Chirality & Odour Perception
John C. Leffingwell, Ph.D.

The Suzarals

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Photo by permission of M. Roudintska - Art & Parfum

(S)-(+)-Suzaral - ozone-like, clean (Yamamoto)

Ref: T. Yamamato, Advances in the transition metal (Rh, Ru)-BINAP-catalyzed asymmetric chiral compounds for flavours and fragrances and their associated sensory properties, in Current Topics in Flavours and Fragrances - Towards a New Millennium of Discovery, Karl A. D. Swift, Ed., Kluwer Academic Publishers (now Springer), 2000, pp. 33-59, Note that the odor description is based on the (+)-enantiomer as Yamamoto's assignment of the (S) configuration has been reversed.

Suzaral is a trade name of Takasago International

(R)-(-)-Suzaral - lily-of-the-valley, green, floral (Yamamoto)

Ref: T. Yamamato, Advances in the transition metal (Rh, Ru)-BINAP-catalyzed asymmetric chiral compounds for flavours and fragrances and their associated sensory properties, in Current Topics in Flavours and Fragrances - Towards a New Millennium of Discovery, Karl A. D. Swift, Ed., Kluwer Academic Publishers (now Springer), 2000, pp. 33-59, Note that the odor description is based on the (-)-enantiomer as Yamamoto's assignment of the (R) configuration has been reversed.

Suzaral is a trade name of Takasago International

Cyclic Terpenoid Odorants

Bicyclic Terpenoid Odorants

Acyclic Terpenoid Odorants

Ionones, Irones, Damascones & Structurally Related Odorants

Acyclics (Alcohols, Esters, Acids, Aldehydes)

Lactones

Sesquiterpenoid Related Odorants

Steroid Urine Type Odorants

Sandalwood Type Odorants

Musk Odorants

Miscellaneous

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