✦ LIBER ✦

An Efficient Diastereoselective Route to Differentially Protected anti -4-Amino-1-alken-3-ols

✍ Scribed by Lombardo, Marco; Mosconi, Elisa; Pasi, Filippo; Petrini, Marino; Trombini, Claudio

Book ID: 120604722
Publisher: American Chemical Society
Year: 2007
Tongue: English
Weight: 75 KB
Volume: 72
Category: Article
ISSN: 0022-3263
DOI: 10.1021/jo062265n

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

An Efficient Diastereoselective Route to

An Efficient Diastereoselective Route to Differentially Protected anti-4-Amino-1-alken-3-ols.

✍ Marco Lombardo; Elisa Mosconi; Filippo Pasi; Marino Petrini; Claudio Trombini 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 37 KB

Isothiazoles. Part IX. An efficient synt

Isothiazoles. Part IX. An efficient synthetic route to 5-substituted-3-amino-4-arylisothiazole 1,1-dioxides and their 4,5-dihydro derivatives

✍ Egle M Beccalli; Francesca Clerici; Maria Luisa Gelmi 📂 Article 📅 1999 🏛 Elsevier Science 🌐 French ⚖ 599 KB

A simple method to introduce an heteroatom substituent at C-5 of isothiazole dioxides is reported. Through Michael addition reaction 5-substituted isothiazole and 4,5-dihydroisothiazole 1,1-dioxides were obtained allowing the preparation of a series of derivatives of special interest for biological

An efficient route to 1,3-amino hydroxyl

An efficient route to 1,3-amino hydroxyl system via electrophilic lactonization of 2-amino-4-pentenoic acid derivatives. Stereoselective synthesis of (−)-bulgecinine

✍ Yasufumi Ohfune; Keiko Hori; Masahiro Sakaitani 📂 Article 📅 1986 🏛 Elsevier Science 🌐 French ⚖ 284 KB

ChemInform Abstract: Isothiazoles. Part

ChemInform Abstract: Isothiazoles. Part 9. An Efficient Synthetic Route to 5-Substituted-3-amino-4-arylisothiazole 1,1-Dioxides and Their 4,5-Dihydro Derivatives.

✍ Egle M. Beccalli; Francesca Clerici; Maria Luisa Gelmi 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 33 KB 👁 2 views

Isothiazoles. Part 9. An Efficient Synthetic Route to 5-Substituted-3-amino-4-arylisothiazole 1,1-Dioxides and Their 4,5-Dihydro Derivatives. -The thiazole dioxide (I) does not react with alcohols, while the derivative (VIII) does not undergo addition with aliphatic and aromatic amines but with the

ChemInform Abstract: Anti-Markovnikov-Fu

ChemInform Abstract: Anti-Markovnikov-Functionalizations of Unsaturated Compounds. Part 3. Base-Catalyzed Hydroamination of Aromatic Olefins — An Efficient Route to 1-Aryl-4-(arylethyl)piperazines.

✍ M. BELLER; C. BREINDL 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 32 KB 👁 1 views

A One-Pot Tandem Ugi Multicomponent Reac

A One-Pot Tandem Ugi Multicomponent Reaction (MCR)/Click Reaction as an Efficient Protecting-Group-Free Route to 1H-1,2,3-Triazole-Modified α-Amino Acid Derivatives and Peptidomimetics

✍ Teng-Fei Niu; Chun Cai; Lan Yi 📂 Article 📅 2012 🏛 John Wiley and Sons 🌐 German ⚖ 264 KB 👁 1 views

## Abstract By a one‐pot tandem __Ugi__ multicomponent reaction (MCR)/click reaction sequence not requiring protecting groups, 1__H__‐1,2,3‐triazole‐modified __Ugi__‐reaction products **6a**–**6n** (__Scheme 1__ and __Table 2__), **7a**–**7b** (__Table 4__), and **8** (__Scheme 2__) were synthesize