ライフサイエンスコーパス: organic chemistry

1 esis as well as the parallels with synthetic organic chemistry.

2 milarities to the Birch reduction known from organic chemistry.

3 ling opens unique opportunities in synthetic organic chemistry.

4 to proposed mechanisms based on knowledge of organic chemistry.

5 try and important synthetic intermediates in organic chemistry.

6 lization is a central challenge in synthetic organic chemistry.

7 ve recently gained attention in the field of organic chemistry.

8 development of new and useful strategies in organic chemistry.

9 on reactions is a long-standing challenge in organic chemistry.

10 ins one of the most formidable challenges in organic chemistry.

11 for their synthesis is an important goal in organic chemistry.

12 g reactions remains an unsolved challenge in organic chemistry.

13 are considered important synthetic tools in organic chemistry.

14 eaction has long been a contentious issue in organic chemistry.

15 mited attention and application in synthetic organic chemistry.

16 as re-emerged as a major target of synthetic organic chemistry.

17 versus nonbiological catalysis in synthetic organic chemistry.

18 ined with some of the most heated debates in organic chemistry.

19 of the bond renders it the strongest one in organic chemistry.

20 ng the most commonly used switching units in organic chemistry.

21 t versatile of all reactive intermediates in organic chemistry.

22 nion has fundamental importance to synthetic organic chemistry.

23 lecules represents a formidable challenge in organic chemistry.

24 significant transformations in contemporary organic chemistry.

25 is emerging as a powerful tool in synthetic organic chemistry.

26 their use as powerful reagents in synthetic organic chemistry.

27 are versatile building blocks for synthetic organic chemistry.

28 uld find widespread application in synthetic organic chemistry.

29 eaction has long been a contentious issue in organic chemistry.

30 ive strategies for molecular construction in organic chemistry.

31 hemical depletion of which furnishes Titan's organic chemistry.

32 ns are employed extensively in many areas of organic chemistry.

33 soon rival and potentially eclipse synthetic organic chemistry.

34 occupy well-established ground in classical organic chemistry.

35 oscopy as a standard analytical technique in organic chemistry.

36 is an entrenched synthetic disconnection in organic chemistry.

37 other water molecules and allows for a rich organic chemistry.

38 ated C-H bond remains a central challenge in organic chemistry.

39 s a longstanding and formidable challenge in organic chemistry.

40 omprehensive way the structural diversity of organic chemistry.

41 er disk and that the disk supports an active organic chemistry.

42 ectrophiles are important transformations in organic chemistry.

43 nucleophile is of fundamental importance in organic chemistry.

44 key factor in shaping the known universe of organic chemistry.

45 ation, much as synthetic approaches informed organic chemistry.

46 seeding newly formed planets with prebiotic organic chemistry.

47 rable relevance to biosynthetic reactions in organic chemistry.

48 should become a useful synthon in synthetic organic chemistry.

49 cular interest as a biocatalyst in synthetic organic chemistry.

50 hich are valuable synthetic intermediates in organic chemistry.

51 international membership by promoting modern organic chemistry.

52 lass of compounds across a broad spectrum of organic chemistry.

53 ding of structure/activity relationships, in organic chemistry.

54 liodonium salts in preparative and synthetic organic chemistry.

55 play an ever increasing role in contemporary organic chemistry.

56 servations on the protean nature of physical organic chemistry.

57 enzymes work beyond the tenants of physical organic chemistry.

58 ross the broad spectrum of polymer-supported organic chemistry.

59 tudied and widely used class of reactions in organic chemistry.

60 ortance for the synthesis of pure samples in organic chemistry.

61 ntal lineC bonds is a ubiquitous reaction in organic chemistry.

62 same time one of the youngest disciplines of organic chemistry.

63 ies, many of which are legendary in physical organic chemistry.

64 roaches of fullerenes are the holy grail for organic chemistry.

65 rful carbon-carbon-bond-forming reactions in organic chemistry.

66 ution to unaddressed challenges in synthetic organic chemistry.

67 nts an environmentally benign methodology in organic chemistry.

68 ortant in plantery atmospheres and synthetic organic chemistry.

69 alpha and beta silicon effects from physical organic chemistry.

70 olecules, as well as useful intermediates in organic chemistry.

71 ions and the resulting impact on atmospheric organic chemistry.

72 Aromaticity is a key concept in organic chemistry.

73 in fields such as pharmaceutical science and organic chemistry.

74 y to possess richer chemistry than the known organic chemistry.

75 ortant classes of isomerization reactions in organic chemistry.

76 r constructing carbon-carbon double bonds in organic chemistry.

77 the beginning of a synergy between WGSR and organic chemistry.

78 a prominent role in both drug discovery and organic chemistry.

79 hus far been achieved only through synthetic organic chemistry.

