William Martin

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 
"William Martin"
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Paul A. Clarke grad student 2001-2005 Nottingham
Siegfried Blechert post-doc 2005-2006 TU Berlin
James D. White post-doc 2006-2007 Oregon State
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White JD, Demnitz FW, Xu Q, et al. (2008) Synthesis of an advanced intermediate for (+)-pillaromycinone. Staunton-Weinreb annulation revisited. Organic Letters. 10: 2833-6
White JD, Lincoln CM, Yang J, et al. (2008) Total synthesis of solandelactones A, B, E, and F exploiting a tandem Petasis-Claisen lactonization strategy. The Journal of Organic Chemistry. 73: 4139-50
White JD, Martin WH, Lincoln C, et al. (2007) Total synthesis of solandelactones E and F, homoeicosanoids from the hydroid Solanderia secunda. Organic Letters. 9: 3481-3
Clarke PA, Santos S, Martin WHC. (2007) Combining pot, atom and step economy (PASE) in organic synthesis. Synthesis of tetrahydropyran-4-ones Green Chemistry. 9: 438-440
Martin WH, Blechert S. (2005) Ring closing metathesis in the synthesis of biologically interesting peptidomimetics, sugars and alkaloids. Current Topics in Medicinal Chemistry. 5: 1521-40
Clarke PA, Martin WH, Hargreaves JM, et al. (2005) The one-pot, multi-component construction of highly substituted tetrahydropyran-4-ones using the Maitland-Japp reaction. Organic & Biomolecular Chemistry. 3: 3551-63
Clarke PA, Martin WH, Hargreaves JM, et al. (2005) Revisiting the Maitland-Japp reaction. Concise construction of highly functionalised tetrahydropyran-4-ones. Chemical Communications (Cambridge, England). 1061-3
Clarke PA, Martin WHC. (2005) Exploiting the Maitland-Japp reaction: A synthesis of (±)- centrolobine Tetrahedron. 61: 5433-5438
Clarke PA, Martin WHC. (2005) Exploiting the Maitland—Japp Reaction: A Synthesis of (.+-.)-Centrolobine Cheminform. 36
Clarke PA, Martin WHC. (2005) An Expedient Synthesis of (.+-.)-Centrolobine. Cheminform. 36
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