Decarboxylative Annulation of α-Amino Acids with β-Ketoaldehydes.

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Decarboxylative Annulation of α-Amino Acids with β-Ketoaldehydes.

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2018 nî lūn-bûn

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2018年の論文

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年學術文章

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2018年學術文章

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Decarboxylative Annulation of α-Amino Acids with β-Ketoaldehydes.

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Decarboxylative Annulation of α-Amino Acids with β-Ketoaldehydes.

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Item

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Decarboxylative Annulation of α-Amino Acids with β-Ketoaldehydes.

@en

Decarboxylative Annulation of α-Amino Acids with β-Ketoaldehydes.

@nl

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Decarboxylative Annulation of α-Amino Acids with β-Ketoaldehydes.

@en

Decarboxylative Annulation of α-Amino Acids with β-Ketoaldehydes.

@nl

P1476

Decarboxylative Annulation of α-Amino Acids with β-Ketoaldehydes

@en

P2093

Anirudra Paul

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N R Thimmegowda

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Thiago Galani Cruz

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P2860

Total synthesis of bryostatin 7 via C-C bond-forming hydrogenation

Novel dipolarophiles and dipoles in the metal-catalyzed enantioselective 1,3-dipolar cycloaddition of azomethine ylides

A cascade reaction with iminium ion isomerization as the key step leading to tetrahydropyrimido[4,5-d]pyrimidines.

Asymmetric Redox-Annulation of Cyclic Amines.

Enantioselective copper-catalyzed 1,3-dipolar cycloadditions.

Decarboxylative coupling reactions: a modern strategy for C-C-bond formation.

Recent advances in the catalytic asymmetric 1,3-dipolar cycloaddition of azomethine ylides.

The azomethine ylide route to amine C-H functionalization: redox-versions of classic reactions and a pathway to new transformations.

Redox-Annulation of Cyclic Amines and β-Ketoaldehydes.

Decarboxylation as the Key Step in C-C Bond-Forming Reactions.

P304

602-604

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P31

scholarly article

P356

10.1021/ACS.ORGLETT.7B03721

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P407

English

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P50

Daniel Seidel

P577

2018-01-12T00:00:00Z

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P698

29328663

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P932

5937137

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