Optimization and multigram scalability of a catalytic enantioselective borylative migration for the synthesis of functionalized chiral piperidines.

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Optimization and multigram scalability of a catalytic enantioselective borylative migration for the synthesis of functionalized chiral piperidines.

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2016 nî lūn-bûn

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2016年の論文

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2016年学术文章

@wuu

2016年学术文章

@zh

2016年学术文章

@zh-cn

2016年学术文章

@zh-hans

2016年学术文章

@zh-my

2016年学术文章

@zh-sg

2016年學術文章

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2016年學術文章

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Optimization and multigram sca ...... tionalized chiral piperidines.

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Optimization and multigram sca ...... tionalized chiral piperidines.

@nl

type

Item

label

Optimization and multigram sca ...... tionalized chiral piperidines.

@en

Optimization and multigram sca ...... tionalized chiral piperidines.

@nl

prefLabel

Optimization and multigram sca ...... tionalized chiral piperidines.

@en

Optimization and multigram sca ...... tionalized chiral piperidines.

@nl

P1476

Optimization and multigram sca ...... tionalized chiral piperidines.

@en

P2093

Dennis G Hall

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You-Ri Kim

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P2860

Oxygenase-Catalyzed Desymmetrization ofN,N-Dialkyl-piperidine-4-carboxylic Acids

Total synthesis of the marine alkaloid (-)-lepadin B.

Synthesis of pharmaceutically active compounds containing a disubstituted piperidine framework.

Synthesis of pyridine and dihydropyridine derivatives by regio- and stereoselective addition to N-activated pyridines.

Rings in drugs.

Analysis of the structural diversity, substitution patterns, and frequency of nitrogen heterocycles among U.S. FDA approved pharmaceuticals.

Intramolecular Pd(II)-catalyzed aerobic oxidative amination of alkenes: synthesis of six-membered N-heterocycles.

Concise synthesis and antimalarial activity of all four mefloquine stereoisomers using a highly enantioselective catalytic borylative alkene isomerization.

Mild, rhodium-catalyzed intramolecular hydroamination of unactivated terminal and internal alkenes with primary and secondary amines.

Total synthesis of the marine alkaloids (-)-lepadins a, b, and c based on stereocontrolled intramolecular acylnitroso-Diels-Alder reaction.

P304

4739-4748

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P31

scholarly article

P356

10.1039/C6OB00685J

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P433

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

P478

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

P577

2016-05-04T00:00:00Z

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P698

27143333

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P921

enantioselectivity