An enantioselective synthesis of spiro-oxindole-based 3,4-dihydropyrroles via a Michael/cyclization cascade of 3-aminooxindoles with 2-enoylpyridines.

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An enantioselective synthesis of spiro-oxindole-based 3,4-dihydropyrroles via a Michael/cyclization cascade of 3-aminooxindoles with 2-enoylpyridines.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

@zh

2017年学术文章

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2017年学术文章

@zh-hans

2017年学术文章

@zh-my

2017年学术文章

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2017年學術文章

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2017年學術文章

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name

An enantioselective synthesis ...... indoles with 2-enoylpyridines.

@en

An enantioselective synthesis ...... indoles with 2-enoylpyridines.

@nl

type

Item

label

An enantioselective synthesis ...... indoles with 2-enoylpyridines.

@en

An enantioselective synthesis ...... indoles with 2-enoylpyridines.

@nl

prefLabel

An enantioselective synthesis ...... indoles with 2-enoylpyridines.

@en

An enantioselective synthesis ...... indoles with 2-enoylpyridines.

@nl

P1476

An enantioselective synthesis ...... xindoles with 2-enoylpyridines

@en

P2093

Baodong Cui

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Changlun Yuan

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

Jing Shan

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

Lei Qin

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

Nanwei Wan

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

Yi Wang

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

Yongzheng Chen

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

Yu Chen

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

P2860

Isolation, structure elucidation, and biomimetic total synthesis of versicolamide B, and the isolation of antipodal (-)-stephacidin A and (+)-notoamide B from Aspergillus versicolor NRRL 35600.

Enantioselective methodologies for the synthesis of spiro compounds.

Recent advances in organocatalytic methods for the synthesis of disubstituted 2- and 3-indolinones.

Isatins as privileged molecules in design and synthesis of spiro-fused cyclic frameworks.

Design, synthesis and QSAR studies of dispiroindole derivatives as new antiproliferative agents.

Synthesis and QSAR study of novel cytotoxic spiro[3H-indole-3,2'(1'H)-pyrrolo[3,4-c]pyrrole]-2,3',5'(1H,2'aH,4'H)-triones.

Regioselective synthesis of dispiro[1H-indene-2,3'-pyrrolidine-2',3''-[3H]indole]-1,2''(1''H)-diones of potential anti-tumor properties.

Substituted spiro [2.3'] oxindolespiro [3.2″]-5,6-dimethoxy-indane-1″-one-pyrrolidine analogue as inhibitors of acetylcholinesterase.

Regiospecific synthesis and biological evaluation of spirooxindolopyrrolizidines via [3+2] cycloaddition of azomethine ylide.

Organocatalytic asymmetric multicomponent cascade reaction via 1,3-proton shift and [3+2] cycloaddition: an efficient strategy for the synthesis of oxindole derivatives.

P304

8518-8522

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P31

scholarly article

P356

10.1039/C7OB02138K

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P433

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

P478

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

P50

Wen-Yong Han

P577

2017-10-01T00:00:00Z

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P698

28956054

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P921

enantioselectivity