PAUL B. REESE

Paul B. Reese

1. http://www.sciencedirect.com/science/article/pii/S0039128X07000943
Steroids
Volume 72, Issues 9–10, September 2007, Pages 713–722
Steroid hydroxylation by Whetzelinia sclerotiorum, Phanerochaete chrysosporium and Mucor plumbeus
DEDICATION: Dedicated to Professor Sir John Cornforth, University of Sussex, as he celebrates his 90th birthday.
Andrew S. Lamma, Avril R.M. Chena, William F. Reynoldsb, Paul B. Reesea, ,
a Department of Chemistry, University of the West Indies, Mona, Kingston 7, Jamaica
b Department of Chemistry, University of Toronto, Toronto, Ontario, Canada M5S 3H6
http://dx.doi.org/10.1016/j.steroids.2007.05.008, How to Cite or Link Using DOI
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2. http://www.sciencedirect.com/science/article/pii/S0031942205002979
Phytochemistry
Volume 66, Issue 16, August 2005, Pages 1898–1902
Stemodane and stemarane diterpenoid hydroxylation by Mucor plumbeus and Whetzelinia sclerotiorum
Dedicated to the memory of Professor Herbert L. Holland (Brock University) for his contribution to Bio-organic Chemistry for over 30 years.
Avril R.M. Chena, Peter L.D. Ruddocka, Andrew S. Lamma, William F. Reynoldsb, Paul B. Reesea, a Department of Chemistry, University of the West Indies, Mona, Kingston 7, Jamaica
b Department of Chemistry, University of Toronto, Toronto, Ont., Canada M5S 3H6
http://dx.doi.org/10.1016/j.phytochem.2005.06.015, How to Cite or Link Using DOI
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3. http://pubs.acs.org/doi/abs/10.1021/jf050008y
Biological Activity and Chemical Composition of the Essential Oil from Jamaican Hyptis verticillata Jacq.
AbstractFull Text HTMLHi-Res PDF[42 KB]Supporting Info ->FiguresCiting Articles
Petrea C. Facey ,† Roy B. R. Porter ,*† Paul B. Reese ,† and Lawrence A. D. Williams §
Department of Chemistry, University of the West Indies, Mona, Kingston 7, Jamaica, and Scientific Research Council, Old Hope Road, Kingston 6, Jamaica
J. Agric. Food Chem., 2005, 53 (12), pp 4774–4777
DOI: 10.1021/jf050008y
Publication Date (Web): May 21, 2005
Copyright © 2005 American Chemical Society

Abstract
The chemical composition of the essential oil obtained by hydrodistillation from the aerial parts of Hyptis verticillata Jacq. was elucidated by a combination of GC and GC-MS analyses. The oil was dominated by the sesquiterpenoids cadina-4,10(15)-dien-3-one (15.1%) (1) and aromadendr-1(10)-en-9-one (squamulosone) (30.7%) (2). The oil exhibited chemosterilant activities against the cattle tick, Boophilus microplus Canest., and toxic action against adult Cylas formicarius elegantulus Summer, the most destructive pest of sweet potato (Ipomoea species).
Keywords: Hyptis verticillata; Labiatae; essential oil; sesquiterpene; Boophilus microplus; Cylas formicarius elegantulus; GC-MS; GC

4. http://www.sciencedirect.com/science/article/pii/S0031942204000238
Phytochemistry
Volume 65, Issue 6, March 2004, Pages 701–710
Investigation of the importance of the C-2 oxygen function in the transformation of stemodin analogues by Rhizopus oryzae ATCC 11145
Dedicated to the memory of Professor Herbert L. Holland (Brock University) for his contribution to Bio-organic Chemistry over more than 30 years.
Glenroy D.A. Martina, William F. Reynoldsb, Paul B. Reesea, ,
a Department of Chemistry, University of the West Indies, Mona, Kingston 7, Jamaica
b Department of Chemistry, University of Toronto, Toronto, Ontario, Canada M5S 3H6
http://dx.doi.org/10.1016/j.phytochem.2004.01.011, How to Cite or Link Using DOI
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5. http://pubs.acs.org/doi/abs/10.1021/np0303299
New Cembranes from Cleome spinosa
AbstractFull Text HTMLHi-Res PDF[60 KB]PDF w/ Links[102 KB]FiguresCiting Articles
Dwight O. Collins ,† William F. Reynolds ,*‡ and Paul B. Reese *†
Department of Chemistry, University of the West Indies, Mona, Kingston 7, Jamaica, West Indies, and Department of Chemistry, University of Toronto, Toronto, Ontario, Canada M5S 1A1
J. Nat. Prod., 2004, 67 (2), pp 179–183
DOI: 10.1021/np0303299
Publication Date (Web): December 3, 2003
Copyright © 2004 American Chemical Society and American Society of Pharmacognosy

