Traceless directing groups: a novel strategy in regiodivergent C-H functionalization

被引:85
作者
Rani, Geetika [1 ]
Luxami, Vijay [1 ]
Paul, Kamaldeep [1 ]
机构
[1] Thapar Inst Engn & Technol, Sch Chem & Biochem, Patiala 147001, Punjab, India
关键词
ARYL CARBOXYLIC-ACIDS; N-N BOND; INDOLE SYNTHESIS; BENZOIC-ACIDS; ORTHOGONAL SELECTIVITY; CATALYZED SYNTHESIS; ORTHO-HALOGENATION; ALIPHATIC ALKENES; DIRECT ARYLATION; DIAZO-COMPOUNDS;
D O I
10.1039/d0cc04863a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The use of functional groups as internal ligands for assisting C-H functionalization, termed the chelation assisted strategy, is emerging as one of the most powerful tools for construction of C-C and C-X bonds from inert C-H bonds. However, there are various directing groups which cannot be either removed after functionalization or require some additional steps or reagents for their removal, thereby limiting the scope of structural diversity of the products, and the step and atom economy of the system. These limitations are overcome by the use of the traceless directing group (TDG) strategy wherein functionalization of the substrate and removal of the directing group can be carried out in a one pot fashion. Traceless directing groups serve as the most ideal chelation assisted strategy with a high degree of reactivity and selectivity without any requirement for additional steps for their removal. The present review overviews the use of various functional groups such as carboxylic acids, aldehydes, N-oxides, nitrones, N-nitroso amines, amides, sulfoxonium ylides and silicon tethered directing groups for assisting transition metal catalyzed C-H functionalization reactions in the last decade.
引用
收藏
页码:12479 / 12521
页数:43
相关论文
共 175 条
[1]   Recent applications of C-H functionalization in complex natural product synthesis [J].
Abrams, Dylan J. ;
Provencher, Philip A. ;
Sorensen, Erik J. .
CHEMICAL SOCIETY REVIEWS, 2018, 47 (23) :8925-8967
[2]   Palladium-Catalyzed Template Directed C-5 Selective Olefination of Thiazoles [J].
Achar, Tapas Kumar ;
Biswas, Jyoti Prasad ;
Porey, Sandip ;
Pal, Tapas ;
Ramakrishna, Kankanala ;
Maiti, Siddhartha ;
Maiti, Debabrata .
JOURNAL OF ORGANIC CHEMISTRY, 2019, 84 (12) :8315-8321
[3]   Palladium-Catalyzed Directed meta-Selective C-H Allylation of Arenes: Unactivated Internal Olefins as Allyl Surrogates [J].
Achar, Tapas Kumar ;
Zhang, Xinglong ;
Mondal, Rahul ;
Shanavas, M. S. ;
Maiti, Siddhartha ;
Maity, Sabyasachi ;
Pal, Nityananda ;
Paton, Robert S. ;
Maiti, Debabrata .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2019, 58 (30) :10353-10360
[4]   Regiocontrolled Remote C-H Olefination of Small Heterocycles [J].
Achar, Tapas Kumar ;
Ramakrishna, Kankanala ;
Pal, Tapas ;
Porey, Sandip ;
Dolui, Pravas ;
Biswas, Jyoti Prasad ;
Maiti, Debabrata .
CHEMISTRY-A EUROPEAN JOURNAL, 2018, 24 (68) :17906-17910
[5]   Transition-Metal-Catalyzed Direct Arylation of (Hetero)Arenes by C-H Bond Cleavage [J].
Ackermann, Lutz ;
Vicente, Ruben ;
Kapdi, Anant R. .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2009, 48 (52) :9792-9826
[6]   Orthogonal Selectivity in C-H Olefination: Synthesis of Branched Vinylarene with Unactivated Aliphatic Substitution [J].
Agasti, Soumitra ;
Mondal, Bhaskar ;
Achar, Tapas Kumar ;
Sinha, Soumya Kumar ;
Suseelan, Anjana Sarala ;
Szabo, Kalman J. ;
Schoenebeck, Franziska ;
Maiti, Debabrata .
ACS CATALYSIS, 2019, 9 (10) :9606-9613
[7]   Palladium-catalyzed benzofuran and indole synthesis by multiple C-H functionalizations [J].
Agasti, Soumitra ;
Dey, Aniruddha ;
Maiti, Debabrata .
CHEMICAL COMMUNICATIONS, 2017, 53 (49) :6544-6556
[8]   Traceless directing group mediated branched selective alkenylation of unbiased arenes [J].
Agasti, Soumitra ;
Dey, Aniruddha ;
Maiti, Debabrata .
CHEMICAL COMMUNICATIONS, 2016, 52 (82) :12191-12194
[9]   Palladium-Catalyzed Synthesis of 2,3-Disubstituted Benzofurans: An Approach Towards the Synthesis of Deuterium Labeled Compounds [J].
Agasti, Soumitra ;
Maity, Soham ;
Szabo, Kalman J. ;
Maiti, Debabrata .
ADVANCED SYNTHESIS & CATALYSIS, 2015, 357 (10) :2331-2338
[10]   Orthogonal selectivity with cinnamic acids in 3-substituted benzofuran synthesis through C-H olefination of phenols [J].
Agasti, Soumitra ;
Sharma, Upendra ;
Naveen, Togati ;
Maiti, Debabrata .
CHEMICAL COMMUNICATIONS, 2015, 51 (25) :5375-5378