Cobalt(II)porphyrin-Mediated Selective Synthesis of 1,5-Diketones via an Interrupted-Borrowing Hydrogen Strategy Using Methanol as a C1 Source

被引:18
作者
Biswal, Priyabrata [1 ]
Samser, Shaikh [1 ]
Nayak, Prakash [1 ]
Chandrasekhar, Vadapalli [2 ,3 ]
Venkatasubbaiah, Krishnan [1 ]
机构
[1] Natl Inst Sci Educ & Res NISER, Sch Chem Sci, Bhubaneswar 752050, Odisha, India
[2] Tata Inst Fundamental Res Hyderabad, Hyderabad 500046, Telangana, India
[3] Indian Inst Technol Kanpur, Dept Chem, Kanpur 208016, Uttar Pradesh, India
关键词
ONE-POT SYNTHESIS; CONJUGATE ADDITION; ALPHA-METHYLATION; KETONES; ALCOHOLS; AMINES; SESQUITERPENOIDS; ALKYLATION; REACTIVITY; EFFICIENT;
D O I
10.1021/acs.joc.1c00476
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A novel cobalt(II)porphyrin-mediated acceptorless dehydrogenation of methanol is reported for the first time. This methodology has been applied for the coupling of a variety of ketones with methanol to produce 1,5-diketones along with H-2 and H2O as the environment friendly byproducts. This paradigm was also demonstrated for a one-pot synthesis of substituted pyridines using a sequential addition protocol where the 1,5-diketones were generated in situ. From many experiments including those involving deuterium labeling, it is proposed that protonated cobalt(II)-porphyrin methoxide complex acts as an intermediate to generate formaldehyde along with a metal hydride.
引用
收藏
页码:6744 / 6754
页数:11
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