A synthesis of fused acenaphthopyrrolizines via the 1,3-dipolar cycloaddition reaction of azomethine ylides with acetylenic esters.

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A synthesis of fused acenaphthopyrrolizines via the 1,3-dipolar cycloaddition reaction of azomethine ylides with acetylenic esters.

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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

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2017年学术文章

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2017年学术文章

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2017年学术文章

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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

A synthesis of fused acenaphth ...... ylides with acetylenic esters.

@en

A synthesis of fused acenaphth ...... ylides with acetylenic esters.

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type

Item

label

A synthesis of fused acenaphth ...... ylides with acetylenic esters.

@en

A synthesis of fused acenaphth ...... ylides with acetylenic esters.

@nl

prefLabel

A synthesis of fused acenaphth ...... ylides with acetylenic esters.

@en

A synthesis of fused acenaphth ...... ylides with acetylenic esters.

@nl

P1476

A synthesis of fused acenaphth ...... ylides with acetylenic esters.

@en

P2093

Issa Yavari

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Leila Baoosi

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Mohammad R Halvagar

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P2860

A short history of SHELX

Regio- and Stereoselective Synthesis of Spiropyrrolizidines and Piperazines through Azomethine Ylide Cycloaddition Reaction.

Synthesis of novel spirooxindolo-pyrrolidines, pyrrolizidines, and pyrrolothiazoles via a regioselective three-component [3+2] cycloaddition and their preliminary antimicrobial evaluation.

Enantioselective copper-catalyzed 1,3-dipolar cycloadditions.

The molecular diversity scope of 1,3-indandione in organic synthesis.

Molecular diversity of spirooxindoles. Synthesis and biological activity.

Synthesis of first ever 4-quinolone-3-carboxylic acid-appended spirooxindole-pyrrolidine derivatives and their biological applications.

Chemistry of withaferin-A: chemo, regio, and stereoselective synthesis of novel spiro-pyrrolizidino-oxindole adducts of withaferin-A via one-pot three-component [3+2] azomethine ylide cycloaddition and their cytotoxicity evaluation.

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.

An atom economic synthesis and antitubercular evaluation of novel spiro-cyclohexanones.

P2888

s11030-016-9721-8

P304

257-263

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P31

scholarly article

P356

10.1007/S11030-016-9721-8

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P433

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

P478

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

P577

2017-01-13T00:00:00Z

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P698

28084603

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P921

cycloaddition