Albert W. M. Lee

Find an error

Name:
Organization: Hong Kong Baptist University , HongKong
Department: Department of Chemistry
Title: Professor(PhD)

TOPICS

Co-reporter:Albert W. M. Lee, Joseph K. Y. Ng, Eva Y. W. Wong, Alfred Tan, April K. Y. Lau, and Stephen F. Y. Lai
Journal of Chemical Education 2013 Volume 90(Issue 3) pp:388-389
Publication Date(Web):February 26, 2013
DOI:10.1021/ed200562f
Every student has a powerful wireless signal transmitter, his or her cell phone, that can be used to replace the “clicker” as a personal response device. Our mobile phone-based response system (iQlickers) collects and analyzes the answers or opinions sent in by the students as SMS (short message service) messages. The statistic of the answers is displayed online in the lecture hall. On the basis of the statistic, group discussion and peer instruction can be conducted. No setup in the lecture halls and purpose-built response pads (clickers) or receivers are needed. The operation cost of our system is very low, but class interaction can be greatly enhanced.Keywords: Distance Learning/Self Instruction; First-Year Undergraduate/General; Inquiry-Based/Discovery Learning; Organic Chemistry; Physical Chemistry; Problem Solving//Decision Making; Second-Year Undergraduate; Student-Centered Learning; Testing/Assessment;
Co-reporter:Ling-Yan Chen, Hao He, Wing-Hong Chan, and Albert W. M. Lee
The Journal of Organic Chemistry 2011 Volume 76(Issue 17) pp:7141-7147
Publication Date(Web):July 29, 2011
DOI:10.1021/jo2011335
Binaphthyl-based chiral sulfonimide (CSI) is demonstrated for the first time to be an efficient, strong Brønsted acid in asymmetric organocatalysis. A series of CSIs were synthesized and screened in the asymmetric Friedel–Crafts alkylation of indoles with imines. Good to excellent yields and enantioselectivities have been achieved. It was proved that it was crucial to wash the CSI catalyst with HCl before use.
Co-reporter:Qinghua Li;Wai-Yeung Wong;Wing-Hong Chan
Advanced Synthesis & Catalysis 2010 Volume 352( Issue 13) pp:2142-2146
Publication Date(Web):
DOI:10.1002/adsc.201000438

Abstract

In one step, the well known chiral auxiliary, Oppolzer’s camphor sultam, is turned into the new generation camphor sulfonyl hydrazine (CaSH II) organocatalyst. With the primary hydrazine functionality external to the tricyclic structure, CaSH II is active towards ketone substrates in asymmetric Diels–Alder reactions. The iminium intermediate of the catalytic cycle was isolated. When it was put back into the solution reaction system, the same level of yield and stereoselectivity was observed. Based on these observations, we argue that organocatlyst is actually an in situ chiral auxiliary.

Co-reporter:Hao He;Ling-Yan Chen;Wai-Yeung Wong;Wing-Hong Chan
European Journal of Organic Chemistry 2010 Volume 2010( Issue 22) pp:4181-4184
Publication Date(Web):
DOI:10.1002/ejoc.201000477

Abstract

A general approach to the synthesis of optically pure 3,3′-diaryl chiral sulfonimides (CSIs) from racemic BINOL has been developed. ortho-Lithiation is directed by the sulfonyl groups, and the resulting dihalides serve as the common precursors for the aryl-substituted CSIs.

