The Deuterated "Magic Methyl" Group: A Guide to Site-Selective Trideuteromethyl Incorporation and Labeling by Using CD3 Reagents

被引:72
作者
Steverlynck, Joost [1 ]
Sitdikov, Ruzal [1 ]
Rueping, Magnus [1 ,2 ]
机构
[1] King Abdullah Univ Sci & Technol KAUST, Kaust Catalysis Ctr KCC, Thuwal 239556900, Saudi Arabia
[2] Rhein Westfal TH Aachen, Forckenbeckstr 55, D-52074 Aachen, Germany
关键词
C-C coupling; C-1 building blocks; deuterium; medicinal chemistry; methylation; CATALYZED ALPHA-METHYLATION; UNACTIVATED C(SP(3))-H BONDS; C-H METHYLATION; N-METHYLATION; DIMETHYL CARBONATE; ALLYLIC ALCOHOLS; ACID-DERIVATIVES; FENTON-LIKE; ALKYLATION; DISCOVERY;
D O I
10.1002/chem.202101179
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In the field of medicinal chemistry, the precise installation of a trideuteromethyl group is gaining ever-increasing attention. Site-selective incorporation of the deuterated "magic methyl" group can provide profound pharmacological benefits and can be considered an important tool for drug optimization and development. This review provides a structured overview, according to trideuteromethylation reagent, of currently established methods for site-selective trideuteromethylation of carbon atoms. In addition to CD3, the selective introduction of CD2H and CDH2 groups is also considered. For all methods, the corresponding mechanism and scope are discussed whenever reported. As such, this review can be a starting point for synthetic chemists to further advance trideuteromethylation methodologies. At the same time, this review aims to be a guide for medicinal chemists, offering them the available C-CD3 formation strategies for the preparation of new or modified drugs.
引用
收藏
页码:11751 / 11772
页数:22
相关论文
共 235 条
[1]   Deuterated abscisic acid analogs for mass spectrometry and metabolism studies [J].
Abrams, SR ;
Nelson, K ;
Ambrose, SJ .
JOURNAL OF LABELLED COMPOUNDS & RADIOPHARMACEUTICALS, 2003, 46 (03) :273-283
[2]   Stereochemistry of hydroxylation during the conversion of alpha-ketoisocaproate to beta-hydroxyisovalerate by 4-hydroxyphenylpyruvate dioxygenase [J].
Adlington, RM ;
Baldwin, JE ;
Crouch, NP ;
Lee, MH ;
MacKinnon, CH ;
Paul, DR .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 1996, 6 (22) :2721-2724
[3]   Biphenyl amide p38 kinase inhibitors 3: Improvement of cellular and in vivo activity [J].
Angell, Richard ;
Aston, Nicola M. ;
Bamborough, Paul ;
Buckton, Jacky B. ;
Cockerill, Stuart ;
deBoeck, Suzanne J. ;
Edwards, Chris D. ;
Holmes, Duncan S. ;
Jones, Katherine L. ;
Laine, Dramane I. ;
Patel, Shila ;
Smee, Penny A. ;
Smith, Kathryn J. ;
Somers, Don O. ;
Walker, Ann L. .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2008, 18 (15) :4428-4432
[4]  
[Anonymous], 2021, ANGEW CHEM, V133, P6427
[5]  
[Anonymous], 2018, ANGEW CHEM, V130, P15779
[6]  
[Anonymous], 2013, ANGEW CHEM, V125, P12480
[7]  
[Anonymous], 2017, ANGEW CHEM, V129, P9335
[8]  
[Anonymous], 2014, ANGEW CHEM
[9]  
[Anonymous], 2019, ANGEW CHEM, V131, P785
[10]  
[Anonymous], 2017, ANGEW CHEM, V129, P3402