𝔖 Bobbio Scriptorium
✦   LIBER   ✦

A One-Step Synthesis of 1-Halo-ω,ω-Diphenylalkanes

✍ Scribed by Bunce, Richard A. ;Sullivan, James P.

Book ID
115517741
Publisher
Taylor and Francis Group
Year
1990
Tongue
English
Weight
225 KB
Volume
20
Category
Article
ISSN
0039-7911

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

A one step synthesis of ω-hydroxyacetyle
A one step synthesis of ω-hydroxyacetylenic carboxylic acids
✍ J. Cossy; J.P. Pete 📂 Article 📅 1986 🏛 Elsevier Science 🌐 French ⚖ 125 KB

A convenientchemioselectivemethod to prepare w-hydroxyacetylenic carboxylic acids from unprotected w-alkyn-1 01s and w-bromo acids is described.

Cyclization reactions of ω-tosyloxy-1-al
Cyclization reactions of ω-tosyloxy-1-alkynyl- and ω-tosyloxy-1-alkenylborates and their ω-halo analogues
✍ Ei-ichi Negishi; Thinh Nguyen; Larry D. Boardman; Hiroyuki Sawada; James A. Morr 📂 Article 📅 1992 🏛 John Wiley and Sons 🌐 English ⚖ 824 KB

The reaction of trialkylboranes with wtosyloxy-l-lithio-1-alkynes can induce transfer of a n alkyl group froiii the boron atom to the alkynyl carbon atom with concomitant formation of four-through six-menibered carbocycles via intramolecular displacement of the w tosyloxy group. The stereoselectivit

A general synthesis of long chain ω- and
A general synthesis of long chain ω- and (ω-1)-hydroxy fatty acids
✍ Suzanne R. Abrams 📂 Article 📅 1981 🏛 Elsevier Science 🌐 English ⚖ 294 KB

A method for the synthesis of long chain fatty acids substituted at the to and to-1 positions has been developed. The key step is the isomerization of the triple bond of an alkyn-l-ol from an internal position in the chain to the free terminus with a new, convenient reagent, sodium aminopropylamide