Xiaowen Peng, Ph.D.

Affiliations: 
2006 Ohio State University, Columbus, Columbus, OH 
Area:
organic synthesis
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"Xiaowen Peng"
Mean distance: 8.85
 
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Leo A. Paquette grad student 2006 Ohio State
 (Total synthesis of the phytopathogen (+)-fomannosin.)
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Publications

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Braun A, Cho IH, Ciblat S, et al. (2009) Enantioselective synthesis of structurally intricate and complementary polyoxygenated building blocks of spongistatin 1 (altohyrtin a) Collection of Czechoslovak Chemical Communications. 74: 651-769
Paquette LA, Peng X, Yang J, et al. (2008) The carbohydrate-sesquiterpene interface. directed synthetic routes to both (+)- and (-)-fomannosin from D-glucose. The Journal of Organic Chemistry. 73: 4548-58
Stewart CA, Peng X, Paquette LA. (2008) An efficient means for generating p-methoxybenzyl (PMB) ethers under mildly acidic conditions Synthesis. 0433-0437
Paquette LA, Peng X, Yang J. (2007) Asymmetric synthesis of the phytopathogen (+)-fomannosin. Angewandte Chemie (International Ed. in English). 46: 7817-9
O'Connor PD, Knight CK, Friedrich D, et al. (2007) Pectenotoxin-2 synthetic studies. 3. Assessment of the capacity for stereocontrolled cyclization to form the entire C1-C26 subunit based upon the double bond geometry across C15-C16. The Journal of Organic Chemistry. 72: 1747-54
Peng X, Bondar D, Paquette LA. (2005) Alkoxide Precoordination to Rhodium Enables Stereodirected Catalytic Hydrogenation of a Dihydrofuranol Precursor of the C29-40 F/G Sector of Pectenotoxin-2. Cheminform. 36
Peng X, Bondar D, Paquette LA. (2004) Alkoxide precoordination to rhodium enables stereodirected catalytic hydrogenation of a dihydrofuranol precursor of the C29-40 F/G sector of pectenotoxin-2 Tetrahedron. 60: 9589-9598
Paquette LA, Peng X, Bondar D. (2002) Pectenotoxin-2 synthetic studies. 1. Alkoxide precoordination to [Rh(NBD)(DIPHOS-4)]BF(4) allows directed hydrogenation of a 2,3-dihydrofuran-3-ol without competing furan production. Organic Letters. 4: 937-40
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