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1 ortance for the synthesis of pure samples in organic chemistry.
2 ntal lineC bonds is a ubiquitous reaction in organic chemistry.
3 molecule remains a fundamental challenge in organic chemistry.
4 same time one of the youngest disciplines of organic chemistry.
5 ies, many of which are legendary in physical organic chemistry.
6 roaches of fullerenes are the holy grail for organic chemistry.
7 rful carbon-carbon-bond-forming reactions in organic chemistry.
8 ution to unaddressed challenges in synthetic organic chemistry.
9 nts an environmentally benign methodology in organic chemistry.
10 ortant in plantery atmospheres and synthetic organic chemistry.
11 alpha and beta silicon effects from physical organic chemistry.
12 olecules, as well as useful intermediates in organic chemistry.
13 ions and the resulting impact on atmospheric organic chemistry.
14 Aromaticity is a key concept in organic chemistry.
15 in fields such as pharmaceutical science and organic chemistry.
16 y to possess richer chemistry than the known organic chemistry.
17 coordination chemistry or as nucleophiles in organic chemistry.
18 r constructing carbon-carbon double bonds in organic chemistry.
19 the beginning of a synergy between WGSR and organic chemistry.
20 a prominent role in both drug discovery and organic chemistry.
21 hus far been achieved only through synthetic organic chemistry.
22 inones are common stoichiometric reagents in organic chemistry.
23 anilines has been a significant challenge in organic chemistry.
24 barring potential applications in synthetic organic chemistry.
25 ual property of a facially polarized ring in organic chemistry.
26 ironmentally benign reduction methodology in organic chemistry.
27 fundamentally important functional groups in organic chemistry.
28 ee) compounds remains a challenge in modern organic chemistry.
29 tereoselectively, are central to research in organic chemistry.
30 to proposed mechanisms based on knowledge of organic chemistry.
31 try and important synthetic intermediates in organic chemistry.
32 lization is a central challenge in synthetic organic chemistry.
33 ve recently gained attention in the field of organic chemistry.
34 development of new and useful strategies in organic chemistry.
35 on reactions is a long-standing challenge in organic chemistry.
36 ins one of the most formidable challenges in organic chemistry.
37 for their synthesis is an important goal in organic chemistry.
38 g reactions remains an unsolved challenge in organic chemistry.
39 arbonyl compounds are key building blocks in organic chemistry.
40 are considered important synthetic tools in organic chemistry.
41 eaction has long been a contentious issue in organic chemistry.
42 mited attention and application in synthetic organic chemistry.
43 as re-emerged as a major target of synthetic organic chemistry.
44 ave become a cornerstone of modern synthetic organic chemistry.
45 versus nonbiological catalysis in synthetic organic chemistry.
46 ined with some of the most heated debates in organic chemistry.
47 of the bond renders it the strongest one in organic chemistry.
48 t versatile of all reactive intermediates in organic chemistry.
49 nion has fundamental importance to synthetic organic chemistry.
50 lecules represents a formidable challenge in organic chemistry.
51 significant transformations in contemporary organic chemistry.
52 is emerging as a powerful tool in synthetic organic chemistry.
53 their use as powerful reagents in synthetic organic chemistry.
54 are versatile building blocks for synthetic organic chemistry.
55 uld find widespread application in synthetic organic chemistry.
56 eaction has long been a contentious issue in organic chemistry.
57 hemical depletion of which furnishes Titan's organic chemistry.
58 ns are employed extensively in many areas of organic chemistry.
59 utes a field of great relevance in synthetic organic chemistry.
60 soon rival and potentially eclipse synthetic organic chemistry.
61 occupy well-established ground in classical organic chemistry.
62 is an entrenched synthetic disconnection in organic chemistry.
63 other water molecules and allows for a rich organic chemistry.
64 ated C-H bond remains a central challenge in organic chemistry.
65 omprehensive way the structural diversity of organic chemistry.
66 er disk and that the disk supports an active organic chemistry.
67 ectrophiles are important transformations in organic chemistry.
68 nucleophile is of fundamental importance in organic chemistry.
69 key factor in shaping the known universe of organic chemistry.
70 ation, much as synthetic approaches informed organic chemistry.
71 seeding newly formed planets with prebiotic organic chemistry.
72 catalysts underpins much of modern synthetic organic chemistry.