80 inones are common stoichiometric reagents in organic chemistry.

81 anilines has been a significant challenge in organic chemistry.

82 is one of the archetypal transformations of organic chemistry.

83 ual property of a facially polarized ring in organic chemistry.

84 ironmentally benign reduction methodology in organic chemistry.

85 fundamentally important functional groups in organic chemistry.

86 ee) compounds remains a challenge in modern organic chemistry.

87 tereoselectively, are central to research in organic chemistry.

88 rkable versatility and efficacy in synthetic organic chemistry, 38C2 has been used for the selective

89 cal techniques of molecular-level control in organic chemistry, allow preparation of well-defined pol

90 However, the more sophisticated organic chemistry, almost totally inside cells until hum

91 from the perspective of fundamental physical organic chemistry and aid in understanding their behavio

92 enations constitute fundamental processes in organic chemistry and allow for atom-efficient and clean

93 ast class of extremely versatile reagents in organic chemistry and are particularly useful in the pre

94 Small molecules play a fundamental role in organic chemistry and biology.

95 Hence the variability of reductive cellular organic chemistry and its limitations in cells have to b

96 trategy for chemical synthesis that combines organic chemistry and metabolic engineering.

97 The interface between synthetic organic chemistry and natural products was explored in o

98 N102 demonstrates that, by bringing together organic chemistry and neuroscience, molecular entities c

99 up transformations are applicable in general organic chemistry and not restricted to carbohydrate che

100 e NOS played in the launch of The Journal of Organic Chemistry and Organic Reactions and the initiati

101 ry and structure in the rapid development of organic chemistry and physical organic chemistry over th

102 athesis (CM) reaction is used extensively in organic chemistry and represents a powerful method for t

103 My sojourn from classical physical-organic chemistry and solvolysis to self-assembly and su

104 By combination of synthetic organic chemistry and structure-based design, two select

105 de organic materials, and recent progress in organic chemistry and surface chemistry has led to the s

106 lysed transformations are a powerful tool in organic chemistry and the enormous progress, which has b

107 It is a tribute to developments in organic chemistry and the field of organic synthesis tha

108 n bond formation is an essential reaction in organic chemistry and the use of aldolase enzymes for th

109 allenge traditional applications of physical organic chemistry and transition-state theory to enzymat

110 act many research areas, including medicine, organic chemistry, and cell biology.

111 Advances in molecular biology, organic chemistry, and materials science have recently c

112 tral to the origin of life, is emergent from organic chemistry, and may be unique.

113 ve played a prominent role in the history of organic chemistry, and they continue to be important as

114 y and selectivity is at the core of physical organic chemistry, and this knowledge can be used to inf

115 The C-F bond is the most polar bond in organic chemistry, and thus the bond has a relatively la

116 to test the scope of heavy-atom tunneling in organic chemistry, and to check the accuracy of one-dime

117 wn to be powerful biocatalysts for synthetic organic chemistry applications and were also suggested t

118 oven their versatility as synthetic tools in organic chemistry, are currently on the rise in fluorina

119 redox catalysis has come to the forefront in organic chemistry as a powerful strategy for the activat

120 Protonated epoxides feature prominently in organic chemistry as reactive intermediates.

121 onent reactions are especially attractive in organic chemistry as they allow the synthesis of large l

122 r validates proximity-induced reactivity and organic chemistry as tools not only for chemical tag eng

123 potential applications in both inorganic and organic chemistry, as well as materials science.

124 A majority of work focuses on the rich organic chemistry associated with photochemically initia

125 xploring, exposing, and exploiting gas-phase organic chemistry at temperatures of 1000 degrees C and

126 e of the most important functional groups in organic chemistry because of their presence in numerous

127 try of Electrocyclic Reactions, ushered into organic chemistry both an explanation of the stereochemi

128 compounds are in widespread use in synthetic organic chemistry but have untapped potential in chemica

129 ality is a concept that lies at the heart of organic chemistry but is often ignored in discussions of

130 metathesis has had a large impact on modern organic chemistry, but important shortcomings remain: fo

131 enabling transformation in modern synthetic organic chemistry, but there are only limited examples o

132 he molecular step-by-step routes afforded to organic chemistry by total synthesis.

133 at a biochemist without specific training in organic chemistry can perform the synthesis.

134 eved to be the most passive functionality in organic chemistry, can be reconsidered as a useful funct

135 e of the classical reactive intermediates in organic chemistry-can react in discriminating fashion wi

136 re user-friendly and broadly utilized by the organic chemistry community to guide and inform the proc

137 have generated significant interest from the organic chemistry community.

138 al process, it is underused by the synthetic organic chemistry community.

