✦ LIBER ✦

Stereoselective total synthesis of penaresidin A starting from d-galactal

✍ Scribed by Reddy, B.V. Subba; Kishore, Ch.; Reddy, A. Srinivas

Book ID: 123124629
Publisher: Elsevier Science
Year: 2014
Tongue: French
Weight: 600 KB
Volume: 55
Category: Article
ISSN: 0040-4039
DOI: 10.1016/j.tetlet.2013.10.095

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

A convenient stereoselective synthesis o

A convenient stereoselective synthesis of D-erythro-C18-sphingosine from galactal

✍ Hirata, Norihiko; Yamagiwa, Yoshiro; Kamikawa, Tadao 📂 Article 📅 1991 🏛 Royal Society of Chemistry ⚖ 199 KB

ChemInform Abstract: Chiral and Stereose

ChemInform Abstract: Chiral and Stereoselective Total Synthesis of (-)-Mesembranol Starting from D-Glucose.

✍ N. CHIDA; K. SUGIHARA; S. AMANO; S. OGAWA 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 35 KB 👁 2 views

Stereoselective total synthesis of (+)-l

Stereoselective total synthesis of (+)-lactacystin from d-glucose

✍ Noritaka Chida; Jun Takeoka; Kohji Ando; Noriko Tsutsumi; Seiichiro Ogawa 📂 Article 📅 1997 🏛 Elsevier Science 🌐 French ⚖ 776 KB

The chiral and stereoselective synthesis of (+)-lactacystin 1, the first non-protein neurotrophic factor having an ct,~t-disubstituted a-amino acid structure, is described. The highly functionalized y-lactam portion possessing a tetra-substituted carbon with nitrogen in I was effectively constructed

Stereoselective total synthesis of (+)-m

Stereoselective total synthesis of (+)-myriocin from d-mannose

✍ Oishi, Takeshi; Ando, Koji; Chida, Noritaka 📂 Article 📅 2001 🏛 Royal Society of Chemistry 🌐 English ⚖ 80 KB

Stereoselective Total Synthesis of (-)-S

Stereoselective Total Synthesis of (-)-Synrotolide Diacetate from D-Ribose.

✍ Palakodety Radha Krishna; P. Srinivas Reddy 📂 Article 📅 2007 🏛 John Wiley and Sons ⚖ 12 KB 👁 2 views

Synthesis of a tetrahydrofuran fragment

Synthesis of a tetrahydrofuran fragment of annonaceous acetogenin from d-galactal

✍ Lénaïck Lemée; Anne Jégou; Alain Veyrières 📂 Article 📅 1999 🏛 Elsevier Science 🌐 French ⚖ 252 KB

Iodoeyclisation of 6-O-pivaloyl-D-galaetal followed by radical reduction at C-2 and SN 2 conversion to a 3-endo iodide gave in good yield a [2.2.1] bicyclic acetal which can be regioselectively opened by C-nucleophiles (aUyl silane or silyloxyfuran) in the presence of a Lewis acid to give 2,5-trans-