✦ LIBER ✦

THE MOVEMENT TOWARDS SYNTHETIC STUDIES, AND ITS EDUCATIONAL AND SOCIAL BEARINGS

✍ Scribed by P. Gkddes

Book ID: 117951532
Publisher: John Wiley and Sons
Year: 1928
Tongue: English
Weight: 622 KB
Volume: a20
Category: Article
ISSN: 0038-0261
DOI: 10.1111/j.1467-954x.1928.tb01661.x

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

THE HOMECROFT MOVEMENT: ITS SOCIAL AND E

THE HOMECROFT MOVEMENT: ITS SOCIAL AND EDUCATIONAL ASPECTS

✍ J. W. Scott 📂 Article 📅 1928 🏛 John Wiley and Sons 🌐 English ⚖ 222 KB

EXPERIMENTAL EDUCATION: ITS BEARING ON S

EXPERIMENTAL EDUCATION: ITS BEARING ON SOCIAL AND BEHAVIORAL RESEARCH

✍ HENRY WINTHROP 📂 Article 📅 1965 🏛 John Wiley and Sons 🌐 English ⚖ 512 KB

Synthetic studies towards (±)-aristeromy

Synthetic studies towards (±)-aristeromycin and its 5′-homo-analogue

✍ H. Kapeller; H. Baumgartner; H. Griengl 📂 Article 📅 1997 🏛 Springer Vienna 🌐 English ⚖ 637 KB

ChemInform Abstract: Synthetic Studies T

ChemInform Abstract: Synthetic Studies Towards (.+-.)-Aristeromycin and Its 5′-homo- Analogue.

✍ H. KAPELLER; H. BAUMGARTNER; H. GRIENGL 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 31 KB 👁 2 views

Synthetic Studies Towards (±)-Aristeromycin and Its 5'-homo-Analogue. -A new synthetic pathway to the two title compounds (VIIb) and (VIII) involving nucleophilic substitution of a sulfonate ester group (IV) by the aglycone is reported.

THE NATURE AND SOCIAL BASES OF PROGRESSI

THE NATURE AND SOCIAL BASES OF PROGRESSIVE SOCIAL MOVEMENT IDEOLOGY: Examining Public Opinion toward Social Movements

✍ Aaron M. McCright; Riley E. Dunlap 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 164 KB

Synthetic studies towards the squalestat

Synthetic studies towards the squalestatins and zaragozic acids

✍ Leasa M. McVinish; Mark A. Rizzacasa 📂 Article 📅 1994 🏛 Elsevier Science 🌐 French ⚖ 293 KB

A synthesis of a mod core sysmn (18) of the sqdestatins and saragozic acids has been achieved y?om D-mannose. The key steps intive an Irehd-Chisen reawan~emeni of the ally1 ester 5 ad a stereoselective epoxidktion of the f&add glycd 12 with 2&dimethyl&xkne. A number of structurally related compounds