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1 lkylamines provides a continual challenge to chemical synthesis.
2 nologies, and advances in library design and chemical synthesis.
3 catalyst and it applications attractive for chemical synthesis.
4 try in contrast with classical approaches of chemical synthesis.
5 tile route to free radical intermediates for chemical synthesis.
6 and tunability that can dramatically improve chemical synthesis.
7 natural sources, recombinant expression, or chemical synthesis.
8 hK polypeptide chains were prepared by total chemical synthesis.
9 ower of rhodium carbene chemistry in organic chemical synthesis.
10 the scope of aerobic oxidation chemistry in chemical synthesis.
11 e knot topologies have been realized through chemical synthesis.
12 s to achieve different product outcomes from chemical synthesis.
13 r the evolution (and at times revolution) in chemical synthesis.
14 le either through biosynthetic precursors or chemical synthesis.
15 oligonucleotide at a fraction of the cost of chemical synthesis.
16 etic materials produced by stereo-controlled chemical synthesis.
17 and catalytic membrane reactors for greener chemical synthesis.
18 rfect example of the intersection of art and chemical synthesis.
19 t, its low reactivity has limited its use in chemical synthesis.
20 poised to realize the potential of solar-to-chemical synthesis.
21 ysts with enormous potential for sustainable chemical synthesis.
22 aximize atom- and step-economy, and simplify chemical synthesis.
23 l main group solid catalysts for sustainable chemical synthesis.
24 ide the inspiration for critical advances in chemical synthesis.
25 new types of one-pot biotransformations for chemical synthesis.
26 oselectivity is of fundamental importance in chemical synthesis.
27 ative fashion is an important goal in modern chemical synthesis.
28 ystems is of utmost importance in nature and chemical synthesis.
29 nm) of natural collagen are recalcitrant to chemical synthesis.
30 izations of alkenes are highly desirable for chemical synthesis.
31 out homogeneous counterparts for sustainable chemical synthesis.
32 but becomes a disadvantage and challenge in chemical synthesis.
33 alysts are critically needed for sustainable chemical synthesis.
34 er reaction has proven a great challenge for chemical synthesis.
35 aditionally avoided reactive intermediate in chemical synthesis.
36 halides are important C-C bond formations in chemical synthesis.
37 s and allenes, opening new opportunities for chemical synthesis.
38 novel approaches to challenging problems in chemical synthesis.
39 ill provide scalability and availability, is chemical synthesis.
40 lizations known, providing a unique tool for chemical synthesis.
41 organoboron species with great potential in chemical synthesis.
42 carbon-heteroatom bond-forming reactions in chemical synthesis.
43 ound them suggested promising candidates for chemical synthesis.
44 d organic building blocks in the large-scale chemical synthesis.
45 r of opportunities in the field of selective chemical synthesis.
46 ly, they present a substantial challenge for chemical synthesis.
47 cules, and they are useful intermediates for chemical synthesis.
48 n product species not directly accessible by chemical synthesis.
49 retical prediction can be tested directly by chemical synthesis.
50 hape-selective catalysis plays a key role in chemical synthesis.
51 age motif of AlbD with substrates derived by chemical synthesis.
52 h electrochemistry for energy conversion and chemical synthesis.
53 olate-type donor substrates and their use in chemical synthesis.
54 ng molecules is a long-standing challenge in chemical synthesis.
55 tro isotopic labelling of this cluster using chemical synthesis.
56 formation are of great importance in modern chemical synthesis.
57 mplemented by protein semisynthesis or total chemical synthesis.
58 control stereochemistry are prized tools in chemical synthesis.
59 cient photocatalysis are highly desirable in chemical synthesis.
60 strategy for initiating radical reactions in chemical synthesis.
61 ydrates remains a long-standing challenge in chemical synthesis.
62 atalyst is expected to bring new insights in chemical synthesis.
63 h photoluminescence quantum yield and facile chemical synthesis.
64 her study of strained alkynes and allenes in chemical synthesis.
65 proach for installing amide functionality in chemical synthesis.
66 atform based on oligosaccharides obtained by chemical synthesis.
67 ecules and provide the foundation for modern chemical synthesis.
68 remain key building blocks in bulk and fine chemical synthesis.
69 e, and mass production compatibility through chemical synthesis.
70 eir structural complexity, which limits bulk chemical synthesis.
71 topologies present an unusual challenge for chemical synthesis and an opportunity for innovation.
