Professor Gon-Ann Lee
Phone |
(O) (02)2905-3563 (LAB)(02)29053582 |
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Experiences and honors: |
B.S., the M.S., the Ph.D., the |
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Postdoctoral
Research, the Associate
Professor, Professor, Chairman, Department of Chemistry, Fu-Jen Cathholic University (1999-2002)(2009-2012) |
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Field |
Organic Chemistry |
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Research Interests |
Dr. Lee's research interests include the synthesis of high strain of small ring compounds (cyclopropenes), calix[4]arenes, and the chemistry of metal-cyclopropenes. A major focus of his research has been the development of a vacuum gas-solid reaction (VGSR) technique for the synthesis of small ring cycloalkenes using reagents adsorbed on inert surfaces to effect elimination reactions. This approach allows the reactive species to be isolated at low temperature, and eliminates many of the undesired bimolecular side reactions that would normally be encountered in solution. Energetic compounds can thus be collected readily in cold traps for further chemical studies or spectral characterization. |
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Recent Publications |
1-
Lee, G.-A.,* Lin, H.-C., Lee, H.-Y., Chen, C.-H., Huang, H.-Y., “Ipso Nitration
of 2-Halothiophenes with Silver Nitrate, ” Asian J. Org. Chem. 2017,
6, 1733-1736. 2-
Lee, G.-A.,* Shih, Y.-F., Lin,
H.-C., Wang, W.-C., Chan, H.-T., Lee, H.-Y., Lee, C.-Y., “Synthesis of Calix[6]thiophenes and Calix[6]furans, ” ChemistrySelect 2020, 5, 8518-8521. 3-
Lin, H.-C., Tsai, R.-T., Wu,
H.-P., Lee, H.-Y., Lee, G.-A.,* “Ene di- and trimerization of 1-methyl-2-cyclopropene, ” Tetrahedron, 2016, 72, 184-191. 4-
Lin, C.-N., Huang, C.-Y., Yu, C.-C., Chen,
Y.-M., Ke, W.-M.,Wang, G.-J., Lee, G.-A.,* Shieh, M.-H.,* “Iron carbonyl cluster-incorporated Cu(I)
NHC complexes in homocoupling of arylboronic acids: an effective [TeFe3(CO)9]2-ligand, ” Dalton
Transactions, 2015, 44,
16675-16679. 5-
Lee, G.-A.,* Lee, H.-Y., Chen, W.-C., Lin, Y.-H., “Reaction of,-unsaturated N-benzenesulfonyl Imine – N –
[(2E)-3-phenyl-2-propen-1-ylidene] benzenesulfonamide
with Methyllithium, ” J. Chin.
Chem. Soc. 2015, 62,
573-576. 6-
Lee, G.-A.,* Lin, H.-C., “Synthesis of an Anti-Bredt
Compound, Bicyclo[3.2.2]nona-1,6,8-triene, via the Isomerization of
Tricyclo[3.2.1.02,4]nona-2,6-diene, ”
Org. Lett. 2014, 16, 5275−5277. 7-
Lee, G.-A.,* Lee, H.-Y., Wang,
W.-C., Cherng, C.-H., “Auto de-bromine-coupling reactions of
1-aryl-7-bromocycloheptenes,” Tetrahedron, 2014, 70, 2956-2961. 8-
Lee, G.-A.,* Chan, L.-E., Tsai, R.-T., Chang,
K.-C., “Generation and Chemistry of Tricyclo[3.2.1.02,4]oct-2(3)-ene,” Eur.
J. Org. Chem. 2012, 2824–2830. 9-
Lee, G.-A.,* Wang, W.-C., Shieh,
M., Kuo, T.-S., “A Novel Synthesis of Calix[4]thiophenes and
Calix[4]furans,” Chem. Commun. 2010, 46,
5009–5011. 10-
Lee, G.-A.,* Tsai, R.-T., Wang, W.-C., Liu, Y.-T., “The Synthesis and
Trapping of 1-Naphthylcyclopropenes,” J.
Chin. Chem. Soc. 2010, 57,
800-804. 11-
Lee, G.-A.,* Wang, W.-C., Jiang, S.-F., Chang, C.-Y., Tsai, R.-T., “The
Crossed [2+2] Cycloaddition of 1-Phenylcyclopropene and Bromo-2-phenylcyclopropene,” J.
