% de. All products were isolated in >90% purity according to 1H NMR, and 25 of them were analytically pure. The structures of cycloadducts were confirmed by NMR and X-ray diffraction. Most of the products were isolated as mixtures of the major (1S*,2S*,3R*,5R*,6R*)-epimers 5 and the minor (1R*,2S*,3R*,5R*,6R*)-epimers 6. Epimerization of cycloadducts 5/6 at the anomeric position 1 in solution was confirmed by 1H NMR. 相似文献
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A series of cyclic imides bearing a omega-(4-aryl and 4-heteroaryl-1-piperazinyl)alkyl moieties was synthesized and tested in vivo for anxiolytic activity. The in vitro binding affinities of these compounds were also examined for 5-HT1A receptor sites. Structure-activity relationships within these series are discussed. One of these compounds, (1R*,2S*,-3R*,4S*)-N-[4-[4-(2-pyrimidinyl)-1-piperazinyl]butyl]-2,3- bicyclo[2.2.1]heptanedicarboximide (1: tandospirone), was found to be equipotent with buspirone in its anxiolytic activity and more anxio-selective than buspirone and diazepam. Tandospirone (1) is currently undergoing clinical evaluation as a selective anxiolytic agent. 相似文献