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2012

Journal Article

Erratum: Enantioselective total synthesis of ()-neovibsanin G and ()-14-epi-neovibsanin G (Chemical Communications (2012) (287-289) DOI: 10.1039/c1cc15995j))

Mak, Jeffrey Y. W. and Williams, Craig M. (2012). Erratum: Enantioselective total synthesis of ()-neovibsanin G and ()-14-epi-neovibsanin G (Chemical Communications (2012) (287-289) DOI: 10.1039/c1cc15995j)). Chemical Communications, 48 (100) doi: 10.1039/c2cc90426h

Erratum: Enantioselective total synthesis of ()-neovibsanin G and ()-14-epi-neovibsanin G (Chemical Communications (2012) (287-289) DOI: 10.1039/c1cc15995j))

2012

Journal Article

A combined DFT and NMR investigation of the zinc organometallic intermediate proposed in the syn-selective tandem chain extension-aldol reaction of β-keto esters

Aiken, Karelle S., Eger, Wilhelm A., Williams, Craig M., Spencer, Carley M. and Zercher, Charles K. (2012). A combined DFT and NMR investigation of the zinc organometallic intermediate proposed in the syn-selective tandem chain extension-aldol reaction of β-keto esters. Journal of Organic Chemistry, 77 (14), 5942-5955. doi: 10.1021/jo3004925

A combined DFT and NMR investigation of the zinc organometallic intermediate proposed in the syn-selective tandem chain extension-aldol reaction of β-keto esters

2012

Journal Article

Method in the madness - Methodology from total synthesis

Pouwer, Rebecca H. and Williams, Craig M. (2012). Method in the madness - Methodology from total synthesis. Synlett, 23 (10) ST-2011-A0782-A, 1446-1458. doi: 10.1055/s-0031-1290967

Method in the madness - Methodology from total synthesis

2012

Journal Article

Reductive Radical Decarboxylation of Aliphatic Carboxylic Acids

Ko, Eun Jung, Williams, Craig M., Savage, G. Paul and Tsanaktsidis, John (2012). Reductive Radical Decarboxylation of Aliphatic Carboxylic Acids. Organic Syntheses, 89, 471-479. doi: 10.15227/orgsyn.089.0471

Reductive Radical Decarboxylation of Aliphatic Carboxylic Acids

2012

Journal Article

Key achievements in the total synthesis of vibsane-type diterpenoids

Mak, Jeffrey Y. W. and Williams, Craig M. (2012). Key achievements in the total synthesis of vibsane-type diterpenoids. Natural Product Reports, 29 (4), 440-448. doi: 10.1039/c2np00067a

Key achievements in the total synthesis of vibsane-type diterpenoids

2012

Journal Article

Total synthesis of (-)-neovibsanin G and (-)-14-epi-neovibsanin G: Towards the synthesis of 15-O-methylneovibsanin F and 14-epi-15-O-methylneovibsanin F

Mak, Jeffrey Y. W. and Williams, Craig M. (2012). Total synthesis of (-)-neovibsanin G and (-)-14-epi-neovibsanin G: Towards the synthesis of 15-O-methylneovibsanin F and 14-epi-15-O-methylneovibsanin F. European Journal of Organic Chemistry, 2012 (10), 2001-2012. doi: 10.1002/ejoc.201101796

Total synthesis of (-)-neovibsanin G and (-)-14-epi-neovibsanin G: Towards the synthesis of 15-O-methylneovibsanin F and 14-epi-15-O-methylneovibsanin F

2012

Journal Article

Stereocontrolled Synthesis of the cis-Hydroxydecalin System: Towards Biologically Active 19-nor-Clerodanes

Mirzayans, Paul Malek, Pouwer, Rebecca H., Williams, Craig M. and Bernhardt, Paul V. (2012). Stereocontrolled Synthesis of the cis-Hydroxydecalin System: Towards Biologically Active 19-nor-Clerodanes. European Journal of Organic Chemistry, 8 (8), 1633-1638. doi: 10.1002/ejoc.201101807

Stereocontrolled Synthesis of the cis-Hydroxydecalin System: Towards Biologically Active 19-nor-Clerodanes

2012

Journal Article

2nd international collaborative and cooperative chemistry symposium

Williams, Craig (2012). 2nd international collaborative and cooperative chemistry symposium. Australian Journal of Chemistry, 65 (9), 1260-1261. doi: 10.1071/CH12231

2nd international collaborative and cooperative chemistry symposium

2012

Journal Article

Enantioselective total synthesis of the mexicanolides: khayasin, proceranolide, and mexicanolide

Faber, Jonathan M., Eger, Wilhelm A. and Williams, Craig M. (2012). Enantioselective total synthesis of the mexicanolides: khayasin, proceranolide, and mexicanolide. Journal of Organic Chemistry, 77 (20), 8913-8921. doi: 10.1021/jo301182f

Enantioselective total synthesis of the mexicanolides: khayasin, proceranolide, and mexicanolide

2012

Journal Article

Enantioselective total synthesis of (-)-neovibsanin G and (-)-14-epi-neovibsanin G

Mak, Jeffrey Y.W. and Williams, Craig M. (2012). Enantioselective total synthesis of (-)-neovibsanin G and (-)-14-epi-neovibsanin G. Chemical Communications, 48 (2), 287-289. doi: 10.1039/c1cc15995j

Enantioselective total synthesis of (-)-neovibsanin G and (-)-14-epi-neovibsanin G

