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11.
Subhash P. Chavan Pallavi Sharma R. Sivappa Uttam R. Kalkote 《Tetrahedron letters》2006,47(52):9301-9303
An efficient utilisation of RCM leading to a convenient synthesis of a pentacyclic indole alkaloid is described. 相似文献
12.
Sharpless asymmetric dihydroxylation ligands were synthesized using a triazine spacer group in two, high yielding steps from cheap, readily available starting materials. The ligands, gave good enantioselectivities in the asymmetric dihydroxylation of alkenes and may provide a very economic alternative to current systems. 相似文献
13.
M. Somi Reddy 《Tetrahedron》2007,63(2):331-336
An asymmetric synthesis of substituted piperidines has been described. β-Cyclodextrin- or oxazaborolidine-catalyzed asymmetric reduction of α-azido aryl ketones to the corresponding alcohols has been employed as the key step along with ring closing metathesis and selective dihydroxylation. 相似文献
14.
Sergiy A. Siry 《Tetrahedron letters》2010,51(49):6406-6409
2-Polyfluoroalkylthiopyrylium salts have been synthesized by oxidative aromatization of 2-polyfluoroalkyl-2H-thiopyrans with triphenylmethane tetrafluoroborate. Nucleophilic addition of methanol, sodium azide, or urea to 2-trifluoromethylthiopyrylium tetrafluoroborate in a basic medium proceeds at the α-position to give the corresponding 2-substituted 6-trifluoromethyl-2H-thiopyrans whereas imidazoles, fluorine-containing 1,2,3-triazole, potassium thiolacetate, and sodium nitromethane afford mixtures of 2H- and 4H-thiopyrans. cis-Dihydroxylation of 6-trifluoromethyl-2-methoxy-2H-thiopyran affords the fluorine-containing thiohexenopyranoside derivative 8. 相似文献
15.
The highly stereoselective synthesis of (−)-epi-, (−)-allo- and neo-quercitols as well as stereospecific synthesis of (−)-talo- and (+)-gala-quercitols have been achieved. The general strategy is employing dihydroxylation of the isolated double bond of various kinds of protected chiral (1,4,5)-cyclohex-2-ene-triols, which are derived from d-(−)-quinic acid. The choosing of protecting groups from either BBA (butane 2,3-bisacetal) or acetyl groups will result in the various degrees of stereoselectivity of dihydroxylation. On the other hand, the cyclohexylidene acetal moiety is attributed to the stereospecificity during dihydroxylation to afford the request molecules. 相似文献
16.
Mukund K. Gurjar Yakambram Pedduri C.V. Ramana Vedavati G. Puranik Rajesh G. Gonnade 《Tetrahedron letters》2004,45(2):387-390
Dihydroxylation of the glucose derived α,β-unsaturated lactones 6 and 13 was found to be on the α-face of the pyranolactone ring exclusively. The resulting dihydroxylated compound from 13 has been used in a synthesis of the lactone 4, which corresponds to C(1)-C(11) of peloruside A. 相似文献
17.
Chuanjun Song Shende Jiang * Gurdial Singh . Department of Chemistry University of Sunderland Sunderland SR SD UK . Department of Applied Chemistry Tianjin University Tianjin P. R. China 《高等学校化学研究》2002,18(2):146-152
IntroductionTheshikimatepathwayisanimportantbiosyn theticsequencein plants ,fungiandmicroorganismsfortheconversionofcarbohydratestothearomaticaminoacids (L phenylalanine ,L tyrosineandL tryptophan)andprecursorstothefolatecoenzymes ,alkaloidsandvitamins[1] .As… 相似文献
18.
A key intermediate corresponding to a rare sugar framework has been synthesized, starting from d-xylose, an inexpensive carbohydrate. This approach gave access to new elaborated sugar moieties for structure–activity relationships in the KRN research. 相似文献
19.
Bharathi Balagam 《Tetrahedron letters》2008,49(6):1071-1075
An improved process has been developed for the osmium-catalyzed dihydroxylation of olefins via in situ formation of NMO from NMM using CO2 catalysis and H2O2. All olefins examined were selectively cis-dihydroxylated to their corresponding diols in good to excellent yields, and by the use of chiral ligands, high enantiomeric excesses were obtained. 相似文献
20.
Dasari Ramesh Singanaboina Rajaram Peddikotla Prabhakar Udugu Ramulu Dorigondla Kumar Reddy Yenamandra Venkateswarlu 《Helvetica chimica acta》2011,94(7):1226-1233
A simple asymmetric total synthesis of stagonolide G ( 1 ) is described. Asymmetric dihydroxylation, regioselective epoxide ring opening, and vinyl Grignard reactions are involved in generating the stereogenic centers C(4) and C(8), followed by Grubbs‐II‐catalyzed ring‐closing metathesis (RCM). 相似文献