✦ LIBER ✦

A Totally Radical Approach to the Control of Stereochemistry: Coupling of Prochiral Radicals with Chiral Nitroxyl Radicals

✍ Scribed by Prof. Rebecca Braslau; Leland C. Burrill; Lara K. Mahal; Todd Wedeking

Publisher: John Wiley and Sons
Year: 1997
Tongue: English
Weight: 244 KB
Volume: 36
Category: Article
ISSN: 0044-8249
DOI: 10.1002/anie.199702371

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: A Total Radical App

ChemInform Abstract: A Total Radical Approach to the Control of Stereochemistry: Coupling of Prochiral Radicals with Chiral Nitroxyl Radicals.

✍ R. BRASLAU; L. C. II BURRILL; L. K. MAHAL; T. WEDEKING 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 31 KB 👁 1 views

Stereochemical Studies of Chiral Acyclic

Stereochemical Studies of Chiral Acyclic Nitroxides Coupling with a Prochiral Radical.

✍ Rebecca Braslau; Vladimir Chaplinski; Aaron Nilsen; Navamoney Arulsamy 📂 Article 📅 2004 🏛 John Wiley and Sons ⚖ 15 KB

ChemInform Abstract: Stereoselective Cou

ChemInform Abstract: Stereoselective Coupling of Prochiral Radicals with a Chiral C2-Symmetric Nitroxide.

✍ Rebecca Braslau; Neeta Naik; Hendrik Zipse 📂 Article 📅 2000 🏛 John Wiley and Sons ⚖ 39 KB 👁 1 views

ChemInform Abstract: Oxidative Coupling

ChemInform Abstract: Oxidative Coupling of Alkynes Mediated by Nitroxyl Radicals under Sonogashira Conditions and Pd-Free Catalytic Approach to Stable Radicals of 3-Imidazoline Family with Triple Bonds.

✍ Sergei F. Vasilevsky; Olga L. Krivenko; Igor V. Alabugin 📂 Article 📅 2008 🏛 John Wiley and Sons ⚖ 31 KB

Enantioselective Allylation of the α-Sul

Enantioselective Allylation of the α-Sulfonyl Radical Controlled by Coordination of a Chiral Lewis Acid to an Enantiotopic Sulfonyl Oxygen.

✍ Yoshihiko Watanabe; Nobuyuki Mase; Ryuji Furue; Takeshi Toru 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 32 KB 👁 1 views

ChemInform Abstract: Double Diastereosel

ChemInform Abstract: Double Diastereoselection in Intramolecular Photocycloadditions: A Radical Rearrangement Approach to the Total Synthesis of the Spirovetivane Phytoalexin (.+-.)-Lubiminol.

✍ M. T. CRIMMINS; Z. WANG; L. A. MCKERLIE 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 41 KB 👁 1 views

## Double Diastereoselection in Intramolecular Photocycloadditions: A Radical Rearrangement Approach to the Total Synthesis of the Spirovetivane Phytoalexin (±)-Lubiminol. -Key steps in the synthesis of the title compound (XIII) are a conjugate addition-cyclization reaction to prepare compound (I