๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

1961

โœ Scribed by Peonia Rossa


Book ID
108815739
Tongue
Italian
Weight
253 KB
Category
Fiction

No coin nor oath required. For personal study only.


๐Ÿ“œ SIMILAR VOLUMES


The structure of the macrolide antibioti
โœ Carl Djerassi; M. Ishikawa; H. Budzikiewicz; J.N. Shoolery; L.F. Johnson ๐Ÿ“‚ Article ๐Ÿ“… 1961 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 366 KB
The direct oxidative conversion of 2-met
โœ E.E. van Tamelen; V.B. Haarstad ๐Ÿ“‚ Article ๐Ÿ“… 1961 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 135 KB

THE structural stinilarity between cinchonamine (I) and cinchonine (II) leads to the indisputable conclusion that these two alkaloids are biochemically related, 1 and hypothetical schemes which assume production of the guinoline from the indole base have been roughly outlined by previous authors. 1,

The structure of loganin
โœ Kirti Sheth; Egil Ramstad; Joseph Wolinsky ๐Ÿ“‚ Article ๐Ÿ“… 1961 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 176 KB

IN this communication we wish to report that loganin (C17H26010), a glycoside isolated from Strvchnos nux-vomica 1,2,3 and other Strvchnos species,4J5 has the constitution represented by formula (I). I The glucosidic nature and the presence of one additional free hydroxyl group in loganin, m.p. 222+

A method for exploring the dipolar chara
โœ N.S. Crossley; A.C. Darby; H.B. Henbest; J.J. McCullough; B. Nicholls; M.F. Stew ๐Ÿ“‚ Article ๐Ÿ“… 1961 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 278 KB

THE study of the direction of addition of reagents to unsymmetrically substituted open chain olefins has a long history, but until recently,' very rXh less information has been available concerning the effects of substituents on the direction of addition of reagents to cyclic olefinic bonds in a pla

Optical stability of a nine-membered rin
โœ Kurt Mislow; Seymour Hyden; Hans Schaefer ๐Ÿ“‚ Article ๐Ÿ“… 1961 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 195 KB

THE stereochemistry of 1,2,3,4-dibenzcy~ionona-I,3-diene-~-carboxylic acid (I) is of considerable interest for several reasons. A nine-membered ring bridged biphenyl No.12 conveniently prepared from IIa by LiAlH4 reduction of the ethyl ester to IId,