✦ LIBER ✦

Pausanias 3.14.1: A Sidelight on Spartan History, C. 440 B.C.?

✍ Scribed by W. R. Connor

Book ID: 123739309
Publisher: John Hopkins University Press
Year: 1979
Tongue: English
Weight: 661 KB
Volume: 109
Category: Article
ISSN: 1533-0699
DOI: 10.2307/284046

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Toxicity of fumonisin B1 to B6C3F1 mice:

Toxicity of fumonisin B1 to B6C3F1 mice: A 14-day gavage study

✍ G.S Bondy; C.A.M Suzuki; S.M Fernie; C.L Armstrong; S.L Hierlihy; M.E Savard; M. 📂 Article 📅 1997 🏛 Elsevier Science 🌐 English ⚖ 805 KB

1,4-Cycloaddition reactions. V. Preparat

1,4-Cycloaddition reactions. V. Preparation of 1,2,14b, 14c-tetrahydro-3a-methyl-3aH-furo[3′,2′:3,4] quino-[1,2-c] [1,2,3] benzotriazine via povarov precursors

✍ Donald F. Worth; Edward F. Elslager; S. C. Perricone 📂 Article 📅 1974 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 122 KB

The synthesis of (−)-4-methyl-8-chloro-t

The synthesis of (−)-4-methyl-8-chloro-trans-1,2,3,4,4a,5,6,10b-octahydrobenzo-[f]-quinolin-3-one-[3-14C] (LY300502-14C]) via a circuitous route

✍ Fengjiun Kuo; William J. Wheeler 📂 Article 📅 1994 🏛 John Wiley and Sons 🌐 French ⚖ 340 KB 👁 1 views

## Abstract The synthesis of the C‐14 labeled isotopomer of LY300502, a potent 5α‐reductase inhibitor has been accomplished in four radiochemical steps. The route involves the synthesis of LY300502‐[^14^C] from LY300502 __via__ a circuitous route; the label was introduced with ethyl chloroformate‐[

A Novel Synthesis of Pyrano(2,3-c)-, 1,3

A Novel Synthesis of Pyrano(2,3-c)-, 1,3-Oxazino(2,3 b)-,1,2,4-Triazolo(3,4-b)-, Oxazolo(2,3-b)-, Furano(3,2-c)-, and 3-Substituted-(1,5)benzodiazepin-2-ones

✍ El-snyed, A. M.; Abdel-ghany, H.; El-snghier, A. M. M. 📂 Article 📅 1999 🏛 Taylor and Francis Group 🌐 English ⚖ 375 KB

14b-Chloro-4a-methoxy-3,3-dimethyl-2,3,4

14b-Chloro-4a-methoxy-3,3-dimethyl-2,3,4a,14b-tetrahydro-1H-benzo[a]pyrano[2,3-c]phenazine: a new active structural type against Mycobacterium tuberculosis

✍ Nunes, I. K. da C. ;De Simone, C. A. ;Silva, R. S. F. ;Pinto, A. V. ;Goulart, M. 📂 Article 📅 2007 🏛 International Union of Crystallography 🌐 English ⚖ 763 KB

The title compound, C 22 H 21 ClN 2 O 2 , obtained from the reaction of the phenazine of -lapachone with trichloroisocyanuric acid, showed a minimum inhibitory concentration of 6.25 ng ml À1 in tuberculostatic assays against Mycobacterium tuberculosis and established a new structural type with poten

ChemInform Abstract: A Novel Synthesis o

ChemInform Abstract: A Novel Synthesis of Pyrano[2,3-c]-, 1,3-Oxazino[2,3-b]-, 1,2,4-Triazolo[3,4-b]-, Oxazolo[2,3-b]-, Furano[3,2-c]-, and 3-Substituted-[1,5]benzodiazepin-2-ones.

✍ A. M. El-Sayed; H. Abdel-Ghany; A. M. M. El-Saghier 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 34 KB 👁 1 views