✦ LIBER ✦

Fungicidal activity of esters of acyl- and vinylphosphonic acids

✍ Scribed by Zh. V. Molodykh; I. A. Aleksandrova; R. U. Belyalov; T. Kh. Gazizov; V. S. Reznik

Book ID: 112401790
Publisher: Springer
Year: 1990
Tongue: English
Weight: 328 KB
Volume: 24
Category: Article
ISSN: 0091-150X
DOI: 10.1007/bf00766865

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Fungicidal activity of tributyltin alkyl

Fungicidal activity of tributyltin alkylsulfate esters

✍ Sophon Roengsumran; Amorn Petsom; Suthep Thaniyavarn; Surat Prachyakul 📂 Article 📅 1993 🏛 John Wiley and Sons 🌐 English ⚖ 293 KB

Bactericidal and fungicidal activity of

Bactericidal and fungicidal activity of anthranilate esters

✍ Heindel, Ned D.; Lemke, Thomas F.; Lemke, Sally M.; Fish, Velmer B. 📂 Article 📅 1968 🏛 American Chemical Society 🌐 English ⚖ 227 KB

Fungicidal Activities of Dihydroferulic

Fungicidal Activities of Dihydroferulic Acid Alkyl Ester Analogues

✍ Beck, John J.; Kim, Jong H.; Campbell, Bruce C.; Chou, Shen-Chieh 📂 Article 📅 2007 🏛 American Chemical Society 🌐 English ⚖ 47 KB

Polymerization of vinylphosphonic acid e

Polymerization of vinylphosphonic acid esters on complex catalysts

✍ V.F. Sopin; Ye.V. Kuznetsov; Yu.V. Kissin; V.Ye. Nevzorov; N.P. Shestak; V.Ya. I 📂 Article 📅 1977 🏛 Elsevier Science ⚖ 456 KB

Hydrogen-transfer polymerization of viny

Hydrogen-transfer polymerization of vinylphosphonic acid monoethyl ester

✍ Kobayashi, Shiro; Kadokawa, Junichi; Yen, I. Fang; Uyama, Hiroshi; Shoda, Shinic 📂 Article 📅 1992 🏛 American Chemical Society 🌐 English ⚖ 301 KB

Asymmetric hydrogenation of vinylphospho

Asymmetric hydrogenation of vinylphosphonic acids and esters with chiral Ru(II) catalysts

✍ J.-C. Henry; D. Lavergne; V. Ratovelomanana-Vidal; J.-P. Genêt; I.P. Beletskaya; 📂 Article 📅 1998 🏛 Elsevier Science 🌐 French ⚖ 241 KB

The first asymmetric hydrogenation of vinylphosphonic acids and esters to the corresponding arylethylphosphonic acids and esters using chiral Ru(ll) catalysts is reported with enantiomeric excesses up to 86%.