✦ LIBER ✦

Synthesis of α,α-dichloro-β-hydroxynitrile mediated by tri-n-butylstibine

✍ Scribed by Yao-Zeng Huang; Chen Chen; Yanchang Shen

Publisher: Elsevier Science
Year: 1988
Tongue: French
Weight: 128 KB
Volume: 29
Category: Article
ISSN: 0040-4039
DOI: 10.1016/s0040-4039(00)80735-2

No coin nor oath required. For personal study only.

✦ Synopsis

a,U-Dichloro-P-hydroxynitriles were conveniently synthesized by the reaction of trichloroacetonitrile with aldehydes mediated by tri-n-butylstibine in excellent yields.

C4,o+Dichloro-fi -hydroxynitrile is rather inaccessible.2 Burton and coworkers

📜 SIMILAR VOLUMES

A novel olefination of carbonyl compound

A novel olefination of carbonyl compounds with α-bromoacetic ester mediated by tri-n-butylstibine

✍ Yaozeng Huang; Yanchang Shen; Chen Chen 📂 Article 📅 1986 🏛 Elsevier Science 🌐 French ⚖ 106 KB

ChemInform Abstract: A Novel Synthesis o

ChemInform Abstract: A Novel Synthesis of α-Azidocinnamates, α-Azido-α,β-Unsaturated Ketones, and β-Azidostyrenes Mediated by Cerium(IV) Ammonium Nitrate.

✍ Vijay Nair; Tesmol G. George 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 33 KB 👁 1 views

Synthesis of D-threo-2,2-[37Cl2]dichloro

Synthesis of D-threo-2,2-[37Cl2]dichloro-N-[β-hydroxy-α-(hydroxymethyl)-4-nitrophenyl]acetamide ([37Cl2]chloramphenicol)

✍ Marjorie Jacquemijns; Johannus F. C. Stavenuiter; Gijsbert Zomer 📂 Article 📅 1989 🏛 John Wiley and Sons 🌐 French ⚖ 141 KB

Synthesis of azetidin-3-ones by heterocy

Synthesis of azetidin-3-ones by heterocyclization of α-cyclohexylamino-α′,Β′-epoxy ketones

✍ A. M. Zvonok; N. M. Kuz'menok; L. S. Stanishevskii 📂 Article 📅 1988 🏛 Springer US 🌐 English ⚖ 434 KB

Synthesis of 17α-tri-N-butylstannylvinyl

Synthesis of 17α-tri-N-butylstannylvinyl-11β-substituted estrones: Precursors for high affinity estrogenic radioligands

✍ R.N. Hanson; M. Ghoshal; C. Rosenthal; F. Murphy 📂 Article 📅 1989 🏛 John Wiley and Sons 🌐 French ⚖ 92 KB

Synthesis of β-substituted α-iodo cycloa

Synthesis of β-substituted α-iodo cycloalkanones by the CuI-mediated conjugate addition of Grignard reagents to α-iodo cycloalkenones

✍ Chin-Kang Sha; Chen-Tso Tseng; Wen-Sheng Chang 📂 Article 📅 2001 🏛 Elsevier Science 🌐 French ⚖ 71 KB

CuI-mediated conjugate addition of Grignard reagents to a-iodo cycloalkenones afforded b-substituted a-iodo cycloalkanones in good to excellent yields.