๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

1961

โœ Scribed by Peonia Rossa


Book ID
108815587
Tongue
Italian
Weight
2 MB
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,