Friday 24 June 2016

Lewis Acid Triggered Regioselective Magnesiation and Zincation of Uracils, Uridines, and Cytidines

 

Abstract Image


The Lewis acid MgCl2 allows control of the metalation regioselectivity of uracils and uridines. In the absence of the Lewis acid, metalation of uracil and uridine derivatives with TMPMgCl·LiCl occurs at the position C(5). In the presence of MgCl2, zincation using TMP2Zn·2LiCl·2MgCl2 occurs at the position C(6). This metalation method provides easy access to functionalized uracils and uridines. Using TMP2Zn·2LiCl·2MgCl2 also allows to functionalize cytidine derivatives at the position C(6).



The selective functionalization of uridines is an important synthetic goal because of the biological relevance of many substituted uridines. They are known to display antibiotic, antifungal, anticancer, and antiviral activity. Knochel and co-workers at Ludwig-Maximilians-Universität extended their investigation of metalation of heterocyclic systems to uridines. They reported the regioselective metalation of uridines at the C(5) or C(6) position and the subsequent functionalization of these metalated nucleoside derivatives with electrophiles ( Org. Lett. 2016, 18, 1068). Metalation of a protected uridine (A) with a slight excess of TMPMgCl·LiCl afforded the C(5) magnesiated uridine (C(5):C(6) = 98:2) in quantitative yield. The presence of MgCl2 inversed the regioselectivity of the metalation. Zincation of a protected uridine (A) with 1.2 equiv of TMP2Zn·2LiCl·2MgCl2 produced the C(6) bis-zincated uridine (C(5):C(6) = 3:97) also in quantitative yield. The C(5) or C(6) metalated uridines were then functionalized with a variety of electrophiles. This chemistry was successfully extended to the regioselective C6 metalation and functionalization of cytidines. The deprotection of the substituted uridines and cytidines afforded the corresponding functionalized nucleosides.

      

Lewis Acid Triggered Regioselective Magnesiation and Zincation of Uracils, Uridines, and Cytidines

Department Chemie, Ludwig-Maximilians-Universität, Butenandtstrasse 5-13, 81377 München, Germany
Org. Lett., 2016, 18 (5), pp 1068–1071
DOI: 10.1021/acs.orglett.6b00190

 
 
 
 
 
 
 
 
 
 
////////////////Lewis Acid,  Regioselective Magnesiation, Zincation, Uracils, Uridines, Cytidines

Tuesday 21 June 2016

Organocatalytic azomethine imine-olefin click reaction: high-yielding stereoselective synthesis of spiroindane-1,3-dione-pyrazolidinones

Graphical abstract: Organocatalytic azomethine imine-olefin click reaction: high-yielding stereoselective synthesis of spiroindane-1,3-dione-pyrazolidinones.
 In search of developing new useful “click reactions”, herein we report the organocatalytic azomethine imine-olefin [3 + 2]-cycloaddition as a new click reaction for the synthesis of drug-like spiroindane-1,3-dione-pyrazolidinones from indane-1,3-diones, aldehydes and N,N-cyclic azomethine imines through amino acid-catalysis. The scope of this new click reaction is demonstrated using many examples with high reactivity, selectivity and yields.




 




 
Happy to share with you our recent work on the development of Tomita zipper-cyclization (TZC) reaction…I am sure that this reaction may become useful tool for organic chemists in near future…


Paper

Organocatalytic azomethine imine-olefin click reaction: high-yielding stereoselective synthesis of spiroindane-1,3-dione-pyrazolidinones

*Corresponding authors
a
School of Chemistry, University of Hyderabad, Hyderabad-500 046, India
E-mail: ramsc@uohyd.ac.in
Fax: +91-40-23012460
Org. Biomol. Chem., 2016, Advance Article

DOI: 10.1039/C6OB01009A http://pubs.rsc.org/en/content/articlelanding/2016/ob/c6ob01009a#!divAbstract





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Tuesday 14 June 2016

An expeditious green route toward 2-aryl-4-phenyl-1H-imidazoles


https://static-content.springer.com/image/art%3A10.1186%2Fs13588-014-0009-7/MediaObjects/13588_2014_Article_9_Sch1_HTML.gif
Scheme 1
Ultrasound-assisted synthesis of 2-aryl-4-phenyl-1 H -imidazoles.

