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Saturday, 17 January 2015

Yu Luo

Yu Luo
Associate Professor

Department of Chemistry
Institute of Technology Department of Chemistry
Tel: 021-54345462
Office Location: Minhang Chemistry Building 535
E-mail: yluo@chem.ecnu.edu.cn
Mailing address: 500 Dongchuan Road, East China Normal University Minhang Campus Chemistry Building 535


1: [a]D20 10.0 (c, 0.20, EtOH); mp 76–77 deg C;

1H NMR (500 MHz, CDCl3): d1.15 (t, 3H, J = 7.5 Hz), 1.60 (m, 1H), 1.70 (m, 1H), 2.02 (m, 1H), 2.19 (q, 2H, J = 7.5 Hz), 2.32 (m, 1H), 2.76 (m, 1H), 2.85 (m, 1H), 3.11 (m,
1H), 3.41 (m, 2H), 3.79 (s, 3H), 5.48 (s, 1H), 6.71 (dd, 1H, J = 2.0 Hz, 8.5 Hz), 6.75 (s, 1H), 7.11 (d, 1H, J = 8.0 Hz).

13C NMR (100 MHz,DMSO–d6): d 173.7, 158.7, 148.1, 135.8, 124.9, 112.3, 109.2, 55.5, 42.7, 37.9, 34.8, 32.5, 30.6, 29.8, 9.9. EI-MS: 247 ([M]+); HR-MS 247.1572
([M]+, C15H21NO2; Calcd. 247.1571).

The enantiomeric excess of (S)-1 was determined by HPLC as >99.9% [column, CHIRALPAK AS-H
(4.6 mm 250 mm), room temperature; eluent, hexane-2-propanol-trifluoroacetic acid (90:10:0.1); flow rate, 1.0 mL/min; detect, 290 nm; tR
of (S)-1, 30.7 min; tR of (R)-1 (enantiomer of (S)-1), 37.1 min].

S.B. Yu et al. / Chinese Chemical Letters 22 (2011) 264–267
: wlu@chem.ecnu.edu.cn (W. Lu).
Synthesis of the key intermediate of ramelteon
Shan Bao Yu a, Hao Min Liu a, Yu Luo a, Wei Lu b,

*a Department of Chemistry, , Shanghai 200062, China

b Institute of Drug Discovery and Development, East China Normal University, Shanghai 200062, China



(1) small molecule medicinal chemistry research. Including anticancer drugs, anti-hepatitis drugs and hypoglycemic drug design, synthesis and pharmacological properties of
(2) study of drug synthesis and fine chemicals. Includes a plurality of anticancer drugs, vitamin D drugs, natural phospholipids, as well as new anti-HIV drugs condensing agent, amino acid synthesis Studies link like fine chemicals
(3) research initiative targeted drug delivery technology based on liposomes, microspheres, vesicles, etc.


Academic Achievements

Recently published research papers 
1. Chen, TJ; Luo Y*; Hu, YH; Yang, B; Lu W, European Journal of Medicinal Chemistry201364, 613-620
2. Zhang, X; Zhang, J; Tong, LJ; Luo, Y; Su, MB; Zhang, Y; Li, J; Lu, W*; Chen, Y*, Bioorganic & Medicinal Chemistry201321, 3240-3244.
3. Luo, P; Luo, Y; Huang, J; Lu, W; Luo, DJ; Yu, JH*, Liu, SY, Colloids and Surfaces B: Biointerfaces2013109, 167-175. 
4. Mei, TW; Luo, Y*, Feng, XJ; Lu, W*; Yang, B,  Tetrahedron201369, 2927 – 2932
5. Wu, QE; Du, F; Luo, Y; Lu, W; Huang, J; Yu, JH*; Liu, SY*, Colloids and Surfaces B: Biointerfaces2013105, 294-302. 
6. Yong, DW; Luo, Y; Du, F; Huang, J; Lu, W; Dai, ZY; Yu, JH*; Liu, SY*, 2013105, 31-36.
7. Chen, TJ; Huang, QQ; Luo, Y*, Hu, YH*, Lu, W, Tetrahedron Letters201354, 1401-1404.
8. Luo,Y; Yu, SB; T, LJ; H, QQ; Lu, W; Chen, Y. European Journal of Medicinal Chemistry201254, 281-286.
9. Feng, XJ; Mei YH; Luo, Y*; Lu W, Monatshefte fur Chemie - Chemical Monthly2012143 , 161-164
10. Yu, SB; Huang, QQ; Luo, Y*; Lu, W*, Journal of Organic Chemistry 201277, 713-717.
11. Song, Y; Yuan, W; Luo, Y*; Lu, W Chinese Chemical Letters 201223, 154-156.
12. Zhang, LJ; Luo, Y; Yu, SB; Lu, W*,  Journal of Heterocyclic Chemistry201249, 1254-1256
13. Luo, Y; Xiao, F; Qian, SJ; He, QJ; Lu, W*; Yang, B* Synthesis and Evaluation of Novel 5-a, ß-unsaturated sulfonyl-indolin-2-ones as Potent Cytotoxic Agents,MedChemCommun20112, 1054 - 1057
14. Luo, Y; Liu, HM; Su, MB; Sheng, L; Zhou, YB; Li, J*; Lu, W* Synthesis and Biological Evaluation of Piper Amide Analogues as HDAC Inhibitors, Bioorganic & Medicinal Chemistry Letters201121, 4844-4866
15. Zhang, LJ; Xia, WP; Wang, B; Luo