✦ LIBER ✦

ChemInform Abstract: Reductive Cleavage of the Se—Se Bond by the Sm—Me3SiCl—H2O System: Preparation of Unsymmetrical Phenyl Selenides.

✍ Scribed by Lei Wang; Yongmin Zhang

Publisher: John Wiley and Sons
Year: 2010
Weight: 32 KB
Volume: 30
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.199915202

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Reductive Cleavage of Se—Se Bond by Sm/N

Reductive Cleavage of Se—Se Bond by Sm/NiCl2 or Sm/NiCl2×6H2O System: A Novel Preparation of Unsymmetrical Aryl Selenides.

✍ R. E. Chen; W. K. Su 📂 Article 📅 2006 🏛 John Wiley and Sons ⚖ 15 KB 👁 1 views

A Novel Synthesis of Unsymmetrical Selen

A Novel Synthesis of Unsymmetrical Selenides via the Cleavage of Se—Se Bond by Sm/cat.CoCl2 System.

✍ Rener Chen; Weike Su; Weihui Zhong 📂 Article 📅 2006 🏛 John Wiley and Sons ⚖ 14 KB 👁 1 views

ChemInform Abstract: Reductive Cleavage

ChemInform Abstract: Reductive Cleavage of the Se—Se Bond in Diselenides by the Sm/HgCl2 System: Formation and Reactions of Samarium Selenolates.

✍ Lei Wang; Yongmin Zhang 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 36 KB 👁 2 views

ChemInform Abstract: Reductive Cleavage

ChemInform Abstract: Reductive Cleavage of the Se—Se Bond by the Sm/CrCl3 System: A Novel One-Pot Method for the Synthesis of Selenoesters.

✍ Yunkui Liu; Yongmin Zhang 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 30 KB 👁 2 views

ChemInform Abstract: Reductive Cleavage

ChemInform Abstract: Reductive Cleavage of the Se—Si Bond in Arylselenotrimethylsilanes: Novel Method for the Synthesis of Unsymmetrical Selenides.

✍ Songlin Zhang; Yongmin Zhang 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 27 KB 👁 2 views

Reductive cleavage of the Se–Se bond in

Reductive cleavage of the Se–Se bond in diselenides by the Sm/HgCl2 system: Formation and reactions of samarium selenolates

✍ Lei Wang; Yongmin Zhang 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 137 KB 👁 2 views

Treatment of diaryl diselenides and dialkyl diselenides with metallic samarium and mercury (II) chloride in tetrahydrofuran conveniently gave samarium arylselenolates and alkylselenolates. These "living" species reacted with acyl chlorides, acid anhydrides, methyl chloroformate, organic halides, epo