2011

Journal Article

Synthesis of phenanthridine derivatives via photolysis

Linsenmeier, Anna M., Williams, Craig M. and Brase, Stefan (2011). Synthesis of phenanthridine derivatives via photolysis. Journal of Organic Chemistry, 76 (21), 9127-9132. doi: 10.1021/jo201542x

Synthesis of phenanthridine derivatives via photolysis

2011

Journal Article

Determining a synthetic approach to pierisformaside C

Chow, Sharon, Kress, Christoph, Albaek, Nanna, Jessen, Carsten and Williams, Craig M. (2011). Determining a synthetic approach to pierisformaside C. Organic Letters, 13 (19), 5286-5289. doi: 10.1021/ol202147r

Determining a synthetic approach to pierisformaside C

2011

Journal Article

The clerodane ring system: investigating the viability of a direct Diels-Alder approach

Merritt, Andrew T., Pouwer, Rebecca H., Williams, David J., Williams, Craig M. and Ley, Steven V. (2011). The clerodane ring system: investigating the viability of a direct Diels-Alder approach. Organic and Biomolecular Chemistry, 9 (13), 4745-4747. doi: 10.1039/c1ob05422h

The clerodane ring system: investigating the viability of a direct Diels-Alder approach

2011

Journal Article

ChemInform Abstract: Reducing the Cost, Smell, and Toxicity of the Barton Reductive Decarboxylation: Chloroform as the Hydrogen Atom Source.

Ko, Eun Jung, Savage, G. Paul, Williams, Craig M. and Tsanaktsidis, John (2011). ChemInform Abstract: Reducing the Cost, Smell, and Toxicity of the Barton Reductive Decarboxylation: Chloroform as the Hydrogen Atom Source.. ChemInform, 42 (30). doi: 10.1002/chin.201130044

ChemInform Abstract: Reducing the Cost, Smell, and Toxicity of the Barton Reductive Decarboxylation: Chloroform as the Hydrogen Atom Source.

2011

Journal Article

Understanding the reactivity of acyl anion equivalents: The epoxide ring opening case

Eger, Wilhelm A., Grange, Rebecca L, Schill, Heiko, Goumont, Régis, Clark, Timothy and Williams, Craig M. (2011). Understanding the reactivity of acyl anion equivalents: The epoxide ring opening case. European Journal of Organic Chemistry, 2011 (13), 2548-2553. doi: 10.1002/ejoc.201001680

Understanding the reactivity of acyl anion equivalents: The epoxide ring opening case

2011

Journal Article

Reducing the cost, smell, and toxicity of the Barton reductive decarboxylation: Chloroform as the hydrogen atom source

Ko, Eun Jung, Savage, G. Paul, Williams, Craig M. and Tsanaktsidis, John (2011). Reducing the cost, smell, and toxicity of the Barton reductive decarboxylation: Chloroform as the hydrogen atom source. Organic Letters, 13 (8), 1944-1947. doi: 10.1021/ol200290m

Reducing the cost, smell, and toxicity of the Barton reductive decarboxylation: Chloroform as the hydrogen atom source

2011

Journal Article

Isolation and confirmation of the proposed cleistanthol biogentic link from Croton insularis

Maslovskaya, LA, Savchenko, AI, Gordon, VA, Reddell, PW, Pierce, CJ, Parsons, PG and Williams, CM (2011). Isolation and confirmation of the proposed cleistanthol biogentic link from Croton insularis. Organic Letters, 13 (5), 1032-1035. doi: 10.1021/ol103083m

Isolation and confirmation of the proposed cleistanthol biogentic link from Croton insularis

2011

Journal Article

1,2,4-triazine vs. 1,3- and 1,4-oxazinones in normal- and inverse-electron-demand hetero-diels-alder reactions: Establishing a status quo by computational analysis

Rooshenas, Parham, Hof, Kira, Schreiner, Peter R. and Williams, Craig M. (2011). 1,2,4-triazine vs. 1,3- and 1,4-oxazinones in normal- and inverse-electron-demand hetero-diels-alder reactions: Establishing a status quo by computational analysis. European Journal of Organic Chemistry, 2011 (5), 983-992. doi: 10.1002/ejoc.201001365

1,2,4-triazine vs. 1,3- and 1,4-oxazinones in normal- and inverse-electron-demand hetero-diels-alder reactions: Establishing a status quo by computational analysis

2011

Journal Article

A concise total synthesis of (+/-)-cipadonoid B from synthetic azedaralide

Faber, Jonathan M. and Williams, Craig M. (2011). A concise total synthesis of (+/-)-cipadonoid B from synthetic azedaralide. Chemical Communications, 47 (8), 2258-2260. doi: 10.1039/c0cc04698a

A concise total synthesis of (+/-)-cipadonoid B from synthetic azedaralide

2011

Journal Article

Copper(I)-catalyzed cycloaddition of silver acetylides and azides: Incorporation of volatile acetylenes into the triazole core

Silvestri, Ilaria Proietti, Andemarian, Fikre, Khairallah, George N., Yap, Su Wan, Quach, Tim, Tsegay, Sammi, Williams, Craig M., O'Hair, Richard A. J., Donnelly, Paul S. and Williams, Spencer J. (2011). Copper(I)-catalyzed cycloaddition of silver acetylides and azides: Incorporation of volatile acetylenes into the triazole core. Organic and Biomolecular Chemistry, 9 (17), 6082-6088. doi: 10.1039/c1ob05360d

Copper(I)-catalyzed cycloaddition of silver acetylides and azides: Incorporation of volatile acetylenes into the triazole core