73 should become a useful synthon in synthetic organic chemistry.
74 cular interest as a biocatalyst in synthetic organic chemistry.
75 hich are valuable synthetic intermediates in organic chemistry.
76 ereby to one of the fastest growing areas of organic chemistry.
77 tivity still remains a constant challenge in organic chemistry.
78 products is critical for drug discovery and organic chemistry.
79 historically been of interest in theoretical organic chemistry.
80 of efficiency and atom economy in synthetic organic chemistry.
81 s become a fundamental strategy in synthetic organic chemistry.
82 ter use, thus making it a convenient tool in organic chemistry.
83 ns one of the obvious goals in the synthetic organic chemistry.
84 ety of valuable transformations in synthetic organic chemistry.
85 luggish in catching up with modern trends in organic chemistry.
86 le perovskites may bring new breakthrough in organic chemistry.
87 is an altogether new addition to the area of organic chemistry.
88 ation and application of ynones in synthetic organic chemistry.
89 stainable solutions to problems in synthetic organic chemistry.
90 mong the most versatile functional groups in organic chemistry.
91 exploit the capabilities of modern synthetic organic chemistry.
92 d strategically important transformations in organic chemistry.
93 nt ring closure, is an important reaction in organic chemistry.
94 esis as well as the parallels with synthetic organic chemistry.
95 milarities to the Birch reduction known from organic chemistry.
96 ons and is hence a useful tool for synthetic organic chemistry.
97 ortant classes of isomerization reactions in organic chemistry.
98 is one of the archetypal transformations of organic chemistry.
99 ling opens unique opportunities in synthetic organic chemistry.
100 emains a challenge in the field of synthetic organic chemistry.
101 ng the most commonly used switching units in organic chemistry.
102 ive strategies for molecular construction in organic chemistry.
103 oscopy as a standard analytical technique in organic chemistry.
104 s a longstanding and formidable challenge in organic chemistry.
105 rable relevance to biosynthetic reactions in organic chemistry.
106 international membership by promoting modern organic chemistry.
107 servations on the protean nature of physical organic chemistry.
108 cal techniques of molecular-level control in organic chemistry, allow preparation of well-defined pol
109 xtbook example of electrocyclic reactions in organic chemistry and a model for photobiological reacti
110 from the perspective of fundamental physical organic chemistry and aid in understanding their behavio
111 enations constitute fundamental processes in organic chemistry and allow for atom-efficient and clean
112 ast class of extremely versatile reagents in organic chemistry and are particularly useful in the pre
115 ns range from classical protective groups in organic chemistry and cleavable linkers for solid phase
116 lection, and DNA sequencing to combinatorial organic chemistry and compound identification has made e
117 le, provided that the program's knowledge of organic chemistry and data-based artificial intelligence
118 oline-based radiotracers were synthesized by organic chemistry and evaluated in radioligand binding a
121 ts and solutes are a cornerstone of physical organic chemistry and have been the subject of investiga
122 Carbenes are important intermediates in organic chemistry and have been widely applied in variou
123 r compounds have long played a vital role in organic chemistry and in the development of novel chemic
127 N102 demonstrates that, by bringing together organic chemistry and neuroscience, molecular entities c
128 up transformations are applicable in general organic chemistry and not restricted to carbohydrate che
129 e NOS played in the launch of The Journal of Organic Chemistry and Organic Reactions and the initiati
130 ry and structure in the rapid development of organic chemistry and physical organic chemistry over th
131 athesis (CM) reaction is used extensively in organic chemistry and represents a powerful method for t
133 autocatalysis-occupies a unique position in organic chemistry and stands as an eminent challenge for
135 de organic materials, and recent progress in organic chemistry and surface chemistry has led to the s
136 lysed transformations are a powerful tool in organic chemistry and the enormous progress, which has b
139 s defined by Huckel's rule, are key ideas in organic chemistry, and are both exemplified in biphenyle
142 ve played a prominent role in the history of organic chemistry, and they continue to be important as
143 y and selectivity is at the core of physical organic chemistry, and this knowledge can be used to inf
145 to test the scope of heavy-atom tunneling in organic chemistry, and to check the accuracy of one-dime
146 wn to be powerful biocatalysts for synthetic organic chemistry applications and were also suggested t
147 oven their versatility as synthetic tools in organic chemistry, are currently on the rise in fluorina
148 redox catalysis has come to the forefront in organic chemistry as a powerful strategy for the activat
149 enzymic reactions, and is known in classical organic chemistry as neighbouring group participation (N
151 onent reactions are especially attractive in organic chemistry as they allow the synthesis of large l
152 r validates proximity-induced reactivity and organic chemistry as tools not only for chemical tag eng
155 xploring, exposing, and exploiting gas-phase organic chemistry at temperatures of 1000 degrees C and
156 ylides are useful intermediates in synthetic organic chemistry because of their capability of forming