A rapid and simple synthetic procedure to synthesize diversely substituted 2-aryl-4-phenyl-1H-imidazoles has been reported. Other salient features of this protocol include milder conditions, atom-economy, easy extraction, and minimum wastes. The present procedure may find application in the synthesis of biologically active molecules.

 

An expeditious green route toward 2-aryl-4-phenyl-1H-imidazoles

  • Debasish BandyopadhyayEmail author,
  • Lauren C Smith,
  • Daniel R Garcia,
  • Ram N Yadav and
  • Bimal K BanikEmail author
Organic and Medicinal Chemistry Letters20144:9
DOI: 10.1186/s13588-014-0009-7

 

General procedure for the synthesis of 2-aryl-4-phenyl-1H-imidazoles

A solution of the aldehyde (1 mmol) and threefold excess of ammonium acetate (3 mmol) in methanol (2 mL) was placed in a B5510-DTH (Branson ultrasonic cleaner; Model-5510, frequency 42 KHz with an output power 135 Watts; Branson Ultrasonics, Danbury, CT, USA) sonicator at room temperature. The ultrasonic irradiation was started and a solution of phenylglyoxal monohydrate (1 mmol) in methanol (1 mL) was slowly added dropwise (by a syringe) to the above solution during a period of 15 min. The resulting mixture was continued to irradiate as specified in Table 1. After completion of the reaction (monitored by TLC with an interval of 5 min), the methanol was evaporated under reduced pressure and the crude mass was extracted with ethyl acetate (2 × 5 mL). The combined organic layer was washed with brine (10 mL) and water (10 mL) successively and dried over anhydrous sodium sulfate. The extract was then concentrated, and the crude product was purified using flash chromatography (neutral alumina, 1% triethylamine in methanol) to afford pure compounds.

 http://orgmedchemlett.springeropen.com/articles/10.1186/s13588-014-0009-7

////////////Imidazole,  Green chemistryUltrasoundHeterocyclesMedicinal chemistry , Azaheterocycles

Saturday 11 June 2016

Nickel-Catalyzed Cross-Coupling of Organolithium Reagents


During the past years, Feringa and co-workers have developed very efficient palladium-catalyzed methodologies for the cross-coupling of organolithium reagents. 
They have now described that nickel-based catalytic systems are also able to successfully cross-couple these organometallic reagents to a variety of (hetero)aryl electrophiles ( Chem. Eur. J. 2016, 22, 3991). 
The reactions take place in toluene at room temperature with a 50% molar excess of the organolithium reagent and are usually finished within an hour. 
In order to limit the formation of reduced (hetero)aryl electrophile, a different catalyst has to be used for the efficient coupling of aryl- or alkyl-lithium reagents, a N-heterocyclic carbene ligated one (C3 above) for the former and bis(diethyldiphosphino)ethane ligated one (C1 above) for the latter. 
While the substrate scope appears to be limited by the high reactivity of the organometallic partner, these nickel-catalyzed protocols allow a number of less usual electrophiles, such as methyl ethers or fluorides, to engage in the cross-coupling reaction.
 See original article

Homogeous Catalysis

Nickel-Catalyzed Cross-Coupling of Organolithium Reagents with (Hetero)Aryl Electrophiles (pages 3991–3995)Dorus Heijnen, Dr. Jean-Baptiste Gualtierotti, Dr. Valentín Hornillos and Prof. Dr. Ben L. Feringa
Version of Record online: 4 FEB 2016 | DOI: 10.1002/chem.201505106
Thumbnail image of graphical abstract
Nickel-catalyzed cross-coupling of aromatic electrophiles with organolithium reagents is presented. The use of a commercially available nickel N-heterocyclic carbene complex allows reaction with a variety of (hetero)aryllithium compounds, whereas a commercially available electron-rich nickel bisphosphine complex smoothly converts alkyllithium species into the corresponding coupled product.