Co-reporter:Bao-Jian Pei, Albert W.M. Lee
Tetrahedron Letters 2010 Volume 51(Issue 34) pp:4519-4522
Publication Date(Web):25 August 2010
DOI:10.1016/j.tetlet.2010.06.097
Co-reporter:Bao-Jian Pei, Wing-Hong Chan, and Albert W. M. Lee
The Journal of Organic Chemistry 2010 Volume 75(Issue 21) pp:7332-7337
Publication Date(Web):October 14, 2010
DOI:10.1021/jo1016025
With benzobisoxadisilole 1 as a 1,4-benzdiyne equivalent, oxadisilole fused triptycene 5 and extended triptycene 6 were synthesized. Triptycenes 5 and 6 are new precursors of triptycyne 7 and extended triptycyne 8 respectively via the phenyliodination/fluoride induced elimination protocol. Using these two arynes, a series of triptycene derivatives were synthesized.
Co-reporter:Hao He, Bao-Jian Pei and Albert W. M. Lee  
Green Chemistry 2009 vol. 11(Issue 11) pp:1857-1861
Publication Date(Web):07 Sep 2009
DOI:10.1039/B916265H
Oxidation of alkyl substituted aromatic compounds to ketones and carboxylic acids can be achieved by 70% aqueous TBHP (tert-butyl hydroperoxide) under microwave irradiation with no additional organic solvent, metal based reagent or catalyst. Methyl aromatics (toluenes and xylenes) can be oxidized directly to the industrially important benzoic and phthalic acids. An addition of a tiny amount of ionic liquid and simultaneous cooling improves the efficiency of these oxidations. For other alkyl substituted aromatics, ketones are obtained in good yields.
Co-reporter:Haiyan Wang, Albert W.M. Lee, Shaomin Shuang, Martin M.F. Choi
Microchemical Journal 2008 Volume 89(Issue 2) pp:90-97
Publication Date(Web):August 2008
DOI:10.1016/j.microc.2007.12.006
A fast and cost-effective method using HPLC/UV has been developed for determination of acrylamide in deep-fried flour-based leaven dough foods available in Hong Kong. The samples were purified by a simple solid-phase extraction method which combined Oasis HLB and Bond Elut-Accucat cartridges. The aqueous sample solution was centrifuged at 14,500 ×g and 0 °C for 15 min to successfully remove the fat in the samples. A gradient elution program and a mobile phase of 4.0% v/v acetonitrile in water allowed sufficient retention and well resolved acrylamide from the food matrices in the sample extracts. Acrylamide was detected at UV wavelengths of 210 and 225 nm. The amounts of acrylamide in eight food samples were 27–198 μg/kg when 1-g samples were analyzed. The recoveries of acrylamide were larger than 78.0% and the precisions were 2.1–10.9% (n = 3). Our proposed method is especially relevant for analyzing acrylamide in those oily food matrices.
Co-reporter:Albert W. M. Lee, Anissa B. W. Yeung, Mabel S. M. Yuen, H. Zhang, X. Zhao and W. Y. Wong  
Chemical Communications 2000 (Issue 1) pp:75-76
Publication Date(Web):07 Jan 2000
DOI:10.1039/A908220D
Linear acetylenic and diacetylenic sulfides consisting of up to eight triple-bond units with alternating sulfur atoms and acetylene units were synthesized.
Bicyclo[2.2.1]hept-5-ene-2-carboxaldehyde, 3-propyl-, (1R,2R,3R,4S)-
Benzene, 1-[(R)-ethynylsulfinyl]-4-methyl-
Heptacyclo[31.3.1.13,7.19,13.115,19.121,25.127,31]dotetraconta-1(37),3,5,7(42),9,11,13(41),15,17,19(40),21,23,25(39),27,29,31(38),33,35-octadecaene
Naphthaceno[2,3-c][1,2,5]oxadisilole, 1,3-dihydro-1,1,3,3-tetramethyl-
Anthra[2,3-c][1,2,5]oxadisilole, 1,3-dihydro-1,1,3,3-tetramethyl-
Benzonitrile, 3-chloro-2,6-dimethoxy-, N-oxide
1,4-Butanediol, 2-(phenylmethyl)-, (2R)-
Isothiazole, 2,3-dihydro-2-[(1S)-1-(1-naphthalenyl)ethyl]-, 1,1-dioxide
1,3-Benzenedicarboxaldehyde, 2-hydroxy-5-methoxy-
Silane, (thiodi-2,1-ethynediyl)bis[trimethyl-