72 nfluenza A virus subtype H1N1, and extensive chemical synthesis and analysis of the structure-activit
74 vity relationships, which was facilitated by chemical synthesis and biochemical activity analysis, in
75 Here we report the structure-guided design, chemical synthesis and biological investigations of biva
80 We describe here a new program for virtual chemical synthesis and computational assessment, ChemGen
86 describe the close connection between novel chemical synthesis and optimized light emission by collo
87 NTES-PF4 heterodimer (termed OPRAH) by total chemical synthesis and oxime ligation, with an accelerat
88 ructurally simpler, making it attractive for chemical synthesis and potential applications in biology
89 emselves valuable chiral building blocks for chemical synthesis and precursors to numerous important
92 molecular dynamics simulation program before chemical synthesis and spectral characterizations viz.,
96 of polymers have been used to revolutionize chemical synthesis and the selection of functional nucle
101 to date: in vivo strain manipulation, total chemical synthesis, and chemoenzymatic synthesis methods
102 cysteine makes the molecule more amenable to chemical synthesis, and coupled with its increased class
105 ticle, we use a combination of computations, chemical synthesis, and mechanistic analysis to develop
106 in LC-MS, biochemical ubiquitination assays, chemical synthesis, and protein crystallography to enabl
107 assignments of DHD1 and DHD3, their de novo chemical synthesis, and their production in systems in v
108 e designed CovCore proteins were prepared by chemical synthesis, and their structures were determined
111 es recent advances on use of vinyl azides in chemical synthesis as a radical acceptor and an enamine-
112 alyzed (NHC) transformations are valuable to chemical synthesis, as they can generate high enantiosel
113 pt, this Review is primarily focusing on the chemical synthesis aspects of the ADCs multidisciplinary
114 amongst which 15 peptides were selected for chemical synthesis based on their predicted ACE-I inhibi
116 r sequences and structures, biosynthesis and chemical synthesis, biological functions, and applicatio
117 free energy perturbation (FEP) calculations, chemical synthesis, biophysical mapping and X-ray crysta
118 pplications in the field of enzyme catalyzed chemical synthesis but also enzyme based fuel cells.
119 -metal catalysis has become indispensable to chemical synthesis, but homogeneous high-valent transiti
120 ies, including 2D nanomaterials in colloidal chemical synthesis, but it is still highly challenging t
121 elopment of large-scale solar fuel and solar chemical synthesis, but the poor photovoltages often rep
122 onalization of C(sp(3) )-H bonds streamlines chemical synthesis by allowing the use of simple molecul
123 This review focuses on advances in fine chemical synthesis by titanium-catalyzed reactions featu
124 f natural products, here we demonstrate that chemical synthesis can provide important insights into b
125 e combination of rational design and modular chemical synthesis can revitalize classes of antibiotics
126 metal-mediated hydride transfer reactions in chemical synthesis, catalysis, and biology has inspired
128 ophysical characterization against tractable chemical synthesis: Complexity-building nitro-Mannich/la
130 ,9-EET in this COX pathway were confirmed by chemical synthesis: ct-8,9-epoxy-11-hydroxy-eicosatrieno
131 alkaloid has remained an elusive target for chemical synthesis due to insurmountable issues of react
132 products represent useful intermediates for chemical synthesis due to the versatility of the C-B bon
140 ophilic compounds originating from nature or chemical synthesis have profound effects on immune cells
142 ing potentially valuable building blocks for chemical synthesis, have each been prepared from cyclope
143 recently intensified, thanks to advances in chemical synthesis, improved understanding of charged st
145 il our efforts to prepare these molecules by chemical synthesis, including a photochemical approach,
146 promising approach to tackle this problem is chemical synthesis inside nanocapsules, although enzyme-
148 entified one hit, which was expanded through chemical synthesis into a small panel of potent compound
149 ilico discovered hits have been optimized by chemical synthesis into selective nanomolar compounds, t
150 re l-sugar building blocks through efficient chemical synthesis is a crucial step toward the synthesi
155 tilization of carbon dioxide as feedstock in chemical synthesis, low-energy-barrier CO2 activation is
156 veral other classes of enzymes, but a simple chemical synthesis may have created the first peptides a
161 rides in peptoid monomer model systems using chemical synthesis, NMR spectroscopy, and X-ray crystall
166 tiomer-specific activity and straightforward chemical synthesis of (unnatural) ent-(+)-verticilide pr
167 ffect of such modification, we report here a chemical synthesis of 3F(ax)-Neu5Ac-alpha2,6-Gal as a bu
168 In silico docking and screening, followed by chemical synthesis of a library of quinazolinones, led t
169 to the complex peptide substrate, relying on chemical synthesis of a modified C-terminal fragment and
173 based design efforts in combination with the chemical synthesis of additional molecular entities are
176 based self-assembled nanoparticles, from the chemical synthesis of AMPDs, through nanoparticle prepar
178 To overcome such limitation, the catalyzed chemical synthesis of bacterial PHAs has been developed,
181 difficult for cost-effective production, and chemical synthesis of complex isoprenoids is impractical
182 has long served as a starting point for the chemical synthesis of complex natural products, includin
185 instructed specific living neurons to guide chemical synthesis of electrically functional (conductiv