139 One of the marquis challenges in modern Organic Chemistry concerns the design and synthesis of a

140 An important question in organic chemistry concerns the extent to which benzynes-

141 Applications to recent experiments in organic chemistry (counterintuitive Lewis base stabiliza

142 surfactants requires expertise in synthetic organic chemistry, creating a barrier to widespread adop

143 part from a few compounds under heavy use in organic chemistry, diboranes are relatively exotic and p

144 roteins accessible to the tools of synthetic organic chemistry, enabling the covalent structure of pr

145 carbon bonds has revolutionized the field of organic chemistry, enabling the efficient synthesis of l

146 equilibrium processes in fields as varied as organic chemistry, enzymology, or protein folding.

147 ication of Si(001), traditional schemes from organic chemistry for functionalization of alkenes and d

148 en one of the most active research fields in organic chemistry for more than a decade, and it has bee

149 n the understanding of reaction processes in organic chemistry for over 60 years, yet quantitative ap

150 actions have played an indispensable role in organic chemistry for the last several decades.

151 A central idea in organic chemistry for the past 50 years is that cyclopro

152 nd could be of interest, in the wide area of organic chemistry, for improving previous processes or f

153 Although this route is central in organic chemistry, for materials synthesis the low opera

154 The case is made for transitioning organic chemistry from a developed discipline that remai

155 Enzymes as catalysts in synthetic organic chemistry gained importance in the latter half o

156 tantial gaps in understanding of atmospheric organic chemistry, hampering efforts to understand, mode

157 biodegradation rules of thumb and some basic organic chemistry has allowed 281 potential PB transform

158 The utility of POP supports in solid-phase organic chemistry has also been demonstrated successfull

159 rable attention, but their use in mainstream organic chemistry has been constrained by limitations in

160 understanding of the principles of physical organic chemistry has been essential in all projects.

161 For the past 75 years, physical organic chemistry has been the foundation for the elucid

162 In the past century, systematic organic chemistry has been the major approach for produc

163 Naturally, this area of organic chemistry has experienced rapid growth over the

164 Organic chemistry has made possible the synthesis of mol

165 ngle-electron transfer reagents in synthetic organic chemistry has opened up a wealth of possibilitie

166 that the principles and methods of physical organic chemistry have adapted well to the study of orga

167 Selectivity rules in organic chemistry have been inferred largely from nonaqu

168 While triumphs in organic chemistry have enabled the establishment and sus

169 Advances in synthetic organic chemistry have enabled the preparation and subse

170 that a natural language such as English and organic chemistry have the same structure in terms of th

171 Photonic materials generated via organic chemistry have yet to surpass the native protein

172 linear free-energy relationships of physical organic chemistry, have suggested a transition-state str

173 werful and convenient synthetic technique in organic chemistry; however, as a general synthetic metho

174 The study of organic chemistry in atmospheric aerosols and cloud form

175 These studies show the profound role that organic chemistry in general and specifically late-stage

176 responsible for our current understanding of organic chemistry in general, and of natural products ch

177 The highly refined organic chemistry in solid-phase synthesis has made it t

178 emperature in the Saturn system, the complex organic chemistry in the atmosphere, from the gas to the

179 y new, virtually irreversible, inorganic and organic chemistry in the environment, much of it new mod

180 The role played by organic chemistry in the pharmaceutical industry continu

181 In addition, exploring organic chemistry in water can lead to uncommon reactivi

182 zobenzene-based surfactant was described for organic chemistry in water.

183 Physical organic chemistry, in turn, provides structural insight,

184 a number of misunderstandings concerning the organic chemistry involved.

185 he use of capsules and cavitands in physical organic chemistry is briefly reviewed, and their applica

186 Organic chemistry is continually evolving to improve the

187 A general overview on low molecular weight organic chemistry is given, and the applications of hete

188 A common strategy in organic chemistry is to utilize different solvents to in

189 e most versatile of the functional groups in organic chemistry, it is absent in the genetically encod

190 um catalysis has become an important tool in organic chemistry, its combination with supramolecular h

191 flow flash chromatography widely employed in organic chemistry laboratories.

192 entional equipment familiar to a traditional organic chemistry laboratory are being replaced.

193 r reviews how his early love for theoretical organic chemistry led to experimental research and the e

194 igand-receptor complex, along with synthetic organic chemistry, led us to construct a library of smal

195 rine bonds are the strongest single bonds in organic chemistry, making activation and cleavage usuall

196 tions employed to date in Microwave-Assisted Organic Chemistry (MAOS) are characterized by the import

197 Physical organic chemistry might be regarded as officially recogn

198 a physical basis for anecdotal evidence that organic chemistry modulates the mineralization of inorga

199 ave critical roles in the areas of synthetic organic chemistry, molecular sensors, materials science,

200 ects of an electron-withdrawing group on the organic chemistry of an eta(2)-bound benzene ring are ex

201 ive intermediates, specifically the physical organic chemistry of carbenes and carbocations.

