MILLENNIUM PHARMACEUTICALS, INC. - , US Lloyd J. Payne - Cambridge, GB Richard J. Boyce - Boxworth, GB Todd B. Sells - Bellingham MA, US Stephen G. Stroud - Medford MA, US Stuart Travers - Meppershall, GB Tricia J. Vos - Medford MA, US Gabriel S. Weatherhead - Cambridge MA, US
Assignee:
MILLENNIUM PHARMACEUTICALS, INC. - Cambridge MA
International Classification:
C07D 487/04
US Classification:
540578
Abstract:
This invention relates to compounds and methods for the treatment of cancer. In particular, the invention provides compounds that inhibit Aurora kinase, pharmaceutical compositions comprising the compounds, and methods of using the compounds for the treatment of cancer.
Jurgen M. Grasshoff - Hudson MA John L. Marshall - Somerville MA Richard A. Minns - Arlington MA Socorro M. Ramos - North Andover MA Stephen G. Stroud - Medford MA Stephen J. Telfer - Arlington MA Haixin Yang - Durham NC Roger A. Boggs - Wayland MA Eric S. Kolb - Acton MA
Assignee:
Polaroid Corporation - Cambridge MA
International Classification:
G03C 1492 G03C 1494 G03C 176
US Classification:
4302701
Abstract:
A process for generation of acid uses a medium comprising a first acid-generating component capable of generating a first acid, and a secondary acid generator, this secondary acid generator being capable of thermal decomposition to form a secondary acid, the thermal decomposition of the secondary acid generator being catalyzed by the first acid. At least part of the medium is exposed to so as to cause formation of the first acid from the first acid-generating component; and the medium is then heated to cause, in the exposed part of the medium, acid-catalyzed thermal decomposition of the secondary acid generator and formation of the secondary acid. The secondary acid generator has a first site bearing a first leaving group and a second site bearing a second leaving group, the first leaving group being capable of protonation by the first acid, with expulsion of the first leaving group to form a cation which electrophilically adds to an unsaturated reagent bearing a proton at the site of addition and a proton-containing nucleophilic grouping at an adjacent site, following which said proton on the reagent is lost and the second leaving group is displaced by said nucleophilic grouping, the second leaving group, in combination with a proton, forming the secondary acid. Preferred variants of the process are of the types described in U. S. Pat. Nos. 5,286,612; 5,334,489; 5,395,736; 5,441,850 and 5,453,345.
Roger A. Boggs - Wayland MA Jurgen M. Grasshoff - Hudson MA Eric S. Kolb - Ipswich MA John L. Marshall - Somerville MA Richard A. Minns - Arlington MA Socorro M. Ramos - North Andover MA Stephen G. Stroud - Medford MA Stephen J. Telfer - Arlington MA Haixin Yang - Norwood MA
Assignee:
Polaroid Corporation - Cambridge MA
International Classification:
C03C 1492 C03C 1494 C03C 176
US Classification:
4302701
Abstract:
A process for generation of acid uses a medium comprising a first acid-generating component capable of generating a first acid, and a secondary acid generator, this secondary acid generator being capable of thermal decomposition to form a secondary acid, the thermal decomposition of the secondary acid generator being catalyzed by the first acid. At least part of the medium is exposed to so as to cause formation of the first acid from the first acid-generating component; and the medium is then heated to cause, in the exposed part of the medium, acid-catalyzed thermal decomposition of the secondary acid generator and formation of the secondary acid. The secondary acid generator has a first site bearing a first leaving group and a second site bearing a second leaving group, the first leaving group being capable of protonation by the first acid, with expulsion of the first leaving group, followed by loss of a proton from the secondary acid generator to form an unstable intermediate, which then fragments with loss of the second leaving group, accompanied by either (a) loss of a second proton; or (b) addition of a proton-containing nucleophile, followed by loss of a proton, the second leaving group, in combination with a proton, forming the secondary acid. Preferred variants of the process are of the types described in U. S. Pat. Nos. 5,286,612; 5,334,489; 5,395,736; 5,441,850 and 5,453,345.
Benzpyrylium Squarylium And Croconylium Dyes, And Processes For Their Preparation And Use
Peter K. Chu - Acton MA Serajul Haque - Braintree MA Anthony J. Puttick - Arlington MA Socorro M. Ramos - Belmont MA Robert P. Short - Arlington MA Stephen G. Stroud - Medford MA Stephen J. Telfer - Arlington MA Michael J. Zuraw - Arlington MA
Assignee:
Polaroid Corporation - Cambridge MA
International Classification:
C07D34500 C07D33504 C07D31104
US Classification:
540 1
Abstract:
Dyes comprising an inner salt of a compound of the formula: Q. sup. 1 =Z-Q. sup. 2 wherein: Q. sup. 1 is a 4-(benz[b]-4H-pyrylium)methylidene, 4-(benz[b]-4H-thiopyrylium)methylidene or 4-(benz[b]-4H-selenopyrylium)methylidene grouping; Z is a 1,3-(2-hydroxy-4-oxo-2-cyclobutylidene) hydroxide or 1,3-(2-hydroxy-4,5-dioxo-2-cyclopentylidene) hydroxide ring; and Q. sup. 2 is a 4-(benz[b]-4H-pyran-4-ylidene)methyl, 4-(benz[b]-4H-thiopyran-4-ylidene)methyl or 4-(benz[b]-4H-selenopyran-4-ylidene)methyl grouping; wherein at least one of the groupings Q. sup. 1 and Q. sup. 2 carries at its 2-position a substituent in which a non-aromatic carbon atom is bonded directly to the benzpyrylium, benzthiopyrylium or benzselenopyrylium nucleus, subject to the proviso that if this 2-substituent contains an aromatic nucleus, this aromatic nucleus is not conjugated with the benzpyrylium, benzthiopyrylium or benzselenopyrylium nucleus to which it is attached, are useful as visible and near infra-red absorbers, having high extinction coefficients and improved solubility in polymeric media.
Chrome Complexed Dye Developer Compounds And Photographic Products And Processes
Patrick F. King - Needham MA Stephen G. Stroud - Brighton MA
Assignee:
Polaroid Corporation - Cambridge MA
International Classification:
G03C 140 G03C 554 G03C 700 C09B 4500
US Classification:
430225
Abstract:
Novel chrome complexed azo and azomethine yellow dye developers which include a substantially colorless symmetrical ligand. Also disclosed are photographic products and processes which utilize the dye developers.
Benzpyrylium Squarylium And Croconylium Dyes, And Processes For Their Preparation And Use
Peter K. Chu - Acton MA Serajul Haque - Braintree MA Anthony J. Puttick - Arlington MA Socorro M. Ramos - Belmont MA Robert P. Short - Arlington MA Stephen G. Stroud - Medford MA Stephen J. Telfer - Arlington MA Michael J. Zuraw - Arlington MA
Assignee:
Polaroid Corporation - Cambridge MA
International Classification:
G03C 1725 G03C 1735 G03C 173
US Classification:
430332
Abstract:
Dyes comprising an inner salt of a compound of the formula: Q. sup. 1 =Z-Q. sup. 2 wherein: Q. sup. 1 is a 4-(benz[b]-4H-pyrylium)methylidene, 4-(benz[b]-4H-thiopyrylium)methylidene or 4-(benz[b]-4H-selenopyrylium)methylidene grouping; Z is a 1,3-(2-hydroxy-4-oxo-2-cyclobutylidene) hydroxide or 1,3-(2-hydroxy-4,5-dioxo-2-cyclopentylidene) hydroxide ring; and Q. sup. 2 is a 4-(benz[b]-4H-pyran-4-ylidene)methyl, 4-(benz[b]-4H-thiopyran-4-ylidene)methyl or 4-(benz[b]-4H-selenopyran-4-ylidene)methyl grouping; wherein at least one of the groupings Q. sup. 1 and Q. sup. 2 carries at its 2-position a substituent in which a non-aromatic carbon atom is bonded directly to the benzpyrylium, benzthiopyrylium or benzselenopyrylium nucleus, subject to the proviso that if this 2-substituent contains an aromatic nucleus, this aromatic nucleus is not conjugated with the benzpyrylium, benzthiopyrylium or benzselenopyrylium nucleus to which it is attached, are useful as visible and near infra-red absorbers, having high extinction coefficients and improved solubility in polymeric media.
Jurgen M. Grasshoff - Hudson MA John L. Marshall - Somerville MA Richard A. Minns - Arlington MA Socorro M. Ramos - North Andover MA Stephen G. Stroud - Medford MA Stephen J. Telfer - Arlington MA Haixin Yang - Norwood MA Roger A. Boggs - Wayland MA Eric S. Kolb - Acton MA
Assignee:
Polaroid Corporation - Cambridge MA
International Classification:
C07F 902
US Classification:
558208
Abstract:
A process for generation of acid uses a medium comprising a first acid-generating component capable of generating a first acid, and a secondary acid generator, this secondary acid generator being capable of thermal decomposition to form a secondary acid, the thermal decomposition of the secondary acid generator being catalyzed by the first acid. At least part of the medium is exposed to so as to cause formation of the first acid from the first acid-generating component; and the medium is then heated to cause, in the exposed part of the medium, acid-catalyzed thermal decomposition of the secondary acid generator and formation of the secondary acid. The secondary acid generator has a first site bearing a first leaving group and a second site bearing a second leaving group, the first leaving group being capable of protonation by the first acid, with expulsion of the first leaving group to form a cation which electrophilically adds to an unsaturated reagent bearing a proton at the site of addition and a proton-containing nucleophilic grouping at an adjacent site, following which said proton on the reagent is lost and the second leaving group is displaced by said nucleophilic grouping, the second leaving group, in combination with a proton, forming the secondary acid. Preferred variants of the process are of the types described in U. S. Pat. Nos. 5,286,612; 5,334,489; 5,395,736; 5,441,850 and 5,453,345.
Patrick F. King - Needham MA Stephen G. Stroud - Brighton MA
Assignee:
Polaroid Corporation - Cambridge MA
International Classification:
G03C 554 G03C 142
US Classification:
430441
Abstract:
Novel compounds which are capable of forming a coordination complex with a metal and which include a silver halide developing substituent or a precursor thereof. The compounds are useful as silver halide developing agents and as intermediates for dye developers which are utilized in photographic applications.
John J Duggan Academy and John F Kennedy Academy
Academic Director
John J Duggan Academy
Dean of Curriculum and Instruction
John J Duggan Academy
Expeditionary Learning Magnet Resource Teacher
S.t.e.m Middle Academy Aug 2009 - Jun 2014
Expeditionary Learning Magnet Resource Teacher
The Leadership School at Kieve Mar 2008 - Mar 2009
Director
Education:
Lesley University 1996 - 1998
Master of Science, Masters, Education
Hobart and William Smith Colleges 1989 - 1993
Bachelors, Bachelor of Arts, Mathematics
Skills:
Curriculum Design Curriculum Development Classroom Teaching Educational Leadership Teacher Training Tutoring Educational Technology Instructional Design Staff Development Non Profits Grant Writing Program Development Community Outreach Lesson Planning Editing Secondary Education Elementary Education Curriculum Mapping Volunteer Management Coaching Event Planning Program Evaluation Project Based Learning Science Curriculum Assessment Science Education Professional Learning Communities Powerpoint Smartboard Workshop Facilitation Conflict Resolution Classroom Management Instructional Technology Gifted Education Technology Integration Educational Consulting Differentiated Instruction Adult Education International Education K 12 Nonprofits