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Dearomatizing conversion of pyrazines to 1,4-dihydropyrazine derivatives via transition-metal-free diboration, silaboration, and hydroborationElectronic supplementary information (ESI) available: Experimental details and characterization data of the products. See DOI: 10.1039/c2cc34086k
Pyrazines and substituted pyrazines undergo addition of boron reagents having B-B, Si-B, and H-B bonds under transition-metal-free conditions, leading to high-yield synthesis of N -borylated 1,4-dihydropyrazines and 1,2,3,4-tetrahydropyrazine. Pyrazine undergoes addition of boron reagents having B-B...
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creator | Oshima, Kazuyuki Ohmura, Toshimichi Suginome, Michinori |
description | Pyrazines and substituted pyrazines undergo addition of boron reagents having B-B, Si-B, and H-B bonds under transition-metal-free conditions, leading to high-yield synthesis of
N
-borylated 1,4-dihydropyrazines and 1,2,3,4-tetrahydropyrazine.
Pyrazine undergoes addition of boron reagents having B-B, Si-B, and H-B bonds under transition-metal-free conditions. |
doi_str_mv | 10.1039/c2cc34086k |
format | article |
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N
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N
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N
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Pyrazine undergoes addition of boron reagents having B-B, Si-B, and H-B bonds under transition-metal-free conditions.</abstract><doi>10.1039/c2cc34086k</doi><tpages>3</tpages></addata></record> |
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source | Royal Society of Chemistry |
title | Dearomatizing conversion of pyrazines to 1,4-dihydropyrazine derivatives via transition-metal-free diboration, silaboration, and hydroborationElectronic supplementary information (ESI) available: Experimental details and characterization data of the products. See DOI: 10.1039/c2cc34086k |
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