Intermolecular Reaction Screening as a Tool for Reaction Evaluation

被引:97
作者
Collins, Karl D. [1 ]
Glorius, Frank [1 ]
机构
[1] Univ Munster, Inst Organ Chem, D-48149 Munster, Germany
关键词
C-H ACTIVATION; N-TYPE REACTIONS; ROBUSTNESS SCREEN; RAPID ASSESSMENT; CATALYST; DISCOVERY; COUPLINGS; FUNCTIONALIZATION; ACETOXYLATION; ALKYNYLATION;
D O I
10.1021/ar500434f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
CONSPECTUS: Synthetic organic chemistry underpins many scientific disciplines. The development of new synthetic methods proceeds with the ultimate intention of providing access to novel structural motifs or providing safer, increasingly efficient, or more economical chemical reactions. To facilitate the identification and application of new methods in solving real synthetic problems, this Account will highlight the benefits of providing a fuller picture of both the scope and limitations of new reactions, with a primary focus on the evaluation of functional group tolerance and stability of a reaction using intermolecular screens. This Account will begin with a discussion on reaction evaluation, specifically considering the suitability of a given reaction for application in target-oriented synthesis. A comparison of desirable and essential criteria when choosing a reaction is given, and a short discussion on the value of negative and qualitative data is provided. The concept of intermolecular reaction screening will be introduced, and a direct comparison with a traditional substrate scope highlights the benefits and limitations of each and thus the complementary nature of these approaches. In recent years, a number of ad hoc applications of intermolecular screens to evaluate the functional group tolerance of a reaction or the stability of functional groups to a given set of reaction conditions have been reported, and will be discussed. More recently, we have developed a formal high-throughput intermolecular screening protocol that can be utilized to rapidly evaluate new chemical reactions. This simple and rapid protocol enables a much broader evaluation of a reaction in terms of functional group tolerance and the stability of chemical motifs to the reaction conditions than is feasible with a typical reaction scope. The development, evaluation, and application of this method within our group will be discussed in detail, with both the potential benefits and limitations highlighted and discussed. In addition, we will discuss more recent applications of intermolecular screens from both industrial and academic groups. Modifications in protocols and applications will be highlighted, including problem based evaluations, assessment of biomolecule compatibility, establishment of relative rate data, and the identification of new reactivity. Such screens have been applied in diverse chemistries including C-H functionalization reactions, frustrated Lewis-pair-catalyzed hydrogenations, heterogeneous catalysis, photoredox catalysis, enantioselective organocatalysis, and polymer science. We feel that the application of intermolecular screens to such a diversity of reactions highlights the practical simplicity of such screens. A summary of the applications and potential utility of intermolecular reaction evaluation is provided.
引用
收藏
页码:619 / 627
页数:9
相关论文
共 40 条
[1]   Iron-Catalyzed Borylation of Alkyl Electrophiles [J].
Atack, Thomas C. ;
Lecker, Rachel M. ;
Cook, Silas P. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2014, 136 (27) :9521-9523
[2]   Designer substrate library for quantitative, predictive modeling of reaction performance [J].
Bess, Elizabeth N. ;
Bischoff, Amanda J. ;
Sigman, Matthew S. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2014, 111 (41) :14698-14703
[3]  
Billiet S, 2014, NAT CHEM, V6, P815, DOI [10.1038/nchem.2023, 10.1038/NCHEM.2023]
[4]   A Mild, Palladium-Catalyzed Method for the Dehydrohalogenation of Alkyl Bromides: Synthetic and Mechanistic Studies [J].
Bissember, Alex C. ;
Levina, Anna ;
Fu, Gregory C. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2012, 134 (34) :14232-14237
[5]   Using Rh(III)-Catalyzed C-H Activation as a Tool for the Selective Functionalization of Ketone-Containing Molecules [J].
Boultadakis-Arapinis, Melissa ;
Hopkinson, Matthew N. ;
Glorius, Frank .
ORGANIC LETTERS, 2014, 16 (06) :1630-1633
[6]   Allylic C-H Acetoxylation with a 4,5-Diazafluorenone-Ligated Palladium Catalyst: A Ligand-Based Strategy To Achieve Aerobic Catalytic Turnover [J].
Campbell, Alison N. ;
White, Paul B. ;
Guzei, Ilia A. ;
Stahl, Shannon S. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2010, 132 (43) :15116-15119
[7]   Serial ligand catalysis: A highly selective allylic C-H oxidation [J].
Chen, MS ;
Prabagaran, N ;
Labenz, NA ;
White, MC .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (19) :6970-6971
[8]   REACTION METHODOLOGY Speed dating for reactions [J].
Churcher, Ian .
NATURE CHEMISTRY, 2013, 5 (07) :554-555
[9]  
Collins KD, 2014, NAT CHEM, V6, P859, DOI [10.1038/nchem.2062, 10.1038/NCHEM.2062]
[10]   Application of a robustness screen for the evaluation of synthetic organic methodology [J].
Collins, Karl D. ;
Ruehling, Andreas ;
Glorius, Frank .
NATURE PROTOCOLS, 2014, 9 (06) :1348-1353