157 e of the most important functional groups in organic chemistry because of their presence in numerous
158 cles is a fundamental challenge in synthetic organic chemistry because the high entropic cost of larg
159 n cutting-edge developments in the fields of organic chemistry, biochemistry, medical research, radic
160 try of Electrocyclic Reactions, ushered into organic chemistry both an explanation of the stereochemi
161 es are highly important functional groups in organic chemistry, both as part of target structures and
162 compounds are in widespread use in synthetic organic chemistry but have untapped potential in chemica
163 ality is a concept that lies at the heart of organic chemistry but is often ignored in discussions of
164 metathesis has had a large impact on modern organic chemistry, but important shortcomings remain: fo
165 building blocks with a unique reactivity in organic chemistry, but only a few reliable methods have
166 enabling transformation in modern synthetic organic chemistry, but there are only limited examples o
168 lute-solvent interactions in modern physical organic chemistry can be studied using supramolecular po
170 eved to be the most passive functionality in organic chemistry, can be reconsidered as a useful funct
171 e of the classical reactive intermediates in organic chemistry-can react in discriminating fashion wi
172 dvent of critical scientific advancements in organic chemistry, chemical analysis, and purification.
174 re user-friendly and broadly utilized by the organic chemistry community to guide and inform the proc
180 of metal-mediated cross-couplings in modern organic chemistry, coupling reactions involving nitrogen
181 surfactants requires expertise in synthetic organic chemistry, creating a barrier to widespread adop
183 c effect, one of the fundamental concepts in organic chemistry, describes the preferences of a substi
184 part from a few compounds under heavy use in organic chemistry, diboranes are relatively exotic and p
185 uted alkenes is a long-standing challenge in organic chemistry, due to the small energy differences b
186 carbon bonds has revolutionized the field of organic chemistry, enabling the efficient synthesis of l
188 ication of Si(001), traditional schemes from organic chemistry for functionalization of alkenes and d
189 en one of the most active research fields in organic chemistry for more than a decade, and it has bee
190 n the understanding of reaction processes in organic chemistry for over 60 years, yet quantitative ap
193 nd could be of interest, in the wide area of organic chemistry, for improving previous processes or f
197 tantial gaps in understanding of atmospheric organic chemistry, hampering efforts to understand, mode
199 biodegradation rules of thumb and some basic organic chemistry has allowed 281 potential PB transform
200 rable attention, but their use in mainstream organic chemistry has been constrained by limitations in
201 understanding of the principles of physical organic chemistry has been essential in all projects.
205 ngle-electron transfer reagents in synthetic organic chemistry has opened up a wealth of possibilitie
210 that a natural language such as English and organic chemistry have the same structure in terms of th
211 al product total synthesis have in advancing organic chemistry, here through the design and realizati
212 werful and convenient synthetic technique in organic chemistry; however, as a general synthetic metho
213 ve demonstrated tremendous utility in modern organic chemistry; however, their application for the sy
215 These studies show the profound role that organic chemistry in general and specifically late-stage
216 responsible for our current understanding of organic chemistry in general, and of natural products ch
218 emperature in the Saturn system, the complex organic chemistry in the atmosphere, from the gas to the
222 lying teaching philosophies that transformed organic chemistry into one of the most popular classes o
223 he use of capsules and cavitands in physical organic chemistry is briefly reviewed, and their applica
225 A general overview on low molecular weight organic chemistry is given, and the applications of hete
226 ental and highly valuable transformations in organic chemistry is the nucleophilic substitution of al
228 um catalysis has become an important tool in organic chemistry, its combination with supramolecular h
231 r reviews how his early love for theoretical organic chemistry led to experimental research and the e
232 igand-receptor complex, along with synthetic organic chemistry, led us to construct a library of smal
233 ysis of hazardous compounds currently in the organic chemistry literature and provide simple "best pr
234 rine bonds are the strongest single bonds in organic chemistry, making activation and cleavage usuall
235 tions employed to date in Microwave-Assisted Organic Chemistry (MAOS) are characterized by the import
236 e across several fields, including synthetic organic chemistry, materials science, targeted drug deli
238 a physical basis for anecdotal evidence that organic chemistry modulates the mineralization of inorga
239 ave critical roles in the areas of synthetic organic chemistry, molecular sensors, materials science,
240 iene isomers of considerable interest to the organic chemistry, molecular spectroscopy, and astrochem
242 ects of an electron-withdrawing group on the organic chemistry of an eta(2)-bound benzene ring are ex
244 stantial opportunities to probe the physical organic chemistry of hopping conduction in long conjugat
246 s in protoplanetary disks, and that the rich organic chemistry of our solar nebula was not unique.
