## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 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
Conformation-Odor Relationships in Norlabdane Oxides
✍ Scribed by Günther Ohloff; Christian Vial; Edouard Demole; Paul Enggist; Wolfgang Giersch; Elise Jégou; Andrew J. Caruso; Judith Polonsky; Edgar Lederer
- Book ID
- 102858163
- Publisher
- John Wiley and Sons
- Year
- 1986
- Tongue
- German
- Weight
- 549 KB
- Volume
- 69
- Category
- Article
- ISSN
- 0018-019X
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✦ Synopsis
Conformational factors have been found responsible for the dramatic change in odor between (-)-deoxyambreinolide (12) and its (+)-epi derivative 13. The presumably molecular event during the receptor interaction has been simulated by the diastereoisomeric 1 1-methyl-ambrox derivatives 3 and 5 as model compounds.
📜 SIMILAR VOLUMES
## Abstract The four possible A/B __cis__‐fused diastereoisomers of __Ambrox__® have been synthesized and their configurations and conformations established by X‐ray and NMR analysis. Only 5β‐ambrox (= 1,2,3a,4,5,5β,6,7,8,9,9a,9bα‐dodecahydro‐3aβ,6,6,9aβ‐tetramethylnaphtho[2,1‐__b__]furan; 5) has a
## Abstract Twelve tricyclic ethers of the labdane and __ent__‐labdane series, **5–16**, have been synthesized; compounds **6–15** are new. The intramolecular C~18~‐acetals **1–4** and the tricyclic ethers **5–16** were submitted to an olfactory test which was characterized by an exceptionally high