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1 ate by changing the plaquette topology to an open chain.
2 d chain and the collinear arrangement in odd-open chains.
3       The low-energy structures for the full open chain 58-72 peptide were then computed and were all
4                        Structurally flexible open-chain activated olefins lack the organizational pre
5                                              Open chain aldehydes generated in nucleic acids due to s
6 he Hsp90 inhibitory activity of radamide, an open chain amide chimera of geldanamycin and radicicol.
7                                    While the open-chain amidoxime functionalities do not bind V, the
8 (K*i(1/4)9 pM, third-generation) contains an open-chain amino alcohol cation with two asymmetric carb
9 eptide was threefold greater than that of an open-chain analog, and the cyclic conformation was requi
10  stereoselectivity to those obtained with an open-chain analogue indicated that the ring system does
11 15 that of inactivation by the corresponding open-chain analogue, 4-amino-5-fluoropentanoic acid (3a)
12 reorganized for Cu(II) coordination than its open-chain analogue, with an unusual additional stabiliz
13  although not as potent as the corresponding open-chain analogues.
14                                 Results from open chain and cyclic head groups show that, as expected
15 hlorophosphines, providing approaches to new open-chain and cyclic catena-phosphorus frameworks.
16 e identified MAGEs as a set of isomers, with open-chain and cyclic structures, of the fructosamine mo
17                   For aldotetroses, both the open-chain and furanose forms are considered.
18 ctivation of the receptors, Ala-substituted, open-chain, and truncated analogues were synthesized and
19               This suggests that, unlike the open-chain anlogue, the conformationally rigid analogue
20                                 A knot in an open chain (as distinct from a closed circle) is not rig
21                   Examination of a series of open-chain bis-alkenylamide containing peptides, prepare
22 in is thermodynamically far less stable than open-chain but-2-ene-1,3-dione.
23 nitial cyclization product generated from an open-chain C(7) precursor, D-sedoheptulose 7-phosphate (
24                   Neither thiocarbonates nor open chain carbonates served as substrate nor did a vari
25 the corresponding multiple beta-C-H arylated open-chain carboxamides (anti beta-acyloxy amides).
26  the formation of multiple beta-C-H arylated open-chain carboxamides from the Pd-catalyzed, bidentate
27 five- and six-membered ring compounds and in open-chain compounds the torsion angles vary considerabl
28  proportion of the oligoperoxides formed are open-chain compounds with end groups that suggest that c
29 icated that the phosphosugar is bound in the open-chain configuration.
30 enhanced approximately 5-fold relative to an open-chain congener.
31 opeptidic molecules (one macrocyclic and one open chain) containing an acridine unit have been prepar
32 ffinity and bio-availability compared to its open-chain counterpart.
33 served in the DAG lactone as compared to its open chain DAG counterpart.
34 ole 7 and subsequent macrocyclization of the open-chain derivatives 22-24 using HATU.
35 d temperatures were previously necessary for open-chain diene conjugation, additive-free HDA cycloadd
36 al structure with two azetidine rings and an open-chain diimide moiety.
37 2]annulene by insertion of acetylene into an open-chain diiodo precursor under Sonogashira coupling c
38 ompared with (90)Y-hLL2 agents prepared with open-chain DTPA-type chelating agents.
39                                    After the open-chain energy minima of the 65-72 peptide were gener
40     In the course of generating a library of open-chain epothilones, we discovered a new class of sma
41 tones often deviate in reactivity from their open-chain ester analogues as demonstrated by the CH aci
42 ed in comparison to the reactions of related open-chain esters.
43 rface, is 12.8 kcal/mol less stable than the open chain fluorobutyl cation 3.
44 a cis-enediol(ate) intermediate to yield the open chain form of the product.
45 e enzyme catalyzes ring opening to yield the open chain form of the substrate.
46 ma-OH-1,N(2)-propano-2'-deoxyguanosine to an open chain form, a structure that facilitates pairing wi
47 ormation depended on the concentration of an open-chain form of the sugar in the solution.
48 er one exists in solution exclusively in the open-chain form.
