Facile access to functionalized indenes and fused quinolines by regioselective 5-enolexo-dig Michael addition and cyclization reactions.

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Facile access to functionalized indenes and fused quinolines by regioselective 5-enolexo-dig Michael addition and cyclization reactions.

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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

@zh-cn

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

Facile access to functionalize ...... ion and cyclization reactions.

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Facile access to functionalize ...... ion and cyclization reactions.

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type

Item

label

Facile access to functionalize ...... ion and cyclization reactions.

@en

Facile access to functionalize ...... ion and cyclization reactions.

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prefLabel

Facile access to functionalize ...... ion and cyclization reactions.

@en

Facile access to functionalize ...... ion and cyclization reactions.

@nl

P1476

Facile access to functionalize ...... ion and cyclization reactions.

@en

P2093

Sandeep K Ginotra

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Tohasib Yusub Chaudhari

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Vibha Tandon

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P2860

Rules for ring closure: application to intramolecular aldol condensations in polyketonic substrates

Rules for Anionic and Radical Ring Closure of Alkynes

Cyclizations of Alkynes: Revisiting Baldwin’s Rules for Ring Closure

DoMCoSAR: a novel approach for establishing the docking mode that is consistent with the structure-activity relationship. Application to HIV-1 protease inhibitors and VEGF receptor tyrosine kinase inhibitors.

Ionic liquid-promoted regiospecific Friedlander annulation: novel synthesis of quinolines and fused polycyclic quinolines.

Cyclooxygenase-1-selective inhibitors based on the (E)-2'-des-methyl-sulindac sulfide scaffold.

Transition-metal-catalyzed addition of heteroatom-hydrogen bonds to alkynes.

Recent Advances in the Synthesis of Indanes and Indenes.

Developments toward the synthesis and application of 3-hydroxyindanones.

Design, synthesis and evaluation of acridine and fused-quinoline derivatives as potential anti-tuberculosis agents.

P304

9319-9330

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P31

scholarly article

P356

10.1039/C7OB02498C

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P433

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

P478

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

P577

2017-10-31T00:00:00Z

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P698

29085944

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