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1 lyst loading ((Q)FOX = di-2-quinolinyl-fused-oxazolidine).
2 e nucleophilic reagent to the oxygen atom of oxazolidine.
3 lidine, a monomeric doxorubicin formaldehyde-oxazolidine.
4 ic form with synchronous ring opening of the oxazolidine.
5 yde and epirubicin, which cannot form stable oxazolidines.
6  in the presence of iron salts to afford 1,3-oxazolidines.
7 ion of PhS(O)H, providing conjugated dienone oxazolidine 13.
8 ne in acetic acid produced 5,5-disubstituted oxazolidine-2,4-diones with the formation of a C-O bond
9  the addition of diverse nucleophiles to the oxazolidine-2-one moiety accompanied by the release of c
10 the Diels-Alder reaction of N-2-alkenoyl-1,3-oxazolidine-2-one with cyclopentadiene.
11 y, the starting racemic material, adamantane-oxazolidine-2-one, was resolved into single enantiomers
12 eterocycles by decarboxylation of adamantane-oxazolidine-2-one.
13       Some glucosinolate derivatives such as oxazolidine-2-thione from progoitrin in brassica oilseed
14 f a Crimmins titanium tetrachloride-mediated oxazolidine-2-thione-guided asymmetric glycolate aldol a
15 wed by desulfonation (Al(Hg)), afforded keto-oxazolidine 20, which bears a (E)-Delta(6) double bond.
16  ring closure metathesis of 2-allyl-N-acroyl oxazolidines, 8.
17 -(13)C]capreomycidine (32) was prepared from oxazolidine aldehyde (18) via 1,1-dimethylethyl (4R,1'S)
18 sis of homopentafluorophenylalanine (6) from oxazolidine aldehyde 1 in 57% overall yield and in > 98%
19 lyzed and ZnI2-promoted in situ formation of oxazolidine, alkynyl zinc, and propargylamine intermedia
20  discussed considering a mechanism involving oxazolidine and iminium ions formed in situ followed by
21        Herein, we leverage the tunability of oxazolidine and oxazolidinone rings to systematically ch
22 route for the construction of functionalized oxazolidines and imidazolidines.
23 drolysis of the primary photoproducts, spiro-oxazolidines and thiazolidines, under mild conditions un
24 ation of pseudoprolines (i.e. serine-derived oxazolidines as another type of protecting group), a com
25      This study reveals that a simple chiral oxazolidine-based carboxylic acid can be readily transfo
26                                     By using oxazolidine-based pseudoprolines (PsiPro) substituted by
27 % overall yields and six to seven steps from oxazolidine beta-methyl ester 4.
28 molecular systems consisting of two indolino-oxazolidine (Box) moieties connected to an aromatic brid
29  on the hydride used for the cleavage of the oxazolidine C-O bond.
30 ienylethene, Z/E isomerization and acid-base oxazolidine change cause selective addressabilities.
31  resolution (CIDR) of trans-Fox (fluorinated oxazolidine) chiral auxiliary is reported.
32 sting of two molecules of the parent drug as oxazolidine derivatives bound together at their 3'-nitro
33 into the target molecules and application of oxazolidine derivatives such as 1-arylethanol-2-amines o
34  results in its conversion to the beta-amino oxazolidine dione observed under conditions used in our
35 lallylcarbonate, leading to the formation of oxazolidine-diones.
36            Acid-mediated deprotection of the oxazolidine, followed by N-acylation and Birch reduction
37  diastereoisomers through an atroposelective oxazolidine formation.
38 also provide evidence that suggests that the oxazolidine forms in situ, since cotreatment with doxoru
39  from a readily available chiral fluorinated oxazolidine (Fox).
40 luoromethylated prolines, pseudoprolines and oxazolidines has been achieved.
41 ymmetric synthesis of spirooxindole embedded oxazolidines has been developed via a domino reaction in
42  from dihydroisobenzofuran, pyrrolidine, and oxazolidine heterocycles can also be used as a substrate
43                              Dithienylethene oxazolidine hybrid system connected through an isomeriza
44              Moreover, an additional step of oxazolidine hydrolysis or ring-opening with hydrogen cya
45 yrenes under these conditions to provide 1,3-oxazolidines in a formal aminohydroxylation of the alken
46 -derived aldehyde 26, respectively, afforded oxazolidine intermediates 27 and 33.
47 control observed during the formation of the oxazolidines is best explained by the stereoelectronic e
48 ed aldehyde 4, followed by hydrolysis of the oxazolidine, liberation of the amino group, and N-acylat
49 e obtained through Katritzky's benzotriazole-oxazolidine methodology, a highly diastereoselective suc
50 from aromatic aldehyde was achieved applying oxazolidine methodology.
51 ty to form cyclic formaldehyde conjugates as oxazolidine moieties and that the cyclic conjugates are
52  caged system, bearing a 1,4-diazepine fused oxazolidine moiety and containing three successive N,O-a
53 burn reaction leading to the formation of an oxazolidine-N-oxyl compound was observed by electron par
54 spectra were observed due to the presence of oxazolidine-N-oxyl derivatives.
55 lease doxazolidine (Doxaz), the formaldehyde-oxazolidine of doxorubicin that cross-links DNA to trigg
56 m as a dimeric formaldehyde conjugate of the oxazolidine of doxorubicin.
57 ons with carbonyl compounds to give bicyclic oxazolidine products in good overall yields.
58                         This process affords oxazolidine products that can be easily manipulated to y
59 mmetric cyclization of an amino acid derived oxazolidine provided a key lactam intermediate 11, which
60 lation is found between the puckering of the oxazolidine ring and the peptide bond conformation.
61 M-2 beta-lactamase retain the carbons of the oxazolidine ring of clavulanate.
62 d-mediated amide cleavage, and acid-mediated oxazolidine ring opening.
63                             On one hand, the oxazolidine ring opening/closure of Box moieties can be
64 oped incorporating an additional substituted oxazolidine ring, and providing improved enantiocontrol
65 BH(4)/CeCl(3) or DIBAL-H), hydrolysis of the oxazolidine ring, liberation of the amino group, and ins
66 her with three methylene groups, two forming oxazolidine rings and one binding the oxazolidines toget
67                   The resulting 2-alkoxy-1,2-oxazolidines showed good enantiopurities, and density fu
68 ectra of 2,4-disubstituted thiazolidines and oxazolidines that cannot be attributed to classical dipo
69 ating it into the ring system of N-carbamoyl oxazolidines, thiazolidines, or imidazolidines.
70 ns and the Pt-catalyzed isomerization of the oxazolidine to an amide under neutral conditions.
71 r cyclization of unsaturated aldehyde via an oxazolidine to prepare C-3-substituted tetrahydroisoquin
72 orming oxazolidine rings and one binding the oxazolidines together at their 3'-amino nitrogens.
73 incorporation of trifluoromethyl substituted oxazolidine-type pseudoprolines (CF3-PsiPro) into peptid
74  to highly functionalized imidazolidines and oxazolidines via S(N)2-type ring-opening of the correspo
75                                 The bicyclic oxazolidines were obtained from chiral N-alkenylamino al
76 ines were formed as the cis-isomers, whereas oxazolidines were produced as trans-isomers exclusively.
77 chemosensor probes PS (thiazolidine) and BO (oxazolidine) were designed and synthesized.
78  (3-methyl and 3-tert-butyl 2,2-diphenyl-1,3-oxazolidine) were synthesized; they had approximately th
79  been further utilized to obtain substituted oxazolidines whenever the epoxide has been reacted with