✦ LIBER ✦

Ring-Closing Metathesis of Chiral Allylamines. Enantioselective Synthesis of (2S,3R,4S)-3,4-Dihydroxyproline.

✍ Scribed by Ruben Martin; Montserrat Alcon; Miquel A. Pericas; Antoni Riera

Publisher: John Wiley and Sons
Year: 2003
Weight: 261 KB
Volume: 34
Category: Article
ISSN: 0931-7597
DOI: 10.1002/chin.200311056

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Synthesis of trans-(3S)-Amino-(4R)-alkyl

Synthesis of trans-(3S)-Amino-(4R)-alkyl- and -(4S)-aryl-piperidines via Ring-Closing Metathesis Reaction.

✍ X. Eric Hu; Nick K. Kim; Benoit Ledoussal 📂 Article 📅 2003 🏛 John Wiley and Sons ⚖ 139 KB 👁 1 views

Synthesis of (2R,3S,4S)-4-Aryl-3-hydroxy

Synthesis of (2R,3S,4S)-4-Aryl-3-hydroxyprolinols.

✍ Meng-Yang Chang; Chun-Yu Lin; Tsun-Cheng Wu 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 27 KB 👁 1 views

ChemInform Abstract: Synthesis of (2S,3R

ChemInform Abstract: Synthesis of (2S,3R,4S), (2S,3S,4R)-Epoxyprolines and Aminohydroxyprolines.

✍ J. K. ROBINSON; V. LEE; T. D. W. CLARIDGE; J. E. BALDWIN; C. J. SCHOFIELD 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 40 KB 👁 1 views

Facile Synthesis of Azocino[4,3-b]indole

Facile Synthesis of Azocino[4,3-b]indoles by Ring-Closing Metathesis.

✍ M.-Lluisa Bennasar; Ester Zulaica; Daniel Sole; Sandra Alonso 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 38 KB

ChemInform Abstract: Stereodivergent Syn

ChemInform Abstract: Stereodivergent Synthesis of (2S,3S,4R,5R)- and (2S,3S,4R,5S)-[3,4,5-D3]Proline Depending on the Substituent of the γ-Lactam Ring.

✍ Makoto Oba; Akiko Miyakawa; Kozaburo Nishiyama; Tsutomu Terauchi; Masatsune Kain 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 42 KB 👁 1 views

Synthesis and α-Mannosidase Inhibitory E

Synthesis and α-Mannosidase Inhibitory Evaluation of (2R,3R,4S)- and (2S,3R,4S)-2-(Aminomethyl)pyrrolidine-3,4-diol Derivatives

✍ Florence Popowycz; Sandrine Gerber-Lemaire; Eliazar Rodriguez-García; Catherine 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 German ⚖ 485 KB 👁 1 views

The synthesis of 46 derivatives of (2R,3R,4S)-2-(aminomethyl)pyrrolidine-3,4-diol is reported (Scheme 1 and Fig. 3), and their inhibitory activities toward a-mannosidases from jack bean (B) and almonds (A) are evaluated (Table ). The most-potent inhibitors are (2R,3R,4S)-2-{[([1,1'-biphenyl]-4-ylmet