✦ LIBER ✦

A New Method for the Synthesis of β-Amino Acid Derivatives and β-Lactams. Reaction of N-Alkoxycarbonyl-1-methoxyamines with Esters

✍ Scribed by Kise, Naoki; Ueda, Nasuo

Book ID: 115496124
Publisher: American Chemical Society
Year: 1999
Tongue: English
Weight: 60 KB
Volume: 64
Category: Article
ISSN: 0022-3263
DOI: 10.1021/jo990821q

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

ChemInform Abstract: A New Method for th

ChemInform Abstract: A New Method for the Synthesis of β-Amino Acid Derivatives and β-Lactams. Reaction of N-Alkoxycarbonyl-1-methoxyamines with Esters.

✍ Naoki Kise; Nasuo Ueda 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 39 KB 👁 1 views

Asymmetric Synthesis of anti -α,β-Disubs

Asymmetric Synthesis of anti -α,β-Disubstituted β-Amino Acid Derivatives by Reaction of N -Alkoxycarbonyl-1-methoxyamines with Optically Active 2-Oxazolidinones

✍ Kise, Naoki; Ueda, Nasuo 📂 Article 📅 1999 🏛 American Chemical Society 🌐 English ⚖ 153 KB

ChemInform Abstract: Asymmetric Synthesi

ChemInform Abstract: Asymmetric Synthesis of anti-α,β-Disubstituted β-Amino Acid Derivatives by Reaction of N-Alkoxycarbonyl-1-methoxyamines with Optically Active 2-Oxazolidinones.

✍ Naoki Kise; Nasuo Ueda 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 30 KB 👁 1 views

ChemInform Abstract: Intramolecular Este

ChemInform Abstract: Intramolecular Ester Enolate—Imine Cyclization Reactions for the Asymmetric Synthesis of Polycyclic β-Lactams and Cyclic β-Amino Acid Derivatives.

✍ Caroline D. Evans; Mary F. Mahon; Philip C. Andrews; James Muir; Steven D. Bull 📂 Article 📅 2012 🏛 John Wiley and Sons ⚖ 42 KB

ChemInform Abstract: Mannich Type Reacti

ChemInform Abstract: Mannich Type Reactions of Acylhydrazones with Silyl Enolates for the Synthesis of β-Amino Ester, β-Amino Ketone, β-Lactam, Pyrazolidinone, and Pyrazolone Derivatives.

✍ Osamu Okitsu; Hidekazu Oyamada; Takayuki Furuta; Shu Kobayashi 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 36 KB 👁 1 views

Synthesis of (S)- and (R)- tert Leucine

Synthesis of (S)- and (R)- tert Leucine Enabling Direct Coupling with α-Amino Acid Esters via β-Lactam-Derived α-Amino Acid N-Carboxy Anhydrides.

✍ Claudio Palomo*; Iñaki Ganboa; Beatriz Odriozola; Anthony Linden 📂 Article 📅 1997 🏛 Elsevier Science 🌐 French ⚖ 507 KB

3S, 4R)-and (3R, 4S)-3-hydroxy-4-rerr-butyl &lactams on exposure to IM NaOCl and a catalytic amount of 2,2,6,6-tetramethy lpiperidinyl-l-oxyl (TEMPO) afforded et-amino acid N-carboxy anhydrides formally derived from both (S)-and (R)-tert-leucine amino acids. 01997 Published byElsevierScienceLtd.