𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Biosynthesis of stigmasta-7, E-24(28)-dien-3β-ol and 24α-alkyl sterols in Bryonia dioica

✍ Scribed by L. Cattel; G. Balliano; O. Caputo; L. Delprino


Publisher
Elsevier Science
Year
1980
Tongue
English
Weight
228 KB
Volume
19
Category
Article
ISSN
0031-9422

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


5α-24-Norcholestan-3β-ol and (24Z)-Stigm
✍ Claude Delseth; Luhata Tolela; Carl Djerassi; Paul J. Scheuer; Robert J. Wells 📂 Article 📅 1979 🏛 John Wiley and Sons 🌐 German ⚖ 607 KB

## Abstract The steroidal components of 2 marine sponges, __Terpios zeteki__ (from Hawaii) and __Dysidea herbacea__ (from Australia) were fractionated through a combination of chromatographic methods, including reversed phase HPLC., and were analyzed by a combination of physical methods, including

Minor and Trace Sterols in Marine Invert
✍ W. C. M. C. Kokke; C. S. Pak; William Fenical; Carl Djerassi 📂 Article 📅 1979 🏛 John Wiley and Sons 🌐 German ⚖ 563 KB

## Abstract In addition to the two new sterols verongulasterol **11** and 25‐dehydroaplysterol **13** of __Verongia cauliformis__^3^), which were reported earlier [2] [3], the minor and trace sterols of this sponge include five new sterols listed in the title (with the exception of the known 24 __S

High-performance thin-layer chromatograp
✍ Richa Pandey; Ram K. Verma; Madan M. Gupta 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 482 KB

## Abstract A sensitive, selective, precise, and robust high‐performance thin‐layer chromatography method was developed and validated for analysis of two new recently isolated sterols, 4α‐methyl‐24β‐ethyl‐5α‐cholesta‐14,25‐dien‐3β‐ol (**1**) and 24β‐ethylcholesta‐5,9(11),22__E__‐trien‐3β‐ol (**2**)

ChemInform Abstract: An Alternative Synt
✍ B. RUAN; W. K. WILSON; G. J. JUN. SCHROEPFER 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 38 KB 👁 1 views

An Alternative Synthesis of 4,4-Dimethyl-5α-cholesta-8,14,24-trien-3β-ol, an Intermediate in Sterol Biosynthesis and a Reported Activator of Meiosis and of Nuclear Orphan Receptor LXRα. -The title compound (V) is synthesized by a simple six-step procedure. A key step in this synthesis is the highly