𝔖 Bobbio Scriptorium

✦ LIBER ✦

Unusual directive effects in the hydroboration of .beta.,.beta.-disubstituted enamines. Conversion of .alpha.-substituted aldehydes to the corresponding alkenes and .beta.-amino alcohols

✍ Scribed by Singaram, Bakthan; Goralski, Christian T.; Fisher, Gary B.

Book ID: 127140498
Publisher: American Chemical Society
Year: 1991
Tongue: English
Weight: 765 KB
Volume: 56
Category: Article
ISSN: 0022-3263
DOI: 10.1021/jo00019a043

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

.alpha.,.beta.-Epoxy sulfoxides as usefu

.alpha.,.beta.-Epoxy sulfoxides as useful intermediates in organic synthesis. 21. A novel approach to the asymmetric synthesis of epoxides, allylic alcohols, .alpha.-amino ketones, and .alpha.-amino aldehydes from carbonyl compounds through .alpha.,.beta.-epoxy sulfoxides using the optically active p-tolylsulfinyl group to induce chirality

✍ Satoh, Tsuyoshi; Oohara, Teruhiko; Ueda, Yoshiko; Yamakawa, Koji 📂 Article 📅 1989 🏛 American Chemical Society 🌐 English ⚖ 942 KB

Selective reductions. 22. Facile reducti

Selective reductions. 22. Facile reduction of .alpha.,.beta.-unsaturated aldehydes and ketones with 9-borabicyclo[3.3.1]nonane. A remarkably convenient procedure for the selective conversion of conjugated aldehydes and ketones to the corresponding allylic alcohols in the presence of other functional groups

✍ Krishnamurthy, S.; Brown, Herbert C. 📂 Article 📅 1977 🏛 American Chemical Society 🌐 English ⚖ 618 KB