✦ LIBER ✦

A novel method for the terpene synthesis by the ring-opening reaction of β-methyl-β-propiolactone

✍ Scribed by Tamotsu Fujisawa; Toshio Sato; Tatsuo Kawara; Atsunari Noda; Toshiyuki Obinata

Publisher: Elsevier Science
Year: 1980
Tongue: French
Weight: 177 KB
Volume: 21
Category: Article
ISSN: 0040-4039
DOI: 10.1016/0040-4039(80)80126-2

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

A novel synthesis of (E)-3,7-dimethyl-2-

A novel synthesis of (E)-3,7-dimethyl-2-octene-1,8-diol secreted by the african monarch using the ring-opening reaction of α-methyl-β-propiolactone

✍ Tamotsu Fujisawa; Toshio Sato; Tatsuo Kawara; Atsunari Noda 📂 Article 📅 1982 🏛 Elsevier Science 🌐 French ⚖ 131 KB

The regiosetective ring-opening reaction of a-methyl-B-propiolactone with 3,3-ethytenedioxybutytmagnesiwn bromide in the presence of copper(I) cataZyst afforded 2-methyl-6-oxoheptanoic acid, which was easily converted into IEI-3,7-dimethyl-2-octene-I,&dial in good yield.

ChemInform Abstract: Facile Synthesis of

ChemInform Abstract: Facile Synthesis of β-Hydroxy-δ-valerolactone via the Ring Opening Reaction of β-Trichloromethyl-β-propiolactone with Ester Enolates.

✍ M. SHIMIZU; K. ISHII; T. FUJISAWA 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 32 KB 👁 1 views

A convenient method for the synthesis of

A convenient method for the synthesis of (E)-3-alkenoic acids by a regio- and stereoselective reaction of β-vinyl-β-propiolactone with organocopper reagents

✍ Toshio Sato; Masashi Takeuchi; Toshiyuki Itoh; Masatoshi Kawashima; Tamotsu Fuji 📂 Article 📅 1981 🏛 Elsevier Science 🌐 French ⚖ 245 KB

Reactions of group IV organometallic com

Reactions of group IV organometallic compounds II. Dual behaviour of the ring opening of β-propiolactone by trimethylsilyl-, germyl- and stannyl diethylamine.

✍ Kenji Itoh; Shizuyoshi Sakai; Yoshio Ishii 📂 Article 📅 1966 🏛 Elsevier Science 🌐 French ⚖ 203 KB

Tetraselenotungstate: An Efficient Selen

Tetraselenotungstate: An Efficient Selenating Reagent for the Synthesis of β-Amino Diselenides by Aziridine Ring Opening Reactions.

✍ Devarajulu Sureshkumar; Thanikachalam Gunasundari; Vadivelu Saravanan; Srinivasa 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 24 KB 👁 1 views

A novel method for the synthesis of arom

A novel method for the synthesis of aromatic E-β-chlorovinylketones

✍ Jose Juan Conde; Michael Martucci; Mark Olsen 📂 Article 📅 2000 🏛 Elsevier Science 🌐 French ⚖ 107 KB

The reaction of aromatic acetylenic ketones with aqueous HCl promoted by catalytic FeSO 4 gave a E,Zmixture of b-chlorovinylketones which isomerized almost exclusively to the E-b-isomer upon heating