Transition metal catalysed cascade C-C and C-O bond forming events of alkynes

被引:3
作者
Barik, Padmanava [1 ]
Behera, Subhra Sriharsa [1 ]
Nayak, Laxmi Kanta [1 ]
Nanda, Laxmi Narayan [2 ]
Nanda, Santosh Kumar [1 ]
Patri, Padmanava [1 ]
机构
[1] Bhadrak Autonomous Coll, PG Dept Chem, Bhadrak 756100, Odisha, India
[2] Govt Autonomous Coll, PG Dept Chem, Anugul, Odisha, India
关键词
ALPHA-PYRONES; (Z)-4'-ACETOXY-2'-BUTENYL 2-ALKYNOATES; REGIOSELECTIVE SYNTHESIS; CYCLIZATION REACTION; EFFICIENT SYNTHESIS; TANDEM CYCLIZATION; REARRANGEMENT; ACETOXYPALLADATION; CARBOALKOXYLATION; ROUTE;
D O I
10.1039/d3ob02044d
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The past few decades have witnessed the emergence of domino reactions as a powerful tool for the multi-functionalization of alkynes for the rapid and smooth construction of complex molecular architectures. In this context, employing transition metal catalysis, vicinal/geminal cascade functionalization of alkynes involving C-C and C-O bond-formation reactions, has become a preferred strategy for the synthesis of oxygenated motifs. Despite this significant progress, reviews documenting such strategies are either metal/functional group-centric or target-oriented, thus hampering further developments. Therefore, in this review, different conceptual approaches based on C-C and C-O bond-forming events of alkynes such as carboxygenation (C-C and C 00000000 00000000 00000000 00000000 11111111 00000000 11111111 00000000 00000000 00000000 O bond formation), carboalkoxylation (C-C and C-OR bond formation), and carboacetoxylation (C-C and C-OAc bond formations) are discussed, and examples from the literature from the last two decades are presented. Further, we have presented detailed insights into the mechanism of different transformations. 1,2/1,1-Difunctionalization of alkynes (cascade C-C and C-O bond formations) serves as one of the reliable methods for the synthesis of numerous chemical architectures.
引用
收藏
页码:5052 / 5086
页数:35
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