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Mild Protocol (mild + protocol)

Distribution by Scientific Domains
Chemistry100%

Selected Abstracts

ChemInform Abstract: A Mild Protocol for the Efficient Synthesis of 5,6-Unsubstituted 1,4-Dihydropyridines.

CHEMINFORM, Issue 3 2010
Swarupananda Maiti
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]

A Mild Protocol for the Deoxygenation of ,-Hydrogen-Containing Sulfoxides to the Corresponding Sulfides.

CHEMINFORM, Issue 41 2004
Gurpreet S. Bhatia
Abstract For Abstract see ChemInform Abstract in Full Text. [source]

A Mild Protocol for Allylation and Highly Diastereoselective syn or anti Crotylation of Aldehydes in Biphasic and Aqueous Media Utilizing Potassium Allyl- and Crotyltrifluoroborates.

CHEMINFORM, Issue 12 2003
Avinash N. Thadani
Abstract For Abstract see ChemInform Abstract in Full Text. [source]

Mild Protocols for Generating Molecular Complexity: A Comparative Study of Hetero-Domino Reactions Based on the Oxidant and the Substitution Pattern.

CHEMINFORM, Issue 24 2005
Jose I. Candela Lena
Abstract For Abstract see ChemInform Abstract in Full Text. [source]

An Organocatalytic Synthesis of cis-N -Alkyl- and N -Arylaziridine Carboxylates

ADVANCED SYNTHESIS & CATALYSIS (PREVIOUSLY: JOURNAL FUER PRAKTISCHE CHEMIE), Issue 16 2009

Abstract An extremely mild protocol that employs readily available starting materials, i.e., aldehyde, amine and alkyl diazoacetate, returns structurally diverse N -substituted-C-2/3-difunctionalised aziridines in excellent yields and stereoselectivities when pyridinium triflate is incorporated as an organocatalyst. The reaction process is environmentally benign affording water and nitrogen as the only by-products. This racemic protocol paves the way for the development of novel asymmetric organocatalysts capable of generating optically active aziridines. [source]