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Ring Opening/C–N Cyclization of Activated Aziridines with Carbon Nucleophiles: Highly Diastereo- and Enantioselective Synthesis of Tetrahydroquinolines

✍ Scribed by Ghorai, Manas K.; Nanaji, Y.; Yadav, A. K.

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Ring Opening/C—N Cy

✍ Manas K. Ghorai; Y. Nanaji; A. K. Yadav 📂 Article 📅 2011 🏛 John Wiley and Sons ⚖ 55 KB 👁 2 views

Enantioselective Synthesis of 4,5-Dihydr

✍ Ghorai, Manas K.; Tiwari, Deo Prakash 📂 Article 📅 2013 🏛 American Chemical Society 🌐 English ⚖ 884 KB

ChemInform Abstract: Lewis Acid Catalyze

✍ Manas K. Ghorai; Deo Prakash Tiwari 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 51 KB 👁 2 views

## Abstract Starting from alkyl‐substituted aziridines such as (VI) only moderate diastereoselectivity is achieved.

Highly Facialselective Synthesis of Pyra

✍ Yin, Biao-Lin; Zhang, Ze-Ren; Xu, Li-Wen; Jiang, Huanfeng 📂 Article 📅 2011 🏛 American Chemical Society 🌐 English ⚖ 829 KB

ChemInform Abstract: Highly Facialselect

✍ Biao-Lin Yin; Ze-Ren Zhang; Li-Wen Xu; Huanfeng Jiang 📂 Article 📅 2012 🏛 John Wiley and Sons ⚖ 40 KB 👁 1 views

ChemInform Abstract: Asymmetric Catalyti

✍ Joseph M. Ready; Eric N. Jacobsen 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 35 KB 👁 1 views