Org. Chem. 2009, 74, 7994–7997. 12-
Lee,
G.-A.,* Chen, K.-C., “The
General Synthesis and Trapping of 3-Substituted 1-Chlorocyclopropenes,” Org. Lett. 2008, 9, 1843-1845. 13-
Lo, Y.-L., Wang, W.-C., Lee, G.-A.,
Liu, Y.-H.,* “Bis(u-l-1H-benzimidazole-5,6-dicarboxylato)bis[tetraaquadicobalt(II)] pentahydrate,” Acta Cryst. 2007, E63, m2657-m2658. 14-
Chen,
K.-C., Wang, W.-C., Chen, M.-Y., Chen, W.-C., Her, M.-C., Lee, G.-A.,*
“Regio- and Stereoselectivity of Ene Reactions: The
Dimerization of Bicyclic 1,3-Fused
2-(TrimethylSilyl)cycloprop-1-enes,” Eur. J. Org. Chem. 2007, 953-958. 15-
陳科州, 李國安,* “環丙烯類化合物的合成與化學性質,” Chemistry (J. Chin. Chem.
Soc., Taipei) 2006, 64, 73-96. 16-
Lai,
Y.-W., Cherng, J.-J., Sheu, W.-S., Lee, G.-A., Shieh,
M.,* “Novel Types of Organic S-Fe-CO Complexes: Reaction of [SFe3(CO)9]2- with Propargyl Bromide,” Organometallics. 2006, 25, 184-190. 17-
Lee, G.-A.,*
Chang, C.-Y., “Novel Ene Trimerization of
1-Phenylcyclopropene,” J. Org, Chem. 2004, 69, 8949-8951. 18-
Lee, G.-A.,* Chang, C.-Y., Cherng, C.-H., Chen, C.-S., Liu,
M., “The Synthesis and Chemistry of 1,3-Bridged Polycyclic Cyclopropenes: 8-Oxatricyclo[3.2.1.02,4]octa-2,6-dienes,” J.
Chin. Chem. Soc. 2004, 51, 839-845. 19-
Lee, G.-A.,* Cherng,
C.-H., Huang, A.-N., Lin, Y.-H., “Synthesis and Chemistry of
Tricyclic cyclopropene-tricyclo[3.2.2.02,4]nona-2(4),6-diene,” Tetrahedron. 2003, 59, 1539-1545. 20-
Lee,
G.-A.,* Lin,
Y.-H., Huang, A.-N., Li, Y.-C., Chen, C.-S., Jann, Y.-C., Chen, C.-S.,
“Isomerization of tricyclo[3.2.2.02,4]nona-2(4),6-diene to the Anti-Bredt Compound
8-Methylenebicyclo[3.2.1]octa-1,6-diene,” J. Am. Chem. Soc. 1999, 121, 5328-5329. 21-
Lee,
G.-A.,* Chen, P.-K., Chen,
M.-Y., “The Synthesis and Chemistry of
8-Substituted Bicyclo[5.1.0]oct-1(8)-ene ,” J. Chin. Chem.
Soc. 1998, 45, 381-385. 22-
Lee,
G.-A.,* Chang, C.-Y.,
“Novel Tetramerization of 1-Trimethylsilyl-2-Phenylcyclopropene,” Tetrahedron Lett. 1998, 39, 3013-3016. 23-
Lee,
G.-A.,* Chen, C.-S.,
“1-Chloro-3-trimethysilylcyclopropene -- A New Synthesis of
3,3'-Bicyclopropyl,” Tetrahedron Lett. 1997, 38, 8717-8720. 24-
Lee,
G.-A.,* Huang, A.-N., Chen,
C.-S., Li, Y.-C., Jann, Y.-C., “1,2-Bridged
Tricyclic Cyclopropenes:Tricyclo[3.2.1.02,4]octa-2(4),6-diene
and Tricyclo[3.2.1.02,4]oct-2(4)-ene,” J.
Org. Chem. 1997, 62, 3355-3359. 25-
Chou,
S.-S. P., Lee, G.-A.,* “Improvement of Chemistry Courses for
Non-Chemistry Major Undergraduates,” J. Chin. Chem.
Soc. 1996, 54, 131-143. 26-
Lee,
G.-A.,* Chen, J., Chen,
C.-S., Shiau, C.-H., Cherng C.-H., “The Synthesis and
Chemistry of 9-Chlorobicyclo[6.1.0]non-1(9)-ene,” J. Chin. Chem. Soc. 1996, 43, 297-300. 27-
, “Synthesis and chemistry
of Bicyclo[4.1.0]hept-1,6-ene ,” J. Org. Chem. 1996, 61, 764-770. 28-
Lee, G.-A.,* Shiau,
C.-S., Chen, C.-S., Chen, J., “Regioselectivity of the Ene Reaction:
Dimerization of 8-Chlorobicyclo[5.1.0]oct-1(8)-ene,” J. Org. Chem. 1995, 60, 3565-3567. 29- Billups, W.-E.,* Lee, G.-A., Arney, B.-E., Jr., Whitmire, K.-H., “1,3-Bridged Cyclopropenes,” J. Am. Chem. Soc. 1991, 113, 7980-7984. 30- Billups, W.-E.,* Haley, M.-M., Lee, G.-A., “Bicyclo[n.1.0]alkenes,” Chem. Rev. 1989, 89, 1147-1159. |