Thursday 9 June 2016

On-Water Synthesis of Biaryl Sulfonyl Fluorides

.
1H NMR



 Compounds containing a sulfur–fluoride bond are receiving escalating attention in both the chemical and the biological literature. The need to activate the S–F bond through formation of a hydrogen bond in the presence of a proximal nucleophile forms the basis for sulfonyl fluorides to be utilized as privileged biocompatible orthogonal electrophiles in biological systems. Arvidsson at the Karolinska Institute and his co-workers at the University of KwaZulu-Natal reported an efficient, ligand-free, and additive free Suzuki–Miyaura coupling that is compatible with an aromatic sulfonyl fluoride moiety ( J. Org. Chem. 2016, 81, 2618). After extensive optimization studies, mild reaction conditions were identified that minimized hydrolysis of the aromatic sulfonyl fluoride. Palladium acetate was the most effective catalyst, and utilization of triethylamine as the base afforded the highest yield. The reaction was conducted in water as solvent, at room temperature. These mild reaction conditions were compatible with a variety of functional groups on the boronic acid, including: nitro, chloro, fluoro, nitrile, and ethers. The desired biaryl sulfonyl fluorides were obtained in good-to-excellent yields.




19 F NMR












Abstract Image.




On-Water Synthesis of Biaryl Sulfonyl Fluorides

Catalysis and Peptide Research Unit, University of KwaZulu-Natal, Durban, 4041, South Africa
Science for Life Laboratory, Drug Discovery & Development Platform & Division of Translational Medicine and Chemical Biology, Department of Medical Biochemistry and Biophysics, Karolinska Institutet, SE-171 21 Stockholm, Sweden
J. Org. Chem., 2016, 81 (6), pp 2618–2623
DOI: 10.1021/acs.joc.5b02770


 http://pubs.acs.org/doi/abs/10.1021/acs.joc.5b02770




 GC MS


 HR MS



 

 


 







 Praveen Kumar
 Praveen Kumar
PhD
PostDoc Position

Research experience

  • May 2014–
    present
    PostDoc Position
    University of KwaZulu-Natal · School of Pharmacy and Pharmacology · Catalysis and Peptide Research Unit
    South Africa · Durabn
  • Jan 2009–
    Jan 2014
    SRF
    Indian Institute of Integrative Medicine · Bio-Organic Chemistry Division (IIIM) · Dr. S. Koul
    India · Jammu
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Start of the Euro 2016

Tuesday 7 June 2016

An efficient Passerini tetrazole reaction (PT-3CR)


Green Chem., 2016, Advance Article
DOI: 10.1039/C6GC00910G, Communication
Ajay L. Chandgude, Alexander Domling
A sonication accelerated, catalyst free, simple, high yielding and efficient method for the Passerini-type three-component reaction (PT-3CR) has been developed.


An efficient Passerini tetrazole reaction (PT-3CR)


see
http://pubs.rsc.org/en/Content/ArticleLanding/2016/GC/C6GC00910G?utm_source=feedburner&utm_medium=feed&utm_campaign=Feed%3A+rss%2FGC+%28RSC+-+Green+Chem.+latest+articles%29#!divAbstract

An efficient Passerini tetrazole reaction (PT-3CR)

*
Corresponding authors
a
Department of Drug Design, University of Groningen, Antonius Deusinglaan 1, 9713 AV Groningen, The Netherlands 
E-mail: a.s.s.domling@rug.nl
Web: http://www.drugdesign.nl/
Green Chem., 2016, Advance Article

DOI: 10.1039/C6GC00910G













 A sonication accelerated, catalyst free, simple, high yielding and efficient method for the Passerini-type three-component reaction (PT-3CR) has been developed. It comprises the reaction of an aldehyde/ketone, an isocyanide and a TMS-azide in methanol : water (1 : 1) as the solvent system. The use of sonication not only accelerated the rate of the reaction but also provided good to excellent quantitative yields. This reaction is applicable to a broad scope of aldehydes/ketones and isocyanides.














  
Ajay L. Chandgude







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