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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, Michael Licciardello, Joseph J Maisano Jr, Marie R Hanna: Perfumed stable aqueous hypochlorite bleach compositions containing 2-methyl-2-octanol and thickened variation thereof. International Flavors & Fragrances, Arthur L Liberman, June 28, 1983: US04390448 (24 worldwide citation)

Described is a process for producing a stable single phase aqueous alkali metal hypochlorite solution having good surface tension properties and optionally having a relatively high viscosity (5-25 centipoises at 20.degree.-40.degree. C.) and having a stable fragrance consisting, in sequential order, ...


3
Mark A Sprecker, Robert P Belko, Richard M Boden, Marie R Hanna: Beta-alkylidene phenethyl alcohol esters and ethers, organoleptic uses thereof and processes for preparing same. International Flavors & Fragrances, Arthur L Liberman, September 20, 1988: US04772583 (14 worldwide citation)

Described is the novel compound genus the beta-alkylidene phenethyl alcohol esters and ethers of our invention defined according to the generic structure: ##STR1## wherein R.sub.5 represents hydrogen or methyl; wherein R.sub.6 represents one of the moieties: ##STR2## wherein R.sub.1, R.sub.2, R.sub. ...


4
Mark A Sprecker, Richard A Weiss, Anthony T Levorse Jr, Howard H Heinsohn Jr, Charles E J Beck, Marie R Hanna: Carbon containing functional group substituted 4,5,6,7-tetrahydro-polyalkylated-4-indanes, isomers thereof, processes for preparing same and uses thereof. International Flavors & Fragrances, Joseph F Leightner, August 7, 2001: US06271193 (13 worldwide citation)

Described are carbon-containing functional groups substituted 4,5,6,7-tetrahydro-polyalkylated-4-indanes, isomers thereof, process for processes for preparing same, and uses thereof. The 4,5,6,7-tetrahydro-polyalkylated-4-indanes have the generic structure:


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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 ...


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Mark A Sprecker, Robert P Belko, Salvatore M Brucato, Charles E J Beck, Marie R Hanna: 2,4-disubstituted and 2,2,4-trisubstituted tetrahydropyranyl-4-ethers, process for preparing same and perfumery uses thereof. International Flavors & Fragrances, Arthur L Liberman, October 9, 1990: US04962090 (10 worldwide citation)

Described are 2,4-disubstituted and 2,2,4-trisubstituted tetrahydropyranyl-4-ethers defined according to the generic structure: ##STR1## wherein R' represents methyl or ethyl; R.sub.1 and R.sub.2 taken alone are the same or different hydrogen, phenyl, C.sub.1 -C.sub.8 alkyl or C.sub.2 -C.sub.8 alken ...


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William Gillaspey, Myrna L Hagedorn, Marie R Hanna, Kathleen E Boardwick, Charles E J Beck, Futoshi Fujioka, Anthony G Branco, Anubhav Narula, Richard M Boden: Adamantane derivatives, compositions of matter containing same, processes for preparing said adamantane derivatives and said compositions, and organoleptic and deodorancy uses of said adamantane derivatives and said compositions. International Flavors & Fragrances, Arthur L Liberman, June 4, 1991: US05021184 (8 worldwide citation)

Described are adamantane derivatives defined according to the generic structure: ##STR1## wherein R.sub.1 ' is hydrogen or acetyl; R.sub.2 ' is hydrogen or lower alkyl and the dashed line is a carbon-carbon single bond or a carbon-carbon double bond as well as uses thereof for augmenting or enhancin ...


10
Richard M Boden, Futoshi Fujioka, Marie R Hanna: Fragrance use of dihydromethyl jasmonic acid. International Flavors & Fragrances, Arthur L Liberman, April 5, 1994: US05300489 (8 worldwide citation)

Described in the use of dihydromethyl jasmonic acid having the structure: ##STR1## in augmenting, enhancing or imparting fragrances in or to perfume compositions, perfumed articles and colognes.