The Journal of Organic Chemistry

pubs3.acs.org | Jun 20, 2008

Original contributions reporting novel, important findings of fundamental research in all branches of the theory and practice of organic and bioorganic chemistry.

http://pubs3.acs.org/acs/journals/toc.page?incoden=joceah&indecade=0&involume=73&inissue=12

Synthesis of azoxabicyclo[3.3.1]nonanones based on diastereoselective reactions of 1,1-bis(trimethylsilyloxy)ketene acetals with isoquinolines and quinolines

www.rsc.org | Jun 12, 2008

Densely functionalized azoxabicyclo[3.3.1]nonanones were prepared based on the reaction of 1,1-bis(silyloxy)ketene acetals with isoquinolinium and quinolinium salts.

http://www.rsc.org/publishing/journals/OB/article.asp?doi=b804139c

Lewis Base Activation of Lewis Acids: Catalytic, Enantioselective Addition of Glycolate-Derived Silyl Ketene Acetals to Aldehydes

feeds.acs.org | May 28, 2008

Scott E. Denmark and Won-jin ChungWeb Release Date: Wed, 28 May 2008 00:00:00 EDT (Article) DOI: 10.1021/jo8006539<img

http://feeds.acs.org/~r/acs/joceah/~3/299631673/jo8006539.html

Natural materials show anti-cancer promise-04/01/1992-PCE

www.icis.com | Jan 4, 1992

Efforts to find a cure for cancer now encompass the development of naturally-derived therapies.

http://www.icis.com/Articles/1992/01/04/37555/natural-materials-show-anti-cancer-promise.html

Gelest, Inc- Synthetic Organic Chemistry

Silicon-Based Synthetic Reagents Gelest produces a large variety of Silicon-based synthetic agents, which are used for the selective transformation of functional groups in organic synthesis.

http://www.gelest.com/applications/SyntheticOrganicChemistry.asp

Organic Chemistry Newsletter

Organic Chemistry Newsletter Worldwide Vol. 1, No. 2 (August 2002) ----------------------------------------------------------------- Welcome to Issue 1.2 of "Organic Chemistry Newsletter Worldwide".

http://www.organicworldwide.net/newsletter/2002august.html

Index

www.elsevier.com

3.5.4. Additional method. Preparation of organyltellurium trichlorides and tribromides by the reaction of tetraorganyltin compounds with tellurium tetrachloride and tetrabromide 49 3.6. The products of the hydrolysis of aryl tellurium trihalides 50 3.7. Aryl tellurenyl halides 51

http://www.elsevier.com/framework_products/promis_misc/petragnanitoc.doc

McMaster Chemistry: Warkentin

Our recent work has been concentrated around the chemistry of carbenes, such as alkoxyamino-, dialkoxy-, alkoxyaryloxy-, diaryloxy- and dialkylcarbenes. In all cases we have generated them from oxadiazoline precursors, by thermolysis or photolysis in solution, as depicted in Scheme 1, below.

http://www.chemistry.mcmaster.ca/faculty/warkentin/