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Chemistry > Chemical Synthesis > Learning Center > ChemNews > 2009 > September 2009
 
      Hot News  |  Latest ChemBlogs  |  New Literature  |   New Products  |  Product Spotlight September 2009

Welcome to ChemNews!

Our September ChemNews showcases our brand NEW and innovative Reagents for Selective Metalation and Deprotonation, catalysts, and building blocks for Chemical Synthesis. In addition, we're featuring the latest literature for chemical synthesis available from Sigma-Aldrich, as well our latest product highlights — all easily accessed from one convenient location.

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Latest ChemBlogs


 Pd-Catalyzed Benzylation of Heteroarenes

Fagnou and coworkers reported a Pd-catalyzed benzylation reaction of a variety of aromatic heterocycles, including thiazoles, thiophenes, indolizines, imidazopyrimidines, triazoles, oxazoles, and furans. Traditional methods for this transformation involve either Friedel-Crafts alkylation (requires strong Lewis or Bronsted acids and invariably precludes use of electron-deficient substrates) or deprotonation and addition of an electrophile (in both methods protection of acid- and base-sensitive functionalities is necessary, respectively). 
Read More...

Pd-Catalyzed Benzylation of Heteroarenes



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New Literature

Aldrichimica Acta
Aldrichimica Acta Volume 42, No. 1
Vol. 42, No. 1 Dedicated to Dr. Alfred Bader on the Occasion of His 85th Birthday
(3.32 Mb PDF) 
  ChemFiles
ChemFiles Volume 9, No. 4
Vol. 9, No. 4
Microreactor Technology

(2.71 Mb PDF)
  ChemFiles
ChemFiles Volume 9, No. 3
Vol. 9, No. 3
Chiral Building Blocks

(1.6 Mb PDF)

 

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New Products
                     

NEW Reagents for Selective Metalation from Chemetall

 Chemetall

 
656984 Structure

656984
1.3 M in tetrahydrofuran
703486 Structure

703486
1.2 M in tetrahydrofuran
703540 Structure

703540
1.0 M in tetrahydrofuran/toluene
 
703559 Structure

703559
 Selective 1,2-Additons
703583 Structure

703583
3.2 M in 2-methyltetrahydrofuran
703591 Structure

703591
3.4 M in 2-methyltetrahydrofuran
 
703575 Structure

703575
2.9 M in 2-methyltetrahydrofuran
703494 Structure

703494
2.2 M in heptane
703567 Structure

703567
2.9 M in 2-methyltetrahydrofuran
 
The Lithium Company

                     

NEW Heterocycles

 
 
688584 Structure

688584
706817 Structure

706817
708135 Structure

708135
 
706485 Structure

706485
708402 Structure

708402
710822 Structure

710822
 

                     

NEW Catalysts

 
 
704946 Structure

704946

704954 Structure

704954


708739

Buchwald palladacyclic catalysts for amination
 
701475 Structure

701475
701785 Structure

701785
708674 Structure

708674
701823 Structure

701823
Catalyst for deprotection of N-allyl amides and lactams Hydroacylation catalyst Transfer Hydrogenation catalysts
 
701572 Structure

701572

701793 Structure

701793
701815 Structure

701815

Enantioselective hydrogenation catalysts
 
705764 Structure

705764
705772 Structure

705772
Catalysts for Mannich-type transformation
 
705780 Structure

705780
705799 Structure

705799
Catalysts for Mannich-type transformation
 
674125 Structure

674125

Catalyst for Suzuki Coupling under air
704881 Structure

704881
Catalyst for nucleophilic addition to alkynes
708933 Structure

708933

Cross-coupling Ligand
 

 

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Product Spotlight

Super Silyl Protecting Groups – Unique Reactivity in C–C Bond Forming Reactions
Super Silyl Protecting Groups

 

α-Bromo Amides–Use in Asymmetric Nickel-Catalyzed Negishi Couplings
α-Bromo Amides–Use in Asymmetric Nickel-Catalyzed Negishi Couplings

 

DIH – Highly efficient and economical reagent for Iodination
DIH Tech Spotlight

 
 

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