✦ LIBER ✦

Primary amino acid lithium salt as a catalyst for asymmetric Michael addition of isobutyraldehyde with β-nitroalkenes

✍ Scribed by Sato, Atsushi; Yoshida, Masanori; Hara, Shoji

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: Primary Amino Acid

✍ Atsushi Sato; Masanori Yoshida; Shoji Hara 📂 Article 📅 2009 🏛 John Wiley and Sons ⚖ 26 KB 👁 2 views

Asymmetric Michael addition of aldehydes

✍ Yoshida, Masanori; Sato, Atsushi; Hara, Shoji 📂 Article 📅 2010 🏛 Royal Society of Chemistry 🌐 English ⚖ 254 KB

ChemInform Abstract: Asymmetric Michael

✍ Masanori Yoshida; Atsushi Sato; Shoji Hara 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 60 KB 👁 2 views

Asymmetric Michael Addition of Malonates

✍ Yoshida, Masanori; Narita, Mao; Hara, Shoji 📂 Article 📅 2011 🏛 American Chemical Society 🌐 English ⚖ 888 KB

ChemInform Abstract: Asymmetric Michael

✍ Masanori Yoshida; Mao Narita; Shoji Hara 📂 Article 📅 2012 🏛 John Wiley and Sons ⚖ 47 KB 👁 2 views

## Abstract The title reaction allows an efficient access to a number of optically active 1,5‐ketoesters.