✦ LIBER ✦

Sibyllimycin, 5, 6, 7, 8-Tetrahydro-3-methyl-8-oxo-4-azaindolizidin, ein neuartiger Metabolit aus Thermoactinomyces sp.

✍ Scribed by Doris Hafenbradl; Dr. Martin Keller; Prof. Karl O. Stetter; Priv.-Doz. Dr. Peter Hammann; Frank Hoyer; Dr. Herbert Kogler

Book ID: 101531389
Publisher: John Wiley and Sons
Year: 1996
Tongue: English
Weight: 365 KB
Volume: 108
Category: Article
ISSN: 0044-8249
DOI: 10.1002/ange.19961080519

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Sibyllimycine, 5,6,7,8-Tetrahydro-3-meth

Sibyllimycine, 5,6,7,8-Tetrahydro-3-methyl-8-oxo-4-azaindolizidine, a Novel Metabolite from Thermoactinomyces sp.

✍ Dipl.-Biol. Doris Hafenbradl; Dr. Martin Keller; Prof. Dr. Karl O. Stetter; Priv 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 381 KB

Isolation and Synthesis of N-(2-Methyl-3

Isolation and Synthesis of N-(2-Methyl-3-oxodec-8-enoyl)-2-pyrroline and 2-(Hept-5-enyl)-3-methyl-4-oxo-6,7,8,8a-tetrahydro-4H-pyrrolo[2,1-b]1,3-oxazine – Two New Fungal Metabolites with in vivo Anti-Juvenile-Hormone and Insecticidal Activity

✍ Ángel Cantín; Pilar Moya; Maria-Angeles Castillo; Jaime Primo; Miguel A. Miranda 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 132 KB 👁 2 views

Two new natural products, N- (2-methyl-3-oxodec-8-enoyl)corresponding acid chloride, in order to acylate Meldrum's acid. Subsequent aminolysis with pyrrolidine, followed by 2-pyrroline (2) and 2-(hept-5-enyl)-3-methyl-4-oxo-6,7,8,8atetrahydro-4H-pyrrolo[2,1-b]-1,3-oxazine (3), have been methylation

ChemInform Abstract: Synthesis of N-{[4-

ChemInform Abstract: Synthesis of N-{[4-(2-Amino-4(3H)-oxo-5,6,7,8-tetrahydro-(9H)-pyrimido [4,5-b]azepin-6-yl)methyl]benzoyl}-L-glutamic Acid and Two of Its Conformationally-Restricted Analogues.

✍ Mark W. Read; Michael L. Miller; Partha S. Ray 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 47 KB 👁 1 views

Synthesis of [14C]KT3-671, 2-Propyl-8-ox

Synthesis of [14C]KT3-671, 2-Propyl-8-oxo-1-[ (2′-(1H-[14C] tetrazole-5-yl) biphenyl-4-yl) methyl]-4,5,6, 7-tetrahydro-cycloheptimidazole, a novel potent nonpeptide angiotensin II receptor antagonist

✍ Naoto Ueyama; Takashi Yanagisawa; Tsuyoshi Tomiyama 📂 Article 📅 1995 🏛 John Wiley and Sons 🌐 French ⚖ 263 KB 👁 1 views

## Abstract 2‐Propyl‐8‐oxo‐1‐[(2′‐(1H‐tetrazole‐5‐yl) biphenyl‐4‐yl)methyl]‐4, 5, 6, 7‐tetrahydrocyclohept imidazole (KT3‐671), which has been found to be a potent and selective angiotesin II receptor antagonist, was synthesized in ^14^C‐labelled form by using potassium[^14^C]‐cyanide. [^14^C](KT3‐