248 become increasingly popular in the field of organic chemistry, offering solutions for engineering an
250 o the aerosol phases, but also the potential organic chemistry on Titan's surface, and in its possibl
252 iting applications in the area of host-guest organic chemistry, or to spectroscopically evaluate in-d
253 emier event sponsored by the ACS Division of Organic Chemistry (ORGN) and has been held in odd-number
257 edstock chemicals remains a central theme in organic chemistry owing to the key roles of amines in sy
258 on in both academic and industrial synthetic organic chemistry owing to their step- and atom-economy
260 rocarbons are important structural motifs in organic chemistry, pharmaceutical chemistry, and materia
261 e least well-studied and understood group in organic chemistry, primarily because their anticipated i
262 dings can be understood from simple physical organic chemistry principles and provide supramolecular
263 action development, focusing on how physical organic chemistry principles have guided probe design.
265 idation have a fundamental role in synthetic organic chemistry, providing functionality that is requi
266 bridized carbon atoms, a fundamental unit of organic chemistry, remains an important yet elusive obje
268 rmance depends on efficient use of synthetic organic chemistry resources, these studies illustrate an
270 of mineralogy, petrography, and isotope and organic chemistry, resulting from a complex formation hi
271 hindrance may come from the adoption of the organic chemistry scheme of molecular description and cl
272 stic experimental and computational physical-organic chemistry studies on 2,6-diarylanilines that con
273 ctive delineates the history of the National Organic Chemistry Symposium (NOS) and, in doing so, trac
274 tion paid to tellurium in both inorganic and organic chemistry textbooks may reflect, in part, the ve
277 tional group manipulations in solution-phase organic chemistry that are heavily used to protect/depro
278 c rules for complex two-dimensional covalent organic chemistry that can be enacted directly at a surf
279 logy to a solution phase thermal reaction in organic chemistry that cannot be otherwise explained usi
281 e, which cannot be synthesized via classical organic chemistry the triplet non-aromatic 2,4,6-cyclooc
282 Because carbonyl groups are ubiquitous in organic chemistry, the ability to synthesize functionali
283 for the introduction of steric hindrance in organic chemistry, the elucidation of the butane rotatio
285 ent excursion into applications of synthetic organic chemistry to neuroscience, avoiding the more-tra
286 hemists harnessed the powerful techniques of organic chemistry to study the functions of organic mole
287 k provides an example of the use of physical organic chemistry to understand an interfacial reaction.
288 trophiles are emerging as a powerful tool in organic chemistry, to date there have been no systematic
289 reaction has quickly found its way into the organic chemistry toolbox and found applications in many
290 Whilst the scope of most of these focuses on organic chemistry, transition-metal catalysis, porous fr
291 ,3-dipolar cycloaddition is commonly used in organic chemistry, we propose that this presents the fir
292 inorganic chemistry, polymer chemistry, and organic chemistry, whereby barriers between these discip
293 henylacetylenes are key structural motifs in organic chemistry, which find widespread applications in
294 ubstantially streamline synthetic efforts in organic chemistry while bypassing substrate activation s
295 tive article describes new roles that modern organic chemistry will need to play in overcoming this c
297 synthesis and application of acylsilanes in organic chemistry, with a particular focus on the progre
299 halides are ubiquitous functional groups in organic chemistry, yet despite their obvious appeal as s
300 sing light is a longstanding practice within organic chemistry, yet little has been done to modulate