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ChemInform Abstract: Reductive 1,2-Allylboration of Indoles by Triallyl- and Triprenylborane — Synthesis of 2-Allylated Indolines.

✍ Scribed by Yury N. Bubnov; Ilya V. Zhun'; Elena V. Klimkina; Anatoly V. Ignatenko; Zoya A. Starikova

Publisher
John Wiley and Sons
Year
2001
Weight
29 KB
Volume
32
Category
Article
ISSN
0931-7597

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📜 SIMILAR VOLUMES

Reductive 1,2-Allylboration of Indoles b
Reductive 1,2-Allylboration of Indoles by Triallyl- and Triprenylborane − Synthesis of 2-Allylated Indolines
✍ Yury N. Bubnov; Ilya V. Zhun'; Elena V. Klimkina; Anatoly V. Ignatenko; Zoya A. 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 265 KB 👁 1 views

Indoles undergo reductive α-allylation upon treatment with allylic boranes (triallyl-and triprenylborane) to give, after deboronation, the corresponding 2-allylated indolines in 70-85% yield. 1,2-Addition of the allylboron fragment to heterocycles occurs with full rearrangement of the allylic moiety

ChemInform Abstract: Synthesis of N-Ally
ChemInform Abstract: Synthesis of N-Allylanilines by the Reductive Allylboration of Aromatic Nitro Compounds.
✍ Yurii N. Bubnov; Dmitrii G. Pershin; Anatolii V. Ignatenko; Mikhail E. Gurskii 📂 Article 📅 2000 🏛 John Wiley and Sons ⚖ 27 KB 👁 1 views

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