1
Richard M Boden, Steven D Temes, Theodore J Tyszkiewicz, Marie R Hanna: Branched C.sub.13 -alk-1-en-5-ones and use thereof in perfumery. International Flavors & Fragrances, Arthur L Liberman, August 13, 1985: US04534891 (59 worldwide citation)

Described are compounds defined according to the structure: ##STR1## wherein R.sub.3, R.sub.4, R.sub.5, R.sub.6 and R.sub.7 represent hydrogen or methyl with the provisos that:


2
Richard M Boden, Manfred H Vock, Theodore J Tyszkiewicz: Prenyl methyl carbonate and organoleptic uses thereof. International Flavors & Fragrances, Arthur L Liberman, December 13, 1983: US04420472 (12 worldwide citation)

Processes and compositions are described for use in foodstuff, chewing gum, toothpaste and medicinal product flavor and aroma augmenting, modifying, enhancing and imparting compositions and as foodstuffs, chewing gums, toothpastes and medicinal product aroma imparting materials of prenyl methyl carb ...


3
Richard M Boden, Manfred H Vock, Theodore J Tyszkiewicz: Prenyl methyl carbonate and organoleptic uses thereof. International Flavors & Fragrances, Arthur L Liberman, May 1, 1984: US04446157 (12 worldwide citation)

Processes and compositions are described for use in foodstuff, chewing gum, toothpaste and medicinal product flavor and aroma augmenting, modifying, enhancing and imparting compositions and as foodstuffs, chewing gums, toothpastes and medicinal product aroma imparting materials of prenyl methyl carb ...


4
Richard M Boden, Theodore J Tyszkiewicz, Michael Licciardello, Manfred H Vock, Joaquin F Vinals, Patrick Whalen, Marie R Hanna: Process for preparing a methoxybenzaldehyde from the corresponding phenolic benzaldehyde. International Flavors & Fragrances, Arthur L Liberman, May 7, 1985: US04515987 (11 worldwide citation)

Described is a genus of compounds defined according to the structure: ##STR1## (Z) represents one of the moieties ##STR2## as well as the substantially pure compound defined according to the structure: ##STR3## and the use thereof for augmenting or enhancing the aroma or taste of consumable material ...


5
Richard M Boden, Manfred H Vock, Theodore J Tyszkiewicz: Prenyl methyl carbonate and organoleptic uses thereof. International Flavors & Fragrances, Arthur L Liberman, June 12, 1984: US04454111 (10 worldwide citation)

Processes and compositions are described for use in foodstuff, chewing gum, toothpaste and medicinal product flavor and aroma augmenting, modifying, enhancing and imparting compositions and as foodstuffs, chewing gums, toothpastes and medicinal product aroma imparting materials of prenyl methyl carb ...


6
Richard M Boden, Michael Licciardello, Theodore J Tyszkiewicz: Process for augmenting or enhancing the aroma of perfume compositions and colognes utilizing alkyl, aralkyl, and bicycloalkyl methyl carbonates. International Flavors & Fragrances, Arthur L Liberman, June 28, 1983: US04390463 (6 worldwide citation)

Described are the alkyl, aralkyl, alkadienyl and bicycloalkyl methyl carbonates defined according to the structure: ##STR1## wherein R represents 2-ethyl hexyl, having the structure: ##STR2## linalyl having the structure: ##STR3## isobornyl having the structure: ##STR4## or 1-phenylethyl having the ...


7
Richard M Boden, Theodore J Tyszkiewicz, Michael Licciardello: Branched chain alkenyl methyl carbonates, uses thereof in augmenting or enhancing the aroma of perfume compositions, colognes and perfumed articles and formate intermediates useful in preparing same. International Flavors & Fragrances, Arthur L Liberman, July 26, 1983: US04395370 (6 worldwide citation)

Described are branched chain alkenyl methyl carbonates and branched chain alkenyl formates defined according to the structure: ##STR1## wherein R.sub.3 represents hydrogen or methoxy and wherein in each of the molecules described by the structure, one of the dashed lines is a carbon-carbon double bo ...


8

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Richard M Boden, Michael Licciardello, Theodore J Tyszkiewicz: 2-Ethyl hexyl and isobornyl methyl carbonates. International Flavors & Fragrances, Arthur L Liberman, May 8, 1984: US04447365 (5 worldwide citation)

Described are the alkyl and bicycloalkyl methyl carbonates defined according to the structure: ##STR1## wherein R represents 2-ethyl hexyl, having the structure: ##STR2## or isobornyl having the structure: ##STR3## and uses thereof in augmenting or enhancing the aroma of perfume compositions, cologn ...


10
Richard M Boden, Theodore J Tyszkiewicz, Michael Licciardello, Manfred H Vock, Joaquin F Vinals, Patrick Whalen, Marie R Hanna: Flavoring with heliotropyl methyl carbonate. International Flavors & Fragrances, Arthur L Liberman, February 7, 1984: US04430354 (5 worldwide citation)

Described is a genus of compounds defined according to the structure: ##STR1## (Z) represents one of the moieties ##STR2## as well as the substantially pure compound defined according to the structure: ##STR3## and the use thereof for augmenting or enhancing the aroma or taste of consumable material ...