1
James O Bledsoe, Michael Britten Kelly, Mark A Sprecker, Robert P Belko, Manfred Pawlak, Michael G Monteleone: Fruity musk compositions. International Flavors & Fragrances, Joseph F Leightner, July 19, 2005: US06919477 (10 worldwide citation)

Novel ester compounds and the use of these esters as a fragrance chemicals, suitable for use in creating fragrance, and scents in items such as perfumes, colognes and personal care products are disclosed.


2
James O Bledsoe, Michael Britten Kelly, Mark A Sprecker, Robert P Belko, Manfred Pawlak, Michael G Monteleone: Fruity musk compositions. International Flavors & Fragrances, Joseph F Leightner, August 10, 2004: US06774260 (10 worldwide citation)

Novel ester compounds and the use of these esters as a fragrance chemicals, suitable for use in creating fragrance, and scents in items such as perfumes, colognes and personal care products are disclosed.


3
Richard L Veazey, James O Bledsoe Jr: Adhesive compositions. Union Camp Corporation, Kane Dalsimer Kane Sullivan and Kurucz, March 17, 1987: US04650822 (8 worldwide citation)

Terpene ethers are found to be advantageous tackifiers in elastomeric resin based adhesives.


4
James O Bledsoe Jr, Walter E Johnson Jr: Substituted cyclopropane process and product. SCM Corporation, Jerry K Mueller Jr, June 27, 1978: US04097531 (7 worldwide citation)

Substituted cyclopropyl ketones can be made by heating unsaturated halo-ketones in the presence of alkaline earth metal carbonate and liquid glycol vehicle.


5
James O Bledsoe Jr, Carlos G Cardenas: Hydrogenation process for the selective preparation of 3-menthene. SCM Corporation, Merton H Douthitt, Jerry K Mueller Jr, May 20, 1980: US04204080 (2 worldwide citation)

Non-conjugated para-menthadienes having one site of unsaturation at the 4(8)- or 8-position are hydrogenated to selectively form 3-menthene in the presence of a homogeneous ruthenium catalyst complex.


6
James O Bledsoe Jr, Carlos G Cardenas: Selective conversion of d-isolimonene to d-3-menthene. SCM Corporation, A J Gibbons, February 3, 1981: US04249028 (1 worldwide citation)

d-3-Menthene of high optical purity is obtained by the selective isomerization/hydrogenation of d-isolimonene in the presence of minor amounts of a palladium catalyst at temperatures up to 200.degree. C. and pressures of preferably about 100-500 psig.


7
Bernard J Kane, Karen E Irving, James O Bledsoe Jr, Levy A Canova: Hydrogenation of cyclic unsaturated compounds. SCM Corporation, Richard H Thomas, November 15, 1977: US04058572 (1 worldwide citation)

In a process for hydrogenation, with elemental hydrogen gas in the presence of a hydrogenation catalyst, of a cyclic unsaturated compound having an hydroxyl group projecting from an asymmetric center of the ring and an olefinic carbon-to-carbon double bond which when saturated in the hydrogenation p ...


8
James O Bledsoe Jr, Bernard Brust: Process for purifying exo-2-hydroxy-1,4 cineole. Union Camp Corporation, Edward J Sites, August 1, 1989: US04853089

A process for purifying exo-2-hydroxy-1,4-cineole contaminated with ketones is carried out by derivatizing the ketone to form a compound readily separable from the desired cineole, either by distillation, solvent extraction or like separation process. In one embodiment method of the invention, deriv ...


9
James O Bledsoe, Michael Britten Kelly, Mark A Sprecker, Robert P Belko, Manfred Pawlak, Michael G Monteleone: Fruity musk compositions. Joseph F Leightner Esq, International Flavors & Fragrances, October 28, 2004: US20040214745-A1

Novel ester compounds and the use of these esters as a fragrance chemicals, suitable for use in creating fragrance, and scents in items such as perfumes, colognes and personal care products are disclosed.


10
James O Bledsoe, Michael Britten Kelly, Mark A Sprecker, Robert P Belko, Manfred Pawlak, Michael G Monteleone: Fruity musk compositions. Joseph F Leightner Esq, International Flavors & Fragrances, March 18, 2004: US20040053811-A1

Novel ester compounds and the use of these esters as a fragrance chemicals, suitable for use in creating fragrance, and scents in items such as perfumes, colognes and personal care products are disclosed.