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1.
J Leitich 《Tetrahedron letters》1980,21(32):3025-3028
The relative rates of formation of and [2+2]cycloadducts of benzyne to , - and , -1,5-cyclooctadiene, - and -cyclooctene are discussed and properties of the adducts (e.g., their unusual hydrogenation) are described. 相似文献
2.
Methods are described for the stereospecific conversion of hydrindenone 3 either to the corresponding fused or fused hydrindanone (1 or 2, respectively.) 相似文献
3.
Intramolecular DIELS-ALDER reactions of requisite trienes led to -1-decalones, an endo intermediate state. 相似文献
4.
The 1H and 13C nmr spectra of , -9-oxobicyclo[3.3.1]nonane-2,4-dicarboxylic acid, 3, in DMSO-d6 or alkaline D2O, clearly show that it exists in a --conformation with carboxyl groups, thus being the first case of - preference of a bicyclo[3.3.1] nonan-9-one due to the presence of ,-2,4- substituents. 相似文献
5.
The 6-hydroperoxy-1,4-cyclooctadiene (), which is formed in the photosensitized oxygenation of 1,5-cyclooctadiene (), affords on further singlet oxygenation 5,8-dihydroperoxy-1,3-cyclooctadiene (), which via triphenylphosphine reduction leads to -5,8-dihydroxy-1,3-cyclooctadiene () and subsequent pyridinium chlorochromate oxidation to 1,3-cyclooctadien-5,8-dione (). 相似文献
6.
N-Acyl derivatives of ,-acosamine and ,-ristosamine were synthesized with high stereo selectivity utilizing intramolecular Michael addition of γ- and δ-carbomoyloxy-α,β-unsaturated esters. 相似文献
7.
P. Caramella F.Marinone Albini D. Vitali Nelson G. Rondan Yun-Dong Wu Timothy R. Schwartz K.N. Houk 《Tetrahedron letters》1984,25(18):1875-1878
Benzonitrile oxide cycloadds preferentially to the substituents of -3,5-di-X-cyclopentenes, where X = OMe, OAc, OCOPh, Br, Cl, and OH. Higher stereoselectivities are found for -2,5-di-X-2,5-dihydrofurans. The origins of these selectivities, and contrasts with acyclic and cyclobutene analogs, are described. 相似文献
8.
1,3,7,9,11,12,14-Heptazapentacene-2,4,8,10 (14,3,9,12)-tetraones (mixed flavins) were prepared by the cyclization of 1,5-dihydro-8-[N-alkyl-N-(5-nitrouracil-6-yl)-amino-5-deazaflavins with Vilsmeier reagent. The mixed flavins oxidized alcohol under neutral condition in sunlight and a remarkable autorecycling was observed. 相似文献
9.
Roshantha A.S. Chandraratna Robert R. Birge William H. Okamura 《Tetrahedron letters》1984,25(10):1007-1010
The electronic absorption spectra of the four new 12---locked retinals (1a–1d) bearing 7-, 11- double bond geometries are described and compared with those of analogous 7-, 11--geometries (1e–1h) and parent retinals (2a-h). 相似文献
10.
Claudio Fuganti Piero Grasselli Stefano Servi Carlo Zirotti 《Tetrahedron letters》1982,23(41):4269-4272
The C4erythro and threo diols (7) and (8) are converted either into the chiral epoxides (13) and (15) or into the enantiomers (14) and (16); the epoxide (13) is used as chiral synthon for the preparation of (3,4) 4-methyl-3-heptanol (21). 相似文献
11.
For 12-- locked retinal analogues, thermal equilibria are established between 11-, 13--1c and 13--2c and between 9-, 11-, 13--1d and 9-, 13--2d; a photoisomerization occurs to transform 2c to --2a and 2d to 9--2b 相似文献
12.
A stereospecific route to -2,2-dimethyl-3-alkenyl-cyclopropanecarboxylic Acids is illustrated by a total synthesis of (±)--Chrysanthemic Acid (11). The key step consists of an alicyclic Claisen rearrangement of -silyl enolates derived from appropriately substituted ()-4-hexen-6-olides [e.g.(9)]. 相似文献
13.
(1,5)-(-)-Karahana ether (8,8-dimethyl-2-methylene-6-oxabi-cyclo[ 3.2.1]octane) and (1,5)-(-)-karahana lactone (8,8-dimethyl-2-methylene-6-oxabicyclo [3.2.1]octan-7-one) were synthesized from ()-3-hydroxy-2,2-dimethylcyclo-hexanone. The natural karahana lactone was shown to be almost racemic (. 1.3 % e.e.). 相似文献
14.
Complexes of the type L2PdCl2 (L = CH3,CN, CH3CH2CN, PhCN) in benzene or chloroform act as homogeneous catalysts in the room temperature to isomerization of ethylchrysanthemate and chrysanthemic acid. 相似文献
15.
Tadashi Nakata Shigeto Nagao Sachiko Takao Tadasu Tanaka Takeshi Oishi 《Tetrahedron letters》1985,26(1):73-74
(1,3,5)-1,3-Dimethyl]-2,9-dioxabicyclo[3.3.1]nonane has been stereoselectively synthesized based on a highly stereoselective method for the synthesis of 1,3--polyol. 相似文献
16.
Tomas Fex 《Tetrahedron letters》1981,22(28):2703-2706
The structures of cytochalasin K, L and M, isolated from the fungus , have been determined by spectroscopic methods, primarily 1H NMR and 13C NMR. 相似文献
17.
Two steroids, 3-oxo-chol-4-ene-24-oic acid () andi ts unsaturated analog have been isolated from the dorid nudibranch , and the acid has been shown to have antifeedant properties. 相似文献
18.
The ∠ equilibrium of the cations of benzo hydroxamic acids, in mineral acid, was studied utilizing 1H NMR spectroscopy, NOEDS and MNDO claculations 相似文献
19.
Sterepolide and dihydrosterepolide, new sesquiterpenes isolated from the fungus , are assigned structures and , respectively. The assignments are based mainly on spectroscopic studies and similarities to isolactarorufin (). A possible mode of biogenesis of these isolactarane type sesquiterpenes is discussed. 相似文献
20.
A new synthesis of (±), (+)- and (-)-lineatin (3,3,7-trimethyl-2, 9-dioxatricyclo [3.3.1.04,7] nonane, ) was achieved. The stereochemistry of (+)-lineatin was established as 1, 4, 5, 7 by an X-ray crystallographic analysis of an intermediate . 相似文献