Organolithium-Mediated Conversion of β-Functionalized Aziridines into Alkynyl Amino Alcohols and Diamines.

New Route to Azaspirocycles via the Orga

New Route to Azaspirocycles via the Organolithium-Mediated Conversion of β-Alkoxy Aziridines into Cyclopentenyl Amines.

✍ Stephen P. Moore; Susannah C. Coote; Peter O'Brien; John Gilday 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 29 KB

## 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.

ChemInform Abstract: Unexpected Products

ChemInform Abstract: Unexpected Products from the Attempted Organolithium-Mediated Conversion of β-Methoxy Aziridines into Allylic Amines.

✍ Susannah C. Coote; Peter O'Brien 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 79 KB

ChemInform Abstract: Organolithium-Media

ChemInform Abstract: Organolithium-Mediated Conversion of β-Alkoxy Aziridines into Allylic Sulfonamides: Effect of the N-Sulfonyl Group and a Formal Synthesis of (.+-.)-Perhydrohistrionicotoxin.

✍ Susannah C. Coote; Stephen P. Moore; Peter O'Brien; Adrian C. Whitwood; John Gil 📂 Article 📅 2009 🏛 John Wiley and Sons ⚖ 55 KB

## 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 v

A Stereoselective Entry into Functionali

A Stereoselective Entry into Functionalized 1,2-Diamines by Zinc-Mediated Homologation of α-Amino Acids.

✍ Cam Thuy Hoang; Valerie Alezra; Regis Guillot; Cyrille Kouklovsky 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 52 KB

Efficient Regio- and Stereoselective Con

Efficient Regio- and Stereoselective Conversions of Oxiranes and Aziridines into β-(Nitrooxy)-Substituted Alcohols and Amines by Using Bismuth Nitrate

✍ Biswanath Das; Maddeboina Krishnaiah; Katta Venkateswarlu; Vtukuri Saidi Reddy 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 German ⚖ 69 KB

Oxiranes and aziridines efficiently undergo ring opening with bismuth nitrate at room temperature to furnish the corresponding b-(nitrooxy)-substituted alcohols and amines respectively. The conversions are highly regio-and stereoselective and afford the nitrooxy-compounds in excellent yields within

Novel Synthetic Methodologies. Part 106.

Novel Synthetic Methodologies. Part 106. Efficient Regio- and Stereoselective Conversions of Oxiranes and Aziridines into β-(Nitrooxy)-Substituted Alcohols and Amines by Using Bismuth Nitrate.

✍ Biswanath Das; Maddeboina Krishnaiah; Katta Venkateswarlu; Vtukuri Saidi Reddy 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 26 KB