๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

The structure of chamaecynone a novel nor-sesquiterpenoid from chamaecyparisformosensis matsum.

โœ Scribed by Tetsuo Nozoe; Y.S. Cheng; Takashi Toda


Publisher
Elsevier Science
Year
1966
Tongue
French
Weight
277 KB
Volume
7
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

โœฆ Synopsis


A reinvestigation of the terpenoid constituents of the Benihi tree (Chamaecyparis formosensis Matsum., Cupressaceae) (l), grown in Formosa, has resulted in the isolationof a novel nor-sesquiterpenoid, chamaecynone (I), which exists in the non-steroid cis-decalin conformation (A) (2.3). This appears to be the first example of a natural acetylenic compound of terpenoid origin (4). Three other closely related nor-sesquiterpanoids, isochamaecynone (II), hydroxyisochsmaecynone (III) and dihydroisochamaecynone (IV) were also isolated besides some other C,, acetylenic compounds. Chamaecynone (I), colorless prisms, m.p. 92'C, (a)D -93.3' (MeOH).


๐Ÿ“œ SIMILAR VOLUMES


The structures of three novel sesquiterp
โœ Dong Sheng Ming; De Quan Yu; Yi Ying Yang; Cun Heng He ๐Ÿ“‚ Article ๐Ÿ“… 1997 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 175 KB

Three new muuiinterpm~ds valefiananoids A(I). B(2) and CO), possessing aa unprecedented seaqmtetpene skeleton, have been isolated from the toots and thizames of V~ jatamansi Jones. The s~ we,re elucidated by chemical and specuoscopic mcam and, in the case of 1, confnmed by X-ray crystallography.

The structure of abscisterol A: A novel
โœ Hiroshi Yada; Hiroji Sato; Shigeru Kaneko; Akitami Ichihara ๐Ÿ“‚ Article ๐Ÿ“… 1994 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 308 KB

Abstmcrt 'llw tstfucm of absciistaol A (l), isolated fmm C.ubii?rinu. has been daennkd as 21~nur-2d-methylene-5a-cholesta-7,17( 20)-E-die~~~,l9~~xy-3~~1 from a ties of 1D and 2D NMR ex&xdIwtslmdaa~~method.

The structure of rupestrol - a new sesqu
โœ V.G.S. Box; W.R. Chan; D.R. Taylor ๐Ÿ“‚ Article ๐Ÿ“… 1971 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 341 KB

We report here the structural elucidation of a new sesquiterpene, rupestrol, which occurs naturally as its orthocinnamate (1) and cinnamate (2) esters in Verbesina rupestris. Rupestrol orthocinnamate (l), C24H3205, m/e 400 (M+), m.p. 206-207", had a trans-styrene unit [Amex 250 nm (E 22,000), vmax 1

Structure and stereochemistry of mexican
โœ Alfonso Romo de Vivar; Guillermo Delgado ๐Ÿ“‚ Article ๐Ÿ“… 1985 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 210 KB

The structure and stereochemistry of mexicanin F, a novel dimeric nor-sesquiterpene lactone isolated from He&n&m mexicanum, have been stablish\_ ed from spectral and single-crystal X-ray analyses. Several years ago, one of us reported the physical constants of the mexicanins A, B,..., H which, in ad