✦ LIBER ✦

Communications - Hydroboration of Olefins. A Remakably Fast Room-Temperature Addition of Diborane to Olefins

✍ Scribed by Brown, Herbert; Rao, B. C.

Book ID: 120047054
Publisher: American Chemical Society
Year: 1957
Tongue: English
Weight: 262 KB
Volume: 22
Category: Article
ISSN: 0022-3263
DOI: 10.1021/jo01360a625

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Hydroboration. II. A Remarkably Fast Add

Hydroboration. II. A Remarkably Fast Addition of Diborane to Olefins—Scope and Stoichiometry of the Reaction

✍ Brown, Herbert C.; Rao, B. C. Subba 📂 Article 📅 1959 🏛 American Chemical Society 🌐 English ⚖ 959 KB

Triethylborane-Initiated Room Temperatur

Triethylborane-Initiated Room Temperature Radical Addition of Hypophosphites to Olefins: Synthesis of Monosubstituted Phosphinic Acids and Esters

✍ Deprèle, Sylvine; Montchamp, Jean-Luc 📂 Article 📅 2001 🏛 American Chemical Society 🌐 English ⚖ 129 KB

ChemInform Abstract: Triethylborane-Init

ChemInform Abstract: Triethylborane-Initiated Room Temperature Radical Addition of Hypophosphites to Olefins: Synthesis of Monosubstituted Phosphinic Acids and Esters.

✍ Sylvine Deprele; Jean-Luc Montchamp 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 34 KB 👁 2 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

Hydroboration. 66. Addition of lithium t

Hydroboration. 66. Addition of lithium triethylborohydride to substituted styrenes. A simple, convenient procedure for the Markovnikov hydroboration of aromatically conjugated olefins and the synthesis of unusual mixed trialkylboranes

✍ Brown, Herbert C.; Kim, Suk Choong 📂 Article 📅 1984 🏛 American Chemical Society 🌐 English ⚖ 910 KB

Additions and Corrections - Hydroboratio

Additions and Corrections - Hydroboration. XXXVI. A Direct Route to 9-Borabicyclo-[3.3.1]nonane via the Cyclic Hydrobarotion of 1,5-Cyclooctadiene. 9-Borabicyclo[3.3.1]nonane as a Uniquely Selective Reagent for the Hydroboration of Olefins.

✍ Brown, Herbert; Knights, Evord; Scouten, Charles 📂 Article 📅 1975 🏛 American Chemical Society 🌐 English ⚖ 107 KB