## Abstract A theoretical conformational study based on density functional calculations provides evidence that the sterol and nonsterol cyclizations of squalene to triterpenes are controlled by conformational effects as has been previously suggested. It was found that different conformers of a mode
✦ LIBER ✦
Formation of the B Ring in Steroids and Hopanoids from Squalene
✍ Scribed by B. Andes Hess Jr.
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 67 KB
- Volume
- 2004
- Category
- Article
- ISSN
- 1434-193X
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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v