Michael Addition of Chiral Formaldehyde N,N-Dialkylhydrazones to Activated Cyclic Alkenes.

ChemInform Abstract: Asymmetric Michael

ChemInform Abstract: Asymmetric Michael Addition of Formaldehyde N,N-Dialkylhydrazones to Alkylidene Malonates.

✍ Juan Vazquez; Auxiliadora Prieto; Rosario Fernandez; Dieter Enders; Jose M. Lass 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 29 KB 👁 2 views

## 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 v

Stereoselective Michael Addition of Form

Stereoselective Michael Addition of Formaldehyde N,N-Dialkylhydrazones to α,β.-Unsaturated Carbonyl Compounds

✍ Elena Diez; Rosario Fernandez; Jose M. Lassaletta; Eloisa Martin-Zamora; Juan Va 📂 Article 📅 2006 🏛 John Wiley and Sons ⚖ 16 KB 👁 1 views

Organocatalytic Conjugate Addition of Fo

Organocatalytic Conjugate Addition of Formaldehyde N,N-Dialkylhydrazones to β,γ-Unsaturated α-Keto Esters.

✍ Raquel P. Herrera; David Monge; Eloisa Martin-Zamora; Rosario Fernandez; Jose M. 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 32 KB 👁 1 views

ChemInform Abstract: “On Water” Nucleoph

ChemInform Abstract: “On Water” Nucleophilic Addition of Formaldehyde N,N-Dialkylhydrazones to α-Keto Esters.

✍ Ana Crespo-Pena; Eloisa Martin-Zamora; Rosario Fernandez; Jose M. Lassaletta 📂 Article 📅 2011 🏛 John Wiley and Sons ⚖ 30 KB 👁 1 views

ChemInform Abstract: Stereoselective Syn

ChemInform Abstract: Stereoselective Synthesis of Trifluoromethylated Compounds: Nucleophilic Addition of Formaldehyde N,N-Dialkylhydrazones to Trifluoromethyl Ketones.

✍ Carmen Pareja; Eloisa Martin-Zamora; Rosario Fernandez; Jose M. Lassaletta 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 36 KB 👁 1 views

## 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 v

Imidyl radicals. 3. Stereoselectivity of

Imidyl radicals. 3. Stereoselectivity of radical additions of N-haloimides to cyclic alkenes

✍ André Kirsch; Ulrich Lüning; Oliver Krüger 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 66 KB 👁 1 views

N-Haloimides (1 -5) are used in two types of radical chain reactions: (i) the selective Ziegler bromination of allylic and benzylic positions [1], which are bromine atom chain reactions [2] and (ii) imidyl radical [3, 4] chain reactions like substitutions and especially additions to double bonds [5,