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1.
A relatively brief total synthesis of (±)-Faranal [3,4), (6,1O)-3,4,7, 11-tetramethyl-6,10-tridecadien-l-al] (1) is reported. 相似文献
2.
Lithiation of both ()- and ()-3-trimethylsilyl-2-propenyl ,-diisopropyl carbamate 2 affords the (2) -lithium compound 3. Aluminium- or titanium-mediated addition to aldehydes, 4 gives (1)-(3*4*)-enol carbamates 7. A stereospecific Peterson elimination (borontriflouride- or base-mediated) introduces the second double bond either with (3)- or with (3)-configuration. So just by reagent selection for each of the two steps, (1,3)-, (1,3)-, (1,3)-, or (1,3)- dienes 8 - 11, respectively, are prepared with stereoselectivities up to > 99.7% 相似文献
3.
Reaction of mucochloric and mucobromic acid with (ethoxycarbonylmethylene) triphenyl-phosphorane affords the ethyl ester of (2, 4 -4,5-dichloro- and (2, 4) -4, 5-dibromo-2,4-pentadienoic acid respectively; in the latter case ethyl (2 -5-bromo-2-penten-4-ynoate is formed concomittantly. 相似文献
4.
Reaction of (2,3)-2,3-(cyclohexylidenedioxy)butanenitrile, derived from ethyl ()-lactate, with the magnesium enolate of t-butyl acetate gave the corresponding ()-β-amino acrylate derivative, which was transformed into N-benzoyl acosamine by acetylation, stereoselective hydrogenation, acidic hydrolysis, and ring-formation followed by reduction with diisobutylaluminium hydride. 相似文献
5.
Lindlar hydrogenation of substituted methyl (,)-deca-7,9-dien-2-ynoates and substituted methyl (,)-undeca-8,10-dien-2-ynoates affords selectively the corresponding (,,)-trienes. 相似文献
6.
7.
A route towards I-oxygenated eudesmanolides, via a (2+2) photocycloaddition reaction for constructing the decalin framework is described. The following natural substances have been synthesized. (=)-dihydroreynosin (), (±)-1- oxo-dihydronmagnolialide (), (±)-maritimin (), (±)-dihydromagnolialide (), (±)-magnolialide (), (±)-dihydrosantamarine (). Also a synthesis of (±)--santonin () is presented. 相似文献
8.
Titanium(IV) chloride-mediated reaction of 4,5-dihydro-2-(trimethylsiloxy)-3-(trimethylsilyl)furan (1a) with acetaldehyde gave (3S*, 1′R*)-4,5-dihydro-3-(1′hydroxyethyl)-3-(trimethylsilyl)-2(3)furanone (2a), which afforded selectively either (Z)- or (E)-α-ethylidene-γ-butyrolactone (3a) under proper conditions. Facile isomerization of 2a into (3S*, 1′R*)-4,5-dihydro-3-&{1′-(trimethylsiloxy)ethyl}-2(3)furanone (4) suggests an intriguing stereochemical outcome from 2a to (E)-3a via an enolate of 4. 相似文献
9.
Allylic oxidation of 6--(3,3-dimethylallyl)adenosine gave () zeatine riboside , which was isomerized to the () isomer by u.v. irradiation. A method for the regiospecific 3′--succinoylation of these nucleosides is given. 相似文献
10.
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
11.
Both()- and ()-zirconium enolates have been shown to undergo selective kinetic aldol condensation to give mainly -β-hydroxy ketones, esters and amides. 相似文献
12.
Pyrolysis of homoadamant-3-ene (), generated from 1-adamantylcarbene (), leads to the same three olefins (, , and ) that are produced from pyrolysis of 3-homoadamantyl acetate (). 相似文献
13.
Isao Kitagawa Hirotaka Shibuya Hiromichi Fujioka Yoshio Yamamoto Akiharu Kajiwara Kunihiro Kitamura Ayako Miyao Toshio Hakoshima Ken-ichi Tomita 《Tetrahedron letters》1980,21(20):1963-1966
Acid treatment of (IR, 3S,1′S)-1-(1′,2′-Epoxyethyl)-1,2,2-trimethyl-3-acetoxymethyl-cyclopentane ) has been shown to yield three products (, , ), among which and are 1-oxa-bicyclo[3.3.0]octane derivatives formed successive methyl migrations followed by an oxorane ring closure. 相似文献
14.
The biomimetic reactions of epoxygermacrene-D () with basic alumina afforded three new interesting compounds (, , and ), two of which ( and ) have the same carbon skeleton as that of periplanone-A (), a sexual stimulant for the American cockroach. The remaining one () is a bicyclo[3.1.0]hexane derivative, from whch an axisonitrile-3 type compound () has been produced. Finally, preisocalamendiol () was also converted into . 相似文献
15.
J.L. Breton F. Camps J. Coll L. Eguren J.A. Gavin A.G. Gonzalez X. Martorell C. Miravitlles E. Molins J. Torramilans 《Tetrahedron》1985,41(15):3141-3146
A new heliangolide has been isolated from aerial parts of , and identified as (6,10)(3,3a,4,lla)-3a,5,8,11a--tetrahydro-4-acetoxy-3,6, 1O-trimethyl-2,9 (3, 4) -cyclodeca[b] furandione. The structural elucidation of the new compound, named heliangolidin, was carried out by spectral means (MS, IR, 1H and 13C NMR, and two dimensional 1H-13C chemical shift correlations) and X-ray diffraction analysis. 相似文献
16.
Reaction of the cyclic 1, 3-dicarboxylic acid derivatives (), () and () with (R)- or (S)-citronellal (/) gives the enantiomeric tricyclic dihydropyrans (), (), () and (), probably via a 100% stereocontrolled intramolecular cycloaddition. 相似文献
17.
T. Tanaka N. Okamura K. Bannai A. Hazato S. Sugiura K. Manabe S. Kurozumi 《Tetrahedron letters》1985,26(45):5575-5578
(5)-Prostaglandin E2 methyl ester was synthesized from ()-4--butyldimethylsiloxy-2-cyclopentenone by 2-alkenyloxycarbonylation of the organocopper conjugate-addition adduct followed by intramolecular palladium-catalyzed decarboxylative 2-alkenylation. A ()-2-butenylated cyclopentanone derivative was obtained from either 2-[()- or ()-2-butenyloxy-carbonyl]cyclopentanone derivative under the similar reaction condition. 相似文献
18.
Giovanni Fronza Claudio Fuganti Piero Grasselli Giulio Marinoni 《Tetrahedron letters》1979,20(40):3883-3886
The enantiomeric alcohols () and (), obtained from (2,3) tartaric acid and, respectively, -threonine, have been used to construct the C6, enantiomeric deoxy amino sugar derivatives () and () 相似文献
19.
Kinetic stereoselectivities are reported for the micelle-catalyzed basic esterolyses of the four diastereomeric ,-( or )-Phe-( or )-Phe-()-Pro -nitrophenyl esters. 相似文献
20.
A range of conjugated ,-dienes have been prepared in a stereo-specific manner acetylene carbocupration: the value of this procedure has been illustrated by an extremely short synthesis of hexadeca-11, 13-dienal a principle component of Navel Orangeworm Pheromone. 相似文献