49                     The binding site for the open chain glucitol residue extends to a subsite that is
50 s evoked patterns similar to those evoked by open-chained hydrocarbon odorants, a set of bicyclic com
51 ashion involving the initial formation of an open-chain imidoyl azide intermediate.
52 ion(s) in which the two reactive ends of the open-chain intermediate are located at short distances f
53 ivating the nitrile moiety and leading to an open-chain intermediate that subsequently cyclizes to pr
54 e with isoprene, which proceed stepwise with open chain intermediates, can account for the high regio
55 o exists in solution in equilibrium with its open-chain isomer 2-phenyl-2-(propan-2-ylidenehydrazono)
56  actual ring-opening reaction leading to the open-chain isomer.
57                                          Two open-chain isomers, butadiynylthiol (8) and diethynyl su
58 icylaldehyde and p-tolualdehyde leads to the open-chain isomers, namely (2-hydroxybenzylidene)hydrazo
59                     Syntheses of high-valent open-chain metallostannylene hydride complexes from tran
60                                              Open-chain N-Cbz-protected-peptidoyl benzotriazolides ar
61                               Axially chiral open-chain olefins represent an underexplored class of c
62                        The respective linear open-chain oligomer L-b-B3N3 was also synthesized for co
63                      Relative amounts of the open-chain oligomers so-formed suggest that undried buty
64 ed out in undried butyl acetate yield mainly open-chain oligoperoxides, confirming that propagating c
65                              The reaction of open-chain or cyclic alpha-diketones with specific omega
66 e unbound host that helps to preorganize the open-chained peptide system.
67                     These relatively simple, open-chained peptide systems interact with both chloride
68 nt receptors for six monosaccharides and two open-chain polyols in water at physiological pH.
69 nterconversion between a pentathiepin and an open-chain polysulfur ion intermediate from which a key
70 likely from the unimolecular collapse of the open-chain polysulfur ion.
71 ng an appropriate folded conformation of the open-chain precursor and reducing the energy barrier for
72 ternal template assisting the folding of the open-chain precursor in a proper conformation.
73 ynthesized via the oxidative coupling of two open chain precursors and fully characterized by means o
74 fect on the conformational equilibria of the open-chain precursors is very important.
75  selective for H(2)PO(4)(-) than the related open chain receptor.
76 ed C-H amination was examined with 18 chiral open-chain substrates, which bear a benzylic methylene g
77 nd on the alkaline side, ring closure of the open-chain sugar limits the rate.
78 hiral dipolarophiles (maleates) with chiral, open-chain sugar-derived azomethine ylides yielded enant
79 e of cyclic hemiketal diastereomers, with an open-chain tautomer as a minor component.
80  solution, followed by the 4-hydroxycoumarin open-chain tautomer.
81  mild conditions, a range of both cyclic and open chain tertiary amines was tested as substrates, res
82 es the cysteine at position 198 to ligate an open chain tetrapyrrole covalently in a manner analogous
83 st of apoproteins covalently associated with open-chain tetrapyrrole chromophores.
84 version of ClFe(III)(meso-NH(2)-OEP) into an open-chain tetrapyrrole complex in which the original am
85                                         This open-chain tetrapyrrole complex itself is sensitive to a
86 gnaling, phytochromes need to associate with open-chain tetrapyrrole molecules as the chromophore.
87                           Interestingly, the open-chain tetrapyrrole substrate DHBV is bound in an un
88 me-like photosensory kinase possibly binding open-chain tetrapyrroles.
89 m nearly 0 degrees to 180 degrees and of the open chain tetrasilane Si(4)Me(10) (6) shows a clear con
90 ribe a computer algorithm to detect knots in open chains that is not sensitive to viewpoint and that
91                                The use of an open-chain thiohydantoin derivative also enables the pot
92 t of the dibasic N-terminal Lys of TP in the open-chain TP and its retroisomer was observed in certai
93 Oxone/base oxidations also generate a unique open chain tripyrrin derived from the degradation of a p
94 canonical-type strigolactones but feature an open-chain unit linking structurally diverse A-ring moie
95 el at different positions in three synthetic open-chain variants of a natural trypsin inhibitor MCoTI
96                     It does this by reducing open chain xylose to xylitol, which is reoxidized to xyl