Their Reactions (their + reaction)

Distribution by Scientific Domains


Selected Abstracts


ChemInform Abstract: Synthesis of Chiral Aziridines Through Decarboxylative Generation of Sulfur Ylides and Their Reaction with Chiral Sulfinyl Imines.

CHEMINFORM, Issue 49 2009
David C. Forbes
Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a "Full Text" option. The original article is trackable via the "References" option. [source]


Synthesis of N-Alkylated Derivatives of Pyrazolo[1,5-a]pyrimidine and Their Reaction with Methylamine.

CHEMINFORM, Issue 4 2003
G. G. Danagulyan
Abstract For Abstract see ChemInform Abstract in Full Text. [source]


ChemInform Abstract: Stereoselective Synthesis of Secondary Organozinc Reagents and Their Reaction with Heteroatomic Electrophiles.

CHEMINFORM, Issue 18 2001
Eike Hupe
Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a "Full Text" option. The original article is trackable via the "References" option. [source]


ChemInform Abstract: Synthesis of 2-Imino-7-methyl-2,3-dihydroimidazo[1,2-a]pyrimidin-5(1H)-ones and Their Reactions with Nucleophiles.

CHEMINFORM, Issue 5 2009
Virginija Jakubkiene
Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a "Full Text" option. The original article is trackable via the "References" option. [source]


Synthesis of 5-Bromomethylisoxazoles and Their Reactions with Secondary Amines.

CHEMINFORM, Issue 16 2006
A. G. Aliev
Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF. [source]


Synthesis and Tuberculostatic Activity of Methyl 3-Isonicotinoyldithiocarbazate and S,S,-Dimethyl Dithiocarbonate Isonicotinoylhydrazone, and Their Reactions with Amines and Hydrazines.

CHEMINFORM, Issue 15 2003
H. Foks
Abstract For Abstract see ChemInform Abstract in Full Text. [source]


ChemInform Abstract: Synthesis of Methyl p-Alkoxyphenylcarbamates and Some of Their Reactions.

CHEMINFORM, Issue 29 2002
A. V. Velikorodov
Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a "Full Text" option. The original article is trackable via the "References" option. [source]


ChemInform Abstract: Synthesis of 4-(N,N-Dimethylaminomethylene)-2-alkyl-2-oxazolin-5-ones via Vilsmeier Haack Reagent and Their Reactions with Various N- and O-Nucleophiles.

CHEMINFORM, Issue 19 2001
Ram S. Singh
Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a "Full Text" option. The original article is trackable via the "References" option. [source]


9,10-Diarylanthracenes as Molecular Switches: Syntheses, Properties, Isomerisations and Their Reactions with Singlet Oxygen

CHEMISTRY - A EUROPEAN JOURNAL, Issue 36 2008
Daniel Zehm
Abstract A series of 9,10-diarylanthracenes with various substituents at the ortho positions have been synthesised by palladium-catalysed cross-coupling reactions. Such compounds exhibit interesting physical properties and can be applied as molecular switches. Despite the high steric demand of the substituents, products were formed in moderate-to-good yields. In some cases, microwave conditions further improved yields. Bis-coupling afforded two isomers (syn and anti) that do not interconvert at room temperature. These products were easily separated and their relative stereochemistries were unequivocally assigned by NMR spectroscopy and X-ray analysis. The syn and anti isomers exhibit different physical properties (e.g., melting points and solubilities) and interconversion by rotation around the aryl,aryl axis commences at <100,C for fluoro-substituted diarylanthracenes and at >300,C for alkyl- or alkoxy-substituted diarylanthracenes. The reactions with singlet oxygen were studied separately and revealed different reactivities and reaction pathways. The yields and reactivities depend on the size and electronic nature of the substituents. The anti isomers form the same 9,10-endoperoxides as the syn species, occasionally accompanied by unexpected 1,4-endoperoxides as byproducts. Thermolysis of the endoperoxides exclusively yielded the syn isomers. The interesting rotation around the aryl,aryl axis allows the application of 9,10-diarylanthracenes as molecular switches, which are triggered by light and air under mild conditions. Finally, the oxygenation and thermolysis sequence provides a simple, synthetic access to a single stereoisomer (syn) from an unselective coupling step. [source]


Highly Efficient Synthesis of Stereodefined Multisubstituted 1,4-Dicyano- and 1-Cyano-1,3-butadienes and Their Reactions with Organolithium Reagents

CHEMISTRY - A EUROPEAN JOURNAL, Issue 22 2007
Congyang Wang Dr.
Abstract Stereodefined multisubstituted 1-cyano- and 1,4-dicyano-1,3-butadiene derivatives were obtained in excellent yields of the isolated product from their corresponding monohalo- and dihalobutadienes and CuCN. This reaction proceeded with high stereoselectivity and retention of the stereochemistry of the starting halobutadienes. A study of the utility of the thus-obtained 1-cyano- and 1,4-dicyano-1,3-butadiene derivatives was demonstrated by their reactions with organolithium reagents. 2H -Pyrrole or iminocyclopentadiene derivatives were formed in high yields from 1-cyano-4-halo-1,3-butadienes and organolithium reagents. When 1,4-dicyano-1,3-butadienes were treated with organolithium reagents followed by trapping with electrophiles, a tandem process took place to afford 2H -pyrrolyl nitriles in excellent yields. Reduction of 1,4-dicyano-1,3-butadiene derivatives with LiAlH4 showed novel reaction patterns relative to normal nitriles. [source]