乙酰丙酮镍(II)

Fieser and Fieser's Reagents for Organic Synthesis Pub Date : 2017-02-21 DOI:10.1002/9780471264194.FOS11349

T. Ho, M. Fieser, L. Fieser

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摘要

这篇文章没有摘要。关键词:dieles - alder反应;C-Alkylation;1、8-diarylnaphthalenes;邻氨基甲酸芳酯和三氟甲酸芳酯与RMgCl的偶联β-enamino内酯;carbozincation;联苯;1,2-syn炔烃加成;homocouplings;他们;共轭增加;[4 + 2]环加成;交叉耦合;羰基化合物的有机金属反应;addition-coupling序列;他们;N-arylation;homoallylation;[2 + 2 + 2]环加成;1、4-silaboration;烷基化;(E) -allylsilanes;耦合反应;hydrophosphinylation;耦合;耦合;还原迈克尔加法;亚胺的还原;耦合;n-arylation;除了

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Nickel(II) acetylacetonate

This article has no abstract. Keywords: diels–alder reactions; C-Alkylation; 1,8-diarylnaphthalenes; coupling of aryl O-carbamates and aryl triflates with RMgCl; β-enamino lactones; carbozincation; biphenyls; 1,2-syn addition to alkynes; homocouplings; cross-couplings; conjugate additions; [4 + 2]cycloaddition; cross couplings; organometallic reactions of carbonyl compounds; addition-coupling sequences; cross-couplings; N-arylation; homoallylation; [2 + 2 + 2]cycloaddition; 1,4-silaboration; alkylations; (E)-allylsilanes; coupling reactions; hydrophosphinylation; coupling; Coupling; reductive michael addition; reduction of imines; coupling; n-arylation; addition

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Fieser and Fieser's Reagents for Organic Synthesis

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