✦ LIBER ✦

Preparation of Novel (Fluoroaryl)silanes and Their Applications in the Organoyttrium-Catalyzed Hydrosilylation of Alkenes and Oxidation to Alcohols

✍ Scribed by Molander, Gary A.; Corrette, Christopher P.

Book ID: 121418735
Publisher: American Chemical Society
Year: 1998
Tongue: English
Weight: 206 KB
Volume: 17
Category: Article
ISSN: 0276-7333
DOI: 10.1021/om980698d

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Preparation of Nove

ChemInform Abstract: Preparation of Novel (Fluoroaryl)silanes and Their Applications in the Organoyttrium-Catalyzed Hydrosilylation of Alkenes and Oxidation to Alcohols.

✍ Gary A. Molander; Christopher P. Corrette 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 39 KB 👁 1 views

Preparation of novel axially chiral NHC–

Preparation of novel axially chiral NHC–Pd(II) complexes and their application in oxidative kinetic resolution of secondary alcohols

✍ Shi-Jia Liu; Lian-jun Liu; Min Shi 📂 Article 📅 2009 🏛 John Wiley and Sons 🌐 English ⚖ 242 KB 👁 1 views

ChemInform Abstract: Preparation of Nove

ChemInform Abstract: Preparation of Novel Axially Chiral NHC—Pd(II) Complexes and Their Application in Oxidative Kinetic Resolution of Secondary Alcohols.

✍ Shi-Jia Liu; Lian-jun Liu; Min Shi 📂 Article 📅 2009 🏛 John Wiley and Sons ⚖ 34 KB 👁 1 views

Preparation of β-Keto-β-alkanoyloxyphosp

Preparation of β-Keto-β-alkanoyloxyphosphonates, Phosphine Oxides and Sulfides and Their Application to the Synthesis of Novel Phosphoryl- and Thiophosphorylpyrazoles

✍ Touil, Soufiane; Slimani, Hosni 📂 Article 📅 2012 🏛 Japan Institute of Heterocyclic Chemistry 🌐 English ⚖ 739 KB

Synthesis of Chiral Amino Alcohols Embod

Synthesis of Chiral Amino Alcohols Embodying the Bispidine Framework and Their Application as Ligands in Enantioselectively Catalyzed Additions to CO and CC Groups

✍ Jan Spieler; Oliver Huttenloch; Herbert Waldmann 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 358 KB 👁 2 views

Two generally applicable routes for the synthesis of chiral amino alcohols embodying the bispidine framework have been developed. In linear route A the bispidine framework is built up successively from chiral primary amines via intermediate formation of a piperidinone and a bispidinone. In convergen

A Flexible Route to Chiral 2- endo -Subs

A Flexible Route to Chiral 2- endo -Substituted 9-Oxabispidines and Their Application in the Enantioselective Oxidation of Secondary Alcohols

✍ Breuning, Matthias; Steiner, Melanie; Mehler, Christian; Paasche, Alexander; Hei 📂 Article 📅 2009 🏛 American Chemical Society 🌐 English ⚖ 154 KB