S. Chow

发表

EBC-232 and 323: A Structural Conundrum Necessitating Unification of Five In Silico Prediction and Elucidation Methods.

P. Parsons, Carly J. Pierce, G. Boyle, 2020, Chemistry.

Synthetic Tigliane Intermediates Engage Thiols to Induce Potent Cell Line Selective Anti-Cancer Activity.

P. Parsons, G. Boyle, Mingzhao Zhu, 2020, Chemistry.

En Route to D-Ring Inverted Phorbol Esters.

S. Chow, Craig M. Williams, P. Bernhardt, 2019, Organic letters.

sp-sp3 coupling reactions of alkynylsilver cations, RC≡CAg2+ (R = Me and Ph) with allyliodide.

S. Chow, Craig M. Williams, R. O'hair, 2013, Dalton transactions.

Insect chemistry and chirality.

W. Kitching, Y. Tu, M. McGrath, 2003, Chirality.

Herbicides to control poisonous Pimelea species (Thymelaeaceae)

J. Vitelli, S. Chow, R. Silcock, 2012 .

Direct Observation of an Oxepin from a Bacterial Cytochrome P450-Catalyzed Oxidation.

R. Poirier, E. Krenske, S. Chow, 2016, Chemistry.

Substrate analog studies of the ω-regiospecificity of Mycobacterium tuberculosis cholesterol metabolizing cytochrome P450 enzymes CYP124A1, CYP125A1 and CYP142A1.

P. Ortiz de Montellano, S. Chow, Arti Singh, 2012, Bioorganic & medicinal chemistry.

Synthesis of l-indospicine, [5,5,6-(2)H3]-l-indospicine and l-norindospicine.

M. Fletcher, S. Chow, J. Ng, 2016, Organic & biomolecular chemistry.

Synthesis of the seco-Limonoid BCD Ring System Identifies a Hsp90 Chaperon Machinery (p23) Inhibitor.

L. Guddat, G. P. Savage, S. Chow, 2018, Chemistry.

Organocatalytic Asymmetric Michael Addition of 2,2‐Dimethyl‐1,3‐dioxan‐5‐one to Nitro Alkenes Employing Proline‐Based Catalysts

D. Enders, S. Chow, 2006 .

Unearthing the Subtleties of Rhodium(II)-Catalyzed Carbenoid Cycloadditions to Furans with an N-Sulfonyl-1,2,3-triazole Probe.

S. Chow, Craig M. Williams, H. Davies, 2022, Organic letters.

Hydrolytic kinetic resolution of terminal mono- and bis-epoxides in the synthesis of insect pheromones: routes to (−)-(R)- and (+)-(S)-10-methyldodecyl acetate, (−)-(R)-10-methyl-2-tridecanone, (−)-(R)-(Z)-undec-6-en-2-ol (Nostrenol), (−)-(1R,7R)-1,7-dimethylnonyl propanoate, (−)-(6R,12R)-6,12-dimet

W. Kitching, S. Chow, 2002 .

Hydrolytic kinetic resolution of mono- and bisepoxides as a key step in the synthesis of insect pheromones

W. Kitching, S. Chow, 2001 .

CH and CC bond activation reactions in silver alkynyl cluster cations, RCCAg2+

S. Chow, Craig M. Williams, R. O'hair, 2013 .

Rhodium-Catalyzed [4+3] Cycloaddition to Furans: Direct Access to Functionalized Bicyclo[5.3.0]decane Derivatives

P. Parsons, G. Boyle, S. Chow, 2016 .

Elucidating the mechanism of the Ley–Griffith (TPAP) alcohol oxidation† †Electronic supplementary information (ESI) available. See DOI: 10.1039/c7sc04260d

S. Chow, Craig M. Williams, P. Bernhardt, 2017, Chemical science.

Synthesis and Enantioselective Gas Chromatography of Stereoisomers of 7,11‐Dimethylheptadecane − A Pheromone Component of Lambdina Species

W. Kitching, S. Chow, W. Koenig, 2004 .

Daphnane- and tigliane-type diterpenoid esters and orthoesters from Pimelea elongata.

M. Fletcher, S. Chow, P. Hayes, 2010, Journal of natural products.

Pimelotides A and B, diterpenoid ketal-lactone orthoesters with an unprecedented skeleton from Pimelea elongata.

M. Fletcher, S. Chow, P. Hayes, 2009, Journal of natural products.

Novel cuticular hydrocarbons from the cane beetle Antitrogus parvulus--4,6,8,10,16-penta- and 4,6,8,10,16,18-hexamethyldocosanes-unprecedented anti-anti-anti-stereochemistry in the 4,6,8,10-methyltetrad.

W. Kitching, P. Allsopp, C. Moore, 2005, The Journal of organic chemistry.

4,6,8,10,16-penta- and 4,6,8,10,16,18-hexamethyldocosanes from the cane beetle antitrogusparvulus--cuticular hydrocarbons with unprecedented structure and stereochemistry.

W. Kitching, P. Allsopp, C. Moore, 2003, Organic letters.

Diverse cuticular hydrocarbons from Australian canebeetles (Coleoptera: Scarabaeidae)

W. Kitching, M. McGrath, P. Allsopp, 2008 .

Determining a synthetic approach to pierisformaside C.

S. Chow, Craig M. Williams, C. Kress, 2011, Organic letters.

Synthesis of the sponge-derived plakortone series of bioactive compounds.

W. Kitching, S. Chow, P. Bernhardt, 2010, The Journal of organic chemistry.

Ranking Oxidant Sensitiveness: A Guide for Synthetic Utility.

M. Johnston, S. Chow, Craig M. Williams, 2019, Chemistry.

EBC-342: A Novel Tetrahydrofuran Moiety Containing Casbane from the Australian Rainforest

P. Parsons, Carly J. Pierce, G. Boyle, 2020 .

Novel Sesquiterpenes from the Fungus Lactarius piperatus

W. Kitching, Ying Wang, S. Chow, 2003 .

Title The use of optical coherence tomography in the assessment ofdiabetic retinopathy and maculopathy

Raymond, S. Chow, Wong, 2022 .

seco-Pregnane Glycosides from Australian Caustic Vine (Cynanchum viminale subsp. australe).

G. Boyle, Hieng C Lu, K. Fischer, 2023, Journal of natural products.

Significance of Protein-Substrate Hydrogen Bonding for the Selectivity of P450-Catalysed Oxidations.

S. Chow, J. D. De Voss, Kate E. Slessor, 2019, Chemistry.

Direct Observation of an Oxepin from a Bacterial Cytochrome P450-Catalyzed Oxidation.

Jeanette E. Stok, R. Poirier, E. Krenske, 2016, Chemistry.