𝔖 Bobbio Scriptorium
✦   LIBER   ✦

2-Bromoallyl Acetate: A Useful Structural Unit for Sequential Carbon−Carbon Bond Formation

✍ Scribed by Taylor, Richard E.; Ciavarri, Jeffrey P.

Book ID
121422968
Publisher
American Chemical Society
Year
1999
Tongue
English
Weight
48 KB
Volume
1
Category
Article
ISSN
1523-7060

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Sequential carbon-carbon bond formation
Sequential carbon-carbon bond formation reaction using 1-silyl-2-propenyllithium
✍ Koji Takaku; Hiroshi Shinokubo; Koichiro Oshima 📂 Article 📅 1998 🏛 Elsevier Science 🌐 French ⚖ 202 KB

The reaction of l-triphenylsilyl-2-propenyllithium with ethylene oxide afforded an adduct, a lithium salt of 3-triphenylsilyl-4-penten-I-ol, which regenerated an allyllithium species, 3-1ithio-5triphenylsiloxy-l-pentene via anionic rearrangement ofa silyl group from carbon to oxide in the presence o

ChemInform Abstract: Sequential Carbon—C
ChemInform Abstract: Sequential Carbon—Carbon Bond Formation Reaction Using 1-Silyl-2-propenyllithium.
✍ K. TAKAKU; H. SHINOKUBO; K. OSHIMA 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 36 KB 👁 1 views

## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v

A carbon-carbon bond formation using end
A carbon-carbon bond formation using endoperoxides of 1,2-dihydropyridines
✍ Mitsutaka Natsume; Yasuo Sekine; Masashi Ogawa; Hiroe Soyagimi; Yoshinori Kitaga 📂 Article 📅 1979 🏛 Elsevier Science 🌐 French ⚖ 246 KB

A novel type of a nucleophilic substitution on the piperidine ring was achieved by a stannous chloride-effected reaction of endoperoxides of N-