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1 hat nicotinamide and solvent compete for the imidate.
2 xazoline predominantly forms from anti-Z-bis-imidates.
3 Overman's [3,3]-sigmatropic rearrangement of imidates.
4 reaction between cyclopentanol 12 and chiral imidate 30 which was catalyzed by HBF(4) to initially gi
6 g the formation of the C2-sulfonium glycosyl imidate 39 as well as oxazoline 37 as key intermediates
7 te 5 and a subsequent coupling reaction with imidate 6 to produce disaccharide 7, which after deacety
8 w of sulfur imidation methods, classified by imidating agents and compounds with a related behaviour.
11 selective protection/deprotection protocols, imidate and n-pentenyl glycosylations, and functional gr
12 osidation are investigated with thiopyridyl, imidate, and thiotolyl donors as well as differently cro
14 enyl)imidoyl chlorides and the corresponding imidates are easily prepared and can be utilized as comp
15 s the development of S-benzimidazolyl (SBiz) imidates as versatile building blocks for oligosaccharid
16 on the nature of the amine nucleophile, the imidates can react either as the free-base or the hydroc
17 ctions implied that the isolated amidate and imidate complexes are intermediates in the reactions of
18 alyst system consisting of water-soluble Pd--imidate complexes has been enployed for the Suzuki-Miyau
20 glycosyl bromides and activation of the OFox imidates could be conducted in a regenerative fashion.
21 alogs (via in situ conversion of alcohols to imidates, directed C-H amination, and hydrolysis to NH2)
27 nd radical scavengers, we propose that boron-imidates form under the basic reaction conditions that a
29 ng existing methods for converting amides to imidates gave inconsistent or irreproducible results, so
31 ore, mechanistic studies illustrate that the imidate group adjacent to the benzylic position plays cr
32 selectively activating the C(2)-benzylidene imidate group in the presence of the anomeric sulfide gr
35 single flask protocol with formation of the imidate in situ is demonstrated, providing a convenient
36 nyl)benzamides affords high yields of cyclic imidates, instead of the previously reported isoindolin-
37 action mechanism and the modes by which SBiz imidates interact with various promoters of glycosylatio
38 lation of an amide to form the corresponding imidate is a common synthetic problem, often resulting i
40 lladium complex coordinates to both the C(1)-imidate nitrogen and C(2)-oxygen of the trichloroacetimi
41 a novel mechanism in which chelation of the imidate nitrogen to form a cationic palladium(II) interm
42 ocycles were typically prepared by either an imidate or a Weinreb amide route (Schemes 1 and 2), the
43 ected in situ to provide derivatives (methyl imidates or N,N-dimethylamidines) that were amenable to
44 Dibenziodolium hydrogen sulfate, bis(triflyl)imidate, or triflate can be readily converted to various
47 nes presented herein enable direct access to imidate radicals, allowing their first use for H atom ab
49 lylic amines via Overman's [3,3]-sigmatropic imidate rearrangement, and subsequent one-pot deprotecti
52 n peptide settings possible, we developed an imidate salt protecting strategy that employs methyl tri
57 mide, via intermediacy of a sensitive methyl imidate, to the N-acyl aminal reminiscent of psymberin.
62 rmation is achieved starting from anti-E-bis-imidates while trans-oxazoline predominantly forms from
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