202 stantial opportunities to probe the physical organic chemistry of hopping conduction in long conjugat

203 s in protoplanetary disks, and that the rich organic chemistry of our solar nebula was not unique.

204 which may also find application in synthetic organic chemistry of phosphorus(III) and (V).

205 one of the of the iconic figures in physical organic chemistry of the 20th century.

206 d inorganic chemistry and, most notably, the organic chemistry of the transition metals, and the cont

207 become increasingly popular in the field of organic chemistry, offering solutions for engineering an

208 be performed in what we have termed physical organic chemistry on the brain.

209 o the aerosol phases, but also the potential organic chemistry on Titan's surface, and in its possibl

210 Just as synthetic organic chemistry once revolutionized the ability of che

211 iting applications in the area of host-guest organic chemistry, or to spectroscopically evaluate in-d

212 emier event sponsored by the ACS Division of Organic Chemistry (ORGN) and has been held in odd-number

213 my group's research contributions in metallo-organic chemistry over the past 40 years.

214 and, in doing so, traces the development of organic chemistry over the past 88 years.

215 evelopment of organic chemistry and physical organic chemistry over the past century.

216 simple models that are part of the fabric of organic chemistry pedagogy.

217 rocarbons are important structural motifs in organic chemistry, pharmaceutical chemistry, and materia

218 at a time and applying knowledge of physical-organic chemistry, predictive rules are under developmen

219 e least well-studied and understood group in organic chemistry, primarily because their anticipated i

220 sized creatine fatty esters through original organic chemistry process.

221 idation have a fundamental role in synthetic organic chemistry, providing functionality that is requi

222 bridized carbon atoms, a fundamental unit of organic chemistry, remains an important yet elusive obje

223 The potential impact of this methodology on organic chemistry research is discussed.

224 rmance depends on efficient use of synthetic organic chemistry resources, these studies illustrate an

225 ad application in the areas of inorganic and organic chemistry, respectively.

226 of mineralogy, petrography, and isotope and organic chemistry, resulting from a complex formation hi

227 hindrance may come from the adoption of the organic chemistry scheme of molecular description and cl

228 stic experimental and computational physical-organic chemistry studies on 2,6-diarylanilines that con

229 ctive delineates the history of the National Organic Chemistry Symposium (NOS) and, in doing so, trac

230 cts of what is conventionally referred to in organic chemistry textbooks as electrophilic aromatic br

231 tion paid to tellurium in both inorganic and organic chemistry textbooks may reflect, in part, the ve

232 Despite the fact that most organic chemistry textbooks say far more about how struc

233 ll remains restricted to planar molecules in organic chemistry textbooks.

234 tional group manipulations in solution-phase organic chemistry that are heavily used to protect/depro

235 c rules for complex two-dimensional covalent organic chemistry that can be enacted directly at a surf

236 logy to a solution phase thermal reaction in organic chemistry that cannot be otherwise explained usi

237 on is that data in the Beilstein Handbook of Organic Chemistry that have been claimed to support the

238 New catalytic synthetic methods in organic chemistry that satisfy increasingly stringent en

239 lain both this observation, and the physical-organic chemistry that underlies it.

240 e, which cannot be synthesized via classical organic chemistry the triplet non-aromatic 2,4,6-cyclooc

241 Because carbonyl groups are ubiquitous in organic chemistry, the ability to synthesize functionali

242 for the introduction of steric hindrance in organic chemistry, the elucidation of the butane rotatio

243 ich our group has used the tools of physical organic chemistry to investigate the mechanisms of a var

244 has undergone from mechanistic and synthetic organic chemistry to natural products chemistry.

245 ent excursion into applications of synthetic organic chemistry to neuroscience, avoiding the more-tra

246 hemists harnessed the powerful techniques of organic chemistry to study the functions of organic mole

247 k provides an example of the use of physical organic chemistry to understand an interfacial reaction.

248 trophiles are emerging as a powerful tool in organic chemistry, to date there have been no systematic

249 physics, ranging from Hammond's postulate in organic chemistry, to the relaxation dynamics of complex

250 reaction has quickly found its way into the organic chemistry toolbox and found applications in many

251 ,3-dipolar cycloaddition is commonly used in organic chemistry, we propose that this presents the fir

252 inorganic chemistry, polymer chemistry, and organic chemistry, whereby barriers between these discip

253 ubstantially streamline synthetic efforts in organic chemistry while bypassing substrate activation s

254 tive article describes new roles that modern organic chemistry will need to play in overcoming this c

255 This field of science combines organic chemistry with polymerase engineering to create

256 synthesis and application of acylsilanes in organic chemistry, with a particular focus on the progre

257 Whereas organic chemistry would have predicted the ring size and

258 sing light is a longstanding practice within organic chemistry, yet little has been done to modulate