✦ LIBER ✦

Derivatives of Morpholine. I. Addition to Conjugate Systems. I.

✍ Scribed by Stewart, Vincent E.; Pollard, C. B.

Book ID: 111906268
Publisher: American Chemical Society
Year: 1937
Tongue: English
Weight: 100 KB
Volume: 59
Category: Article
ISSN: 0002-7863
DOI: 10.1021/ja01291a066

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Addition of Heterocycles to Conjugate Un

Addition of Heterocycles to Conjugate Unsaturated Carbonyl Compounds: Difunctional Derivatives

✍ Webb, I. D.; Borcherdt, G. T. 📂 Article 📅 1951 🏛 American Chemical Society 🌐 English ⚖ 276 KB

Cu(I)-Catalyzed Conjugate Addition of Et

Cu(I)-Catalyzed Conjugate Addition of Ethyl Propiolate.

✍ Shinji Fujimori; Erick M. Carreira 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 44 KB

Conjugate Addition of Organomagnesium Cu

Conjugate Addition of Organomagnesium Cuprates to Guvacine Derivatives

✍ Hellenbrand, Tim; Wanner, Klaus T. 📂 Article 📅 2014 🏛 John Wiley and Sons 🌐 English ⚖ 334 KB

Rh(I)-catalyzed addition of alkenylzirco

Rh(I)-catalyzed addition of alkenylzirconocene chlorides to aldimine derivatives

✍ Akito Kakuuchi; Takeo Taguchi; Yuji Hanzawa 📂 Article 📅 2003 🏛 Elsevier Science 🌐 French ⚖ 139 KB

RhCl(COD)] 2 (2 mol%) catalyzed reactions of alkenylzirconocene chloride complexes to N-Ts, -PO(OEt) 2 and COOR aldimine derivatives were efficiently carried out in dioxane at room temperature to give allylic amine derivatives in excellent yields. This is the first example of the catalytic addition

Rh(I)-Catalyzed Addition of Alkenylzirco

Rh(I)-Catalyzed Addition of Alkenylzirconocene Chlorides to Aldimine Derivatives.

✍ Akito Kakuuchi; Takeo Taguchi; Yuji Hanzawa 📂 Article 📅 2003 🏛 John Wiley and Sons ⚖ 176 KB 👁 2 views

Synthesis of α-amino acid derivatives by

Synthesis of α-amino acid derivatives by copper(I)-catalyzed conjugate addition of grignard reagents to methyl 2-acetamidoacrylate

✍ C. Cardellicchio; V. Fiandanese; G. Marchese; F. Naso; L. Ronzini 📂 Article 📅 1985 🏛 Elsevier Science 🌐 French ⚖ 221 KB

The reactions of Grignard reagents with methyl 2-acetamidoacrylate in the presente of CuI give fair to good yields of cr-amino esters; the corresponding a-deutero-or a-methyl-derivatives are obtained upon quenching with D+ or CH31, respectively.