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William Martin - Publications

Affiliations: 
2001-2005 Chemistry University of Nottingham, Nottingham, England, United Kingdom 
 2006-2007 Oregon State University, Corvallis, OR 
 2009- Chemistry University of Bradford, Bradford, England, United Kingdom 
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13 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2008 White JD, Demnitz FW, Xu Q, Martin WH. Synthesis of an advanced intermediate for (+)-pillaromycinone. Staunton-Weinreb annulation revisited. Organic Letters. 10: 2833-6. PMID 18537256 DOI: 10.1021/Ol8009732  0.381
2008 White JD, Lincoln CM, Yang J, Martin WH, Chan DB. Total synthesis of solandelactones A, B, E, and F exploiting a tandem Petasis-Claisen lactonization strategy. The Journal of Organic Chemistry. 73: 4139-50. PMID 18452338 DOI: 10.1021/Jo800335G  0.625
2007 White JD, Martin WH, Lincoln C, Yang J. Total synthesis of solandelactones E and F, homoeicosanoids from the hydroid Solanderia secunda. Organic Letters. 9: 3481-3. PMID 17658844 DOI: 10.1021/Ol701564X  0.632
2007 Clarke PA, Santos S, Martin WHC. Combining pot, atom and step economy (PASE) in organic synthesis. Synthesis of tetrahydropyran-4-ones Green Chemistry. 9: 438-440. DOI: 10.1039/B700923B  0.487
2005 Martin WH, Blechert S. Ring closing metathesis in the synthesis of biologically interesting peptidomimetics, sugars and alkaloids. Current Topics in Medicinal Chemistry. 5: 1521-40. PMID 16378490 DOI: 10.2174/156802605775009757  0.448
2005 Clarke PA, Martin WH, Hargreaves JM, Wilson C, Blake AJ. The one-pot, multi-component construction of highly substituted tetrahydropyran-4-ones using the Maitland-Japp reaction. Organic & Biomolecular Chemistry. 3: 3551-63. PMID 16172694 DOI: 10.1039/B508252H  0.496
2005 Clarke PA, Martin WH, Hargreaves JM, Wilson C, Blake AJ. Revisiting the Maitland-Japp reaction. Concise construction of highly functionalised tetrahydropyran-4-ones. Chemical Communications (Cambridge, England). 1061-3. PMID 15719116 DOI: 10.1039/B416247A  0.493
2005 Clarke PA, Martin WHC. Exploiting the Maitland-Japp reaction: A synthesis of (±)- centrolobine Tetrahedron. 61: 5433-5438. DOI: 10.1016/J.Tet.2005.04.011  0.464
2005 Clarke PA, Martin WHC. Exploiting the Maitland—Japp Reaction: A Synthesis of (.+-.)-Centrolobine Cheminform. 36. DOI: 10.1002/chin.200541206  0.514
2005 Clarke PA, Martin WHC. An Expedient Synthesis of (.+-.)-Centrolobine. Cheminform. 36. DOI: 10.1002/chin.200513235  0.505
2004 Clarke PA, Martin WHC. An expedient synthesis of (±)-centrolobine Tetrahedron Letters. 45: 9061-9063. DOI: 10.1016/J.Tetlet.2004.10.035  0.506
2003 Clarke PA, Martin WHC. Synthetic methods: Part (v) protecting groups Annual Reports On the Progress of Chemistry - Section B. 99: 84-103. DOI: 10.1039/B212008A  0.377
2002 Clarke PA, Martin WH. Diastereoselective synthesis of highly substituted tetrahydropyran-4-ones. Organic Letters. 4: 4527-9. PMID 12465929 DOI: 10.1021/Ol027081J  0.511
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