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1  applications in bioorthogonal chemistry and natural product synthesis.
2             The reaction can also be used in natural product synthesis.
3 ptual disconnections in the arena of steroid natural product synthesis.
4 xtension of these tools to encompass complex natural product synthesis.
5 s and silyl ethers and their applications to natural product synthesis.
6 l of C-C activation for streamlining complex natural product synthesis.
7 evelopment of new methods and strategies for natural product synthesis.
8 has fueled advances in aryne methodology and natural product synthesis.
9 n in the context of both pharmaceuticals and natural product synthesis.
10 terest due to the role of these organisms in natural product synthesis.
11 ence of strained alkenes as intermediates in natural product synthesis.
12  addition, arynes have found applications in natural product synthesis.
13 ethod development as well as applications to natural product synthesis.
14  a process that is potentially applicable to natural product synthesis.
15  racemic reaction partners in the context of natural product synthesis.
16 ation of two recently developed reactions to natural product synthesis.
17 olves a longstanding problem in the field of natural product synthesis.
18  + 2] cycloaddition of chiral allenamides in natural product synthesis.
19 hat are important to medicinal chemistry and natural product synthesis.
20  which are valuable chiral intermediates for natural product synthesis.
21 ining fragments with relevance to polyketide natural product synthesis.
22 tilized these compounds as intermediates for natural product synthesis.
23 roduction of halogen atoms in the context of natural product synthesis.
24 ddition that has not been used previously in natural product synthesis.
25 e easily functionalized allowing an entry to natural products synthesis.
26                   A retrospective account of natural products synthesis adopting the Chiral Synthon (
27  future utility of these chemical methods in natural product synthesis and medicinal chemistry.
28 ed hydrindane-forming annulation reaction in natural product synthesis and the first total synthesis
29 hoxycyclohexanone building blocks for use in natural products synthesis and medicinal chemistry.
30 thilone A could open up new possibilities in natural-product synthesis and, together with solution-ph
31 this reaction, highlighting its potential in natural product synthesis applications.
32 nsymmetrical biaryls play an evident role in natural product synthesis, as ligand systems in homogene
33 amely organocascade catalysis and collective natural product synthesis, can facilitate the preparatio
34  of this pyrroloindoline-forming reaction to natural product synthesis has been accomplished in the c
35 agment coupling reaction of great utility in natural product synthesis has emerged.
36 pplications of the squarate ester cascade to natural products synthesis have been realized.
37 lm phenotypes further validating the role of natural product synthesis in the discovery of new biolog
38 ts in cascade polycyclizations as applied to natural product synthesis, including pericyclic, heteroa
39 ceptor cyclopropanes as reactive subunits in natural product synthesis is underscored.
40 ful intermediates in medicinal chemistry and natural products synthesis, is reported.
41 metrization of a centrosymmetric molecule in natural product synthesis: Jacobsen asymmetric epoxide h
42 nthetic endeavors, such as drug discovery or natural product synthesis, large quantities of material
43 n, zinc, and indium and their application to natural product synthesis over the past quarter century.
44 cesses for reactions commonly encountered in natural product synthesis programs to achieve the first
45 d synthetic tool with impressive examples in natural product synthesis reported in recent years.
46 droxybenzaldehyde as a starting material for natural product synthesis through the use sequential o-q
47      This reflects a process of evolution of natural product synthesis which has accelerated in the y
48 onalized conjugated dienes can be adapted to natural product synthesis with great effect.

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