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Novel Syntheses of Nitrogen Heterocycles from Isocyanides

-15% su kodu: ENG15
97,74 
Įprasta kaina: 114,99 
-15% su kodu: ENG15
Kupono kodas: ENG15
Akcija baigiasi: 2025-03-03
-15% su kodu: ENG15
97,74 
Įprasta kaina: 114,99 
-15% su kodu: ENG15
Kupono kodas: ENG15
Akcija baigiasi: 2025-03-03
-15% su kodu: ENG15
2025-02-28 114.9900 InStock
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Knygos aprašymas

The direct copper(I)-catalyzed synthesis of oligosubstituted pyrroles from substituted methyl isocyanides and acceptor-substituted acetylenes as well as copper(I)-mediated route to pyrroles from substituted methyl isocyanides and non-activated terminal acetylenes have been investigated. 2-Substituted phenyl isocyanides were obtained by trapping of generated in situ ortho-lithiophenyl isocyanide with electrophiles. This strategy has been effectively employed for the new synthesis of substituted 3H-quinazolin-4-ones (-thiones) including the naturally occurring alkaloids deoxyvasicinone and tryptanthrine. The reactions of ortho-lithiophenyl isocyanide and other ortho-lithiohetaryl isocyanides with aldehydes, ketones, and carbon dioxide have been investigated in detail. Two novel rearrangements of the intermediate 2-lithio-4H-3,1-benzoxazines have been disclosed. A novel copper-catalyzed synthesis of benzimidazoles from ortho-bromoaryl isocyanides and primary amines has been developed.

Informacija

Autorius: Alexander Lygin
Leidėjas: Südwestdeutscher Verlag für Hochschulschriften AG Co. KG
Išleidimo metai: 2015
Knygos puslapių skaičius: 200
ISBN-10: 3838117549
ISBN-13: 9783838117546
Formatas: 220 x 150 x 13 mm. Knyga minkštu viršeliu
Kalba: Anglų

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