Chemistry Letters

Organic synthesis using haloboration reaction. 15. The Michael-type reaction of B-iodo-9-BBN/ethoxyethyne adduct to. ALPHA.,. BETA.-unsaturated ketones. A …

F Kawamura, T Tayano, Y Satoh, S Hara, A Suzuki

Index: Kawamura, Fumitoshi; Tayano, Takao; Satoh, Yoshitaka; Hara, Shoji; Suzuki, Akira Chemistry Letters, 1989 , p. 1723 - 1726

Full Text: HTML

Citation Number: 10

Abstract

CHEMISTRY LETTERS, pp. 172371726, 1989. © 1989 The Chemical Society of Japan The Michael—type Reaction of B—Iodo—9—BBN/Ethoxyethyne Adduct to d,8—Unsaturated Ketones. A Selective Synthesis of G—Keto Esters1) Fumitoshi KAWAMURA, Takao TAYANO, Yoshitaka SATOH, Shoji HARA, and Akira SUZUKI* Department of Applied Chemistry, Faculty of Engineering, Hokkaido University, Sapporo 060 The adduct formed ...

Related Articles:

Michael addition of stannyl ketone enolate to α, β-unsaturated esters catalyzed by tetrabutylammonium bromide and an ab initio theoretical study of the …

[Yasuda, Makoto; Chiba, Kouji; Ohigashi, Noriyuki; Katoh, Yasuhiro; Baba, Akio Journal of the American Chemical Society, 2003 , vol. 125, # 24 p. 7291 - 7300]

Reactions of Grignard Reagents with Bis-or Mono-Phosphonium lons in Situ Generated from Bu3P and Dicarboxylic Acid Dichlorides or. OMEGA.-Ethoxycarbonyl …

[Maeda; Hino; Yamauchi; Ohmori Chemical and Pharmaceutical Bulletin, 2000 , vol. 48, # 8 p. 1196 - 1199]

Nucleophilic Substitution Reactions at Chloro-Substituted Ozonides and at a Chlorinated Dimeric Peroxide

[Journal of Organic Chemistry, , vol. 60, # 24 p. 8062 - 8066]

Synthesen mit Acetessigsäure??tert.??butylester

[Chemische Berichte, , vol. 87, p. 1163,1166]

The base catalysed reaction of acetylacetone and acrylate esters

[Australian Journal of Chemistry, , vol. 20, p. 123 - 130]

More Articles...