187 de nucleic acids (PNA), we herein report the chemical synthesis of fluorinated PNA monomers and bioph
191 Here, we report a new method for the total chemical synthesis of IGF-1 analogs, which entails the s
193 structure-activity relationships enabled the chemical synthesis of LCL204, with enhanced inhibitory p
195 protocol consists of four major stages: (i) chemical synthesis of MPNs, (ii) conjugation with DNA an
196 The incorporation of impurities during the chemical synthesis of nanomaterials is usually uncontrol
199 ase peptide synthesis as demonstrated in the chemical synthesis of NEDD8 protein, without the use of
201 onstrate the utility of this approach by the chemical synthesis of nine different protein chains that
202 nventional methods for natural extraction or chemical synthesis of O-PS are technically demanding, in
208 owever, the utility of this functionality in chemical synthesis of peptides and proteins remains unex
209 unctionalized silica resin to facilitate the chemical synthesis of peptides in organic solvent as wel
210 he first example of the use of non-enzymatic chemical synthesis of phospholipids to prepare proteolip
214 hemical definition and solubility, while the chemical synthesis of polysaccharides is challenging wit
218 tion of sulfonated-PCBs was confirmed by the chemical synthesis of reference standards, obtained thro
220 r previous research in this area through the chemical synthesis of six site-specifically O-GlcNAcylat
221 The routes that have been taken for the chemical synthesis of such nucleoside derivatives are de
222 is a powerful synthetic methodology for the chemical synthesis of technologically important biodegra
232 at we validated through performing the first chemical synthesis of the two natural products Tasipepti
233 a promising green alternative to the current chemical synthesis of these esters of unquestionable nut
234 ix different research groups have reported a chemical synthesis of this compound, five of which used
239 h-resolution mass spectrometry platform, and chemical synthesis of well-defined HS oligosaccharides f
240 ive update on the properties (structural and chemical), synthesis of sulfide solid-state electrolytes
241 tions including the destruction of hazardous chemicals, synthesis of organic compounds, and many othe
245 ging task due to the complexity in multistep chemical synthesis or the inability of the biosynthetic
246 ke features, and synthetic accessibility for chemical synthesis, out of 593 hits, 39 were left top hi
252 aulobacter crescentus through the process of chemical synthesis rewriting and studied the genetic inf
253 In sum, our results highlight the promise of chemical synthesis rewriting to decode fundamental genom
254 n, we report on a first direct aqueous-phase chemical synthesis route to NIR PLNPs and present their
255 nosheets are synthesized using a one-pot wet-chemical synthesis route with and without Re doping.
257 s play an important role such as fuel cells, chemical synthesis, self-assembly, catalysis and surface
259 Structural verification and modification by chemical synthesis showed that O4I1 and its derivatives
260 ily, was prepared for the first time through chemical synthesis starting from 2,3-dimethylbutadiene.
261 epared via two methods: (1) conventional wet chemical synthesis (strong electrostatic adsorption-SEA)
262 based on first-principles methods including chemical synthesis, structure elucidation and standard-a
265 Here, we report a step toward a paradigm of chemical synthesis that relieves chemists from routine t
266 ediate to many potent Illicium terpenes make chemical synthesis the unquestionable method for accessi
267 amongst the most studied reactions in all of chemical synthesis, the number of reactions that apply t
268 ional groups, rarely does one consider using chemical synthesis to add molecular complexity to the na
269 tope labeling, tandem mass spectrometry, and chemical synthesis to deduce the structure of colibactin
270 an untargeted DNA adductomics approach with chemical synthesis to identify and characterize a covale
271 erent extraction approaches from tea shoots, chemical synthesis to microbial transformation have been
272 We used whole-genome design and complete chemical synthesis to minimize the 1079-kilobase pair sy
273 lies on bioinformatic algorithms followed by chemical synthesis to predict and then produce small mol
275 extensive modification by mutagenesis and/or chemical synthesis to prevent rapid in vivo degradation.
276 Overall, the study demonstrates the power of chemical synthesis to produce natural product variants w
277 to predict the output of a BGC and in vitro chemical synthesis to produce the predicted structure.
281 t they present challenging issues of complex chemical synthesis, undesirable physical properties, and
282 lop a scalable, cost-effective and versatile chemical synthesis using a fired brick to control oxidat
289 lengths and N- and O-sulfation patterns via chemical synthesis were systematically studied about the
290 iven to some of the recent advances in their chemical synthesis which allows not only the preparation
291 ptide, albopeptide, through NMR analysis and chemical synthesis, which contains two contiguous unsatu
292 esponsive materials offers simple design and chemical synthesis while enabling different stimuli to p
293 igomers and unnatural variants produced from chemical synthesis will allow for further detailed struc
294 e use of biocatalytic methods in the area of chemical synthesis with focused attention on retrosynthe
295 nt two important strategies for eco-friendly chemical synthesis with high atom efficiency and reduced
296 This approach combined the flexibility of chemical synthesis with the selectivity of enzyme-cataly
298 zyme activities that have been exploited for chemical synthesis, with an emphasis on reactions that d