Utilisation of Home Laundry Effluent (HLE) as a catalyst for expeditious one-pot aqueous phase synthesis of highly functionalised 4-thiazolidinones.

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Utilisation of Home Laundry Effluent (HLE) as a catalyst for expeditious one-pot aqueous phase synthesis of highly functionalised 4-thiazolidinones.

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2013 nî lūn-bûn

@nan

2013年の論文

@ja

2013年論文

@yue

2013年論文

@zh-hant

2013年論文

@zh-hk

2013年論文

@zh-mo

2013年論文

@zh-tw

2013年论文

@wuu

2013年论文

@zh

2013年论文

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name

Utilisation of Home Laundry Ef ...... ctionalised 4-thiazolidinones.

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Utilisation of Home Laundry Effluent

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type

Item

label

Utilisation of Home Laundry Ef ...... ctionalised 4-thiazolidinones.

@en

Utilisation of Home Laundry Effluent

@nl

prefLabel

Utilisation of Home Laundry Ef ...... ctionalised 4-thiazolidinones.

@en

Utilisation of Home Laundry Effluent

@nl

P1476

Utilisation of Home Laundry Ef ...... ctionalised 4-thiazolidinones.

@en

P2093

Mukesh Kumar Kumawat

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Ramendra K Singh

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Udaya Pratap Singh

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P2860

Fragment-based design, docking, synthesis, biological evaluation and structure-activity relationships of 2-benzo/benzisothiazolimino-5-aryliden-4-thiazolidinones as cycloxygenase/lipoxygenase inhibitors.

Designed multiple ligands. An emerging drug discovery paradigm.

Recent developments and biological activities of thiazolidinone derivatives: a review.

Targeting HIV entry through interaction with envelope glycoprotein 120 (gp120): synthesis and antiviral evaluation of 1,3,5-triazines with aromatic amino acids.

Synthesis and anticancer activity of isatin-based pyrazolines and thiazolidines conjugates.

5-Alkylated thiazolidinones as follicle-stimulating hormone (FSH) receptor agonists.

2-(Aryl)-3-furan-2-ylmethyl-thiazolidin-4-ones as selective HIV-RT inhibitors.

Convenient synthesis of fused heterocyclic 1,3,5-triazines from some N-acyl imidates and heterocyclic amines as anticancer and antioxidant agents.

Efficient regioselective three-component domino synthesis of 3-(1,2,4-Triazol-5-yl)-1,3-thiazolidin-4-ones as potent antifungal and antituberculosis agents.

Design, facile synthesis, and antibacterial activity of hybrid 1,3,4-thiadiazole-1,3,5-triazine derivatives tethered via -S- bridge.

P2888

2193-1801-2-466

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466

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scholarly article

P356

10.1186/2193-1801-2-466

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P478

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P50

Hans Raj Bhat

P577

2013-09-16T00:00:00Z

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P5875

257250505

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1035106673

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24083113

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3786069

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