Abstract
Examination of the aerial portions of Cleome spinosa yielded five new cembranes, named cleospinols A (1), B (3), C (4), and D (5), and the 3‘-hydroxy-iso-pentan-10-oate ester of cleospinol A (2). The cleospinols were determined to be derivatives of 10,13-dihydroxy-4,12-dimethyl-1-(1-methylethenyl)-11(E)-cyclotetradecene on the basis of spectroscopic data interpretation.

6. http://www.sciencedirect.com/science/article/pii/S003194220600207X
Phytochemistry
Volume 67, Issue 11, June 2006, Pages 1088–1093
Bioconversion of Stemodia maritima diterpenes and derivatives by Cunninghamella echinulata var. elegans and Phanerochaete chrysosporium
Andrew S. Lamma, William F. Reynoldsb, Paul B. Reesea, ,
a Department of Chemistry, University of the West Indies, Mona, Kingston 7, Jamaica
b Department of Chemistry, University of Toronto, Toronto, Ont., Canada M5S 3H6
http://dx.doi.org/10.1016/j.phytochem.2006.04.001, How to Cite or Link Using DOI
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7. http://www.sciencedirect.com/science/article/pii/S003194220500083X
Phytochemistry
Volume 66, Issue 8, April 2005, Pages 901–909
Stemodane skeletal rearrangement: chemistry and microbial transformation
Dedicated to the memory of Professor Herbert L. Holland (Brock University) for his contribution to Bio-organic Chemistry for over 30 years
Glenroy D.A. Martina, William F. Reynoldsb, Paul B. Reesea, ,
a Department of Chemistry, University of the West Indies, Mona, Kingston 7, Jamaica
b Department of Chemistry, University of Toronto, Toronto, Ont., Canada M5S 3H6
http://dx.doi.org/10.1016/j.phytochem.2005.02.019, How to Cite or Link Using DOI
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8. http://www.sciencedirect.com/science/article/pii/S0031942201004873
Phytochemistry
Volume 59, Issue 5, March 2002, Pages 489–492
Biotransformation of cadina-4,10(15)-dien-3-one and 3α-hydroxycadina-4,10(15)-diene by Curvularia lunata ATCC 12017
Dwight O Collins, Paul B Reese,
Department of Chemistry, University of the West Indies, Mona, Kingston 7, Jamaica
http://dx.doi.org/10.1016/S0031-9422(01)00487-3, How to Cite or Link Using DOI
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9. http://www.sciencedirect.com/science/article/pii/S0031942204002328
Phytochemistry
Volume 65, Issue 15, August 2004, Pages 2211–2217
Investigation of the importance of the C-2 and C-13 oxygen functions in the transformation of stemodin analogues by Rhizopus oryzae ATCC 11145
Dedicated to the memory of Professor Herbert L. Holland (Brock University) for his contribution to Bio-organic Chemistry for over 30 years
Glenroy D.A. Martina, William F. Reynoldsb, Paul B. Reesea, ,
a Department of Chemistry, University of the West Indies, Mona, Kingston 7, Jamaica
b Department of Chemistry, University of Toronto, Toronto, Ont., Canada M5S 3H6
http://dx.doi.org/10.1016/j.phytochem.2004.05.016, How to Cite or Link Using DOI
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10. http://www.sciencedirect.com/science/article/pii/S0039128X04000108
Steroids
Volume 69, Issue 3, March 2004, Pages 193–199
The reactions of palladium(II), thallium(III) and lead(IV) trifluoroacetates with 3β-acetoxyandrost-5-en-17-one: crystal structure of the first trifluoroacetate bridged 5,6,7-π-allyl steroid palladium dimer
Dedicated to the memory of Professor Herbert L. Holland (Brock University) for his contribution to Bio-organic Chemistry over more than 30 years
Peter L Ruddocka, David J Williamsb, Paul B Reesea, ,
a Chemistry Department, University of the West Indies, Mona, Kingston 7, Jamaica
b Chemical Crystallography Laboratory, Chemistry Department, Imperial College of Science, Technology and Medicine, South Kensington, London SW7 2AY, UK
http://dx.doi.org/10.1016/j.steroids.2004.01.001, How to Cite or Link Using DOI
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11.
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