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1 plete or partial thermal isomerization via a rearrangement reaction.
2 ted oxyanionic 6-exo-dig cyclization/Claisen rearrangement reaction.
3 ould act as general acid-base catalysts in a rearrangement reaction.
4 s that are converted to imines via a Beckman rearrangement reaction.
5 antly to the lowering of the barrier for the rearrangement reaction.
6 tion but has little effect on the subsequent rearrangement reaction.
7 lsilyl groups for product formation in these rearrangement reactions.
8 f the p-terphenyl systems was susceptible to rearrangement reactions.
9 l insights into how enzymes catalyze complex rearrangement reactions.
10 amolecular Mitsunobu, and tandem epoxidation/rearrangement reactions.
11 -addition reactions, and in some cases, ring rearrangement reactions.
12 strand refolding is a novel mechanism in DNA rearrangement reactions.
13 rsity of 5'-deoxyadenosylcobalamin-dependent rearrangement reactions.
14 es mediate a wide range of important genetic rearrangement reactions.
15 uring the hydrogen atom transfer and radical rearrangement reactions.
16 s facilitating disulphide bond formation and rearrangement reactions.
17 titude of possible intra- and intermolecular rearrangement reactions.
18 nd of the cofactor, leading to radical-based rearrangement reactions.
19 tions and appear to reflect isomerization or rearrangement reactions.
20  and found missed fragmentations in specific rearrangement reactions.
21 asymmetric Pauson-Khand reaction, an Overman rearrangement reaction, a ring-closing metathesis reacti
22 f the route outlined herein include specific rearrangement reactions and a retro-aldol cleavage of ri
23 sound, and that this allows us to accelerate rearrangement reactions and bias reaction pathways to yi
24  evidenced by their formal [1,3]-sigmatropic rearrangement reactions and the rapid additions of oxyge
25 e ratio can be operated such that structural rearrangement reactions and/or CID are achieved as a fun
26       These esters underwent the photo-Fries rearrangement reaction, and the microheterogeneous media
27                                  Carbocation rearrangement reactions are of great significance to syn
28 r Heck alkenylation and radical-based Smiles rearrangement reactions as key steps.
29 ange from ligand release to isomerization or rearrangement reactions at high urea concentrations.
30  boron compounds are readily synthesized via rearrangement reactions between Lewis acidic B(C6F5)3 an
31 lations that predict rate enhancement of the rearrangement reaction by the interaction of the migrati
32 investigation demonstrates that heterocyclic rearrangement reactions can be used to control macrocycl
33  Here we report that the complex cyclization/rearrangement reaction catalyzed by abietadiene synthase
34 evidence for elucidating the carbon backbone rearrangement reaction catalyzed by PylB during the bios
35               Ring hydroxylation and coupled rearrangement reactions catalyzed by 4-hydroxyphenylpyru
36 ficant differences from the desaturation and rearrangement reactions catalyzed by other family member
37  of a cascade click cycloaddition and a ring rearrangement reaction, followed by a reductive step.
38 en atom, thereby retarding the ring cleavage/rearrangement reaction generally encountered with relate
39            A diastereoselective addition and rearrangement reaction has been developed for the synthe
40 ompounds, unexpected stereoelectronic-driven rearrangement reactions have been discovered.
41              Using the halide-induced ligand rearrangement reaction (HILR), a heteroligated Pt(II) tr
42 0'Rxn, were determined for the net reduction/rearrangement reaction, His82-Fe3+-His18 + e- --> Met80-
43                                 The oxy-Cope rearrangement reaction in the antibody AZ28 is investiga
44              MoaA/MoaC catalyze a remarkable rearrangement reaction in which guanosine-5'-triphosphat
45                                              Rearrangement reactions in organic chemistry are attract
46 tions change little during the course of the rearrangement reaction, in contrast to the large conform
47                                The presented rearrangement reaction, in which the presumed N-acylated
48  example of a biocatalytic [2,3]-sigmatropic rearrangement reaction involving allylic sulfides and di
49                                            A rearrangement reaction involving the indole nucleus was
50                                              Rearrangement reactions involving migration of fucose an
51      The results show that the core, radical rearrangement reaction is culled from the catalytic cycl
52 ing the stereochemical outcomes of oxidative rearrangement reactions not easily determined by standar
53    Under these conditions, no strain-induced rearrangement reactions occur, delivering p-phenylene un
54 rithm is able to cope with general molecular rearrangement reactions occurring during EI in GC/MS mea
55  to occur via the facile and reversible F/Ph rearrangement reaction of 1 to cis-[(Ph(3)P)(2)Rh(Ph)(Ph
56                                            A rearrangement reaction of biarylphosphine-supported Pd(I
57 e describe an Al-promoted, Co-mediated O-->C rearrangement reaction of cyclic enol ethers.
58 es is reported through a Lewis acid mediated rearrangement reaction of enol ethers bearing an Co-alky
59 le-catalyzed, trimethylsilyl halide-promoted rearrangement reaction of glycidol acetals to form halog
60       We report the discovery of an aromatic rearrangement reaction of O-(arenesulfonyl)hydroxylamine
61                                      A novel rearrangement reaction of the unconjugated allylic amine
62 formed from the tandem cyclopropanation/Cope rearrangement reaction of vinylcarbenes with dienes.
63                    The base-induced (t-BuOK) rearrangement reactions of 3,4-dihydro-2H-1,2,3-benzothi
64                            Two CuCN-mediated rearrangement reactions of allenylcyclopropanols to cycl
65 ynthetic chemists have been intrigued by the rearrangement reactions of alpha-santonin and santonin-d
66  we report on the limitations of sigmatropic rearrangement reactions of aryl allyl anilines, which de
67                                              Rearrangement reactions of C4-alkoxides on O-covered Mo(
68                    Two base-mediated cascade rearrangement reactions of diallyl ethers were developed
69                            Most of the known rearrangement reactions of donor-acceptor cyclopropanes
70 The mechanisms of the BF3-catalyzed Meinwald rearrangement reactions of five epoxides in dichlorometh
71                                     Yet, the rearrangement reactions of onium ylides via gold catalyz
72         The first computational study of the rearrangement reactions of oxiranes initiated by lithium
73 controlled cyanate-to-isocyanate sigmatropic rearrangement reactions of the corresponding allyl carba
74    This process is followed by acid-promoted rearrangement reactions of the formed homoallenic halohy
75                               Some potential rearrangement reactions of the initial binding products
76 ed by sare1259, catalyzes multiple oxidative rearrangement reactions on 34a-deoxyrifamyin W to yield
77 ochemically complementary to related Claisen rearrangement reactions--processes that typically delive
78 2)-fold slower rate of the substrate radical rearrangement reaction relative to k(obs), and the rever
79 n "short circuit" complex cyclization and/or rearrangement reactions, resulting in the production of
80                   This step is followed by a rearrangement reaction that is rate-limited by an unfold
81               Automerization is defined as a rearrangement reaction that yields a degenerate form of
82 hemical models consistent with each of these rearrangement reactions that account for the formation o
83 a- and beta-thujone can undergo two distinct rearrangement reactions that could, in principle, serve
84 -mediated catalysis of the fragmentation and rearrangement reactions that remain unprecedented among
85 ondary amines, undergo a fascinating thermal rearrangement reaction to afford Z-alpha,beta,gamma,delt
86 owers the propensity for the photo-Favorskii rearrangement reaction to occur and opens the reaction p
87 se subsequently undergo phospha-Claisen type rearrangement reactions to give the respective substitut
88 The sulfonamide 4c predominantly undergoes a rearrangement reaction under acidic and neutral conditio
89 ar structure that undergoes different exotic rearrangement reactions upon photochemical and thermal s
90 ergo the combined C-H functionalization/Cope rearrangement reaction via an s-cis/boat transition stat
91     An enantioselective alkoxylation/Claisen rearrangement reaction was achieved by a strategic desym
92                      Meanwhile, a unique 3,7-rearrangement reaction was identified to furnish an unpr
93 ing materials by Lewis acid induced skeletal rearrangement reactions was studied under stable ion con
94           The mechanism and the scope of the rearrangement reaction were investigated.
95 rmally and photochemically mediated skeletal rearrangement reactions were also recorded.
96 g the course of these studies, several novel rearrangement reactions were encountered while attemptin
97  in a tandem ammonium ylide generation/[2,3]-rearrangement reaction, which formally represents a pall
98 and photolytic cycloaddition/1,5-sigmatropic rearrangement reactions with 11a-d with N(2) retention t
99  different mechanisms are operative in these rearrangement reactions, with the pathway depending on t
100 he conversion of DHHA to PCA, probably via a rearrangement reaction yielding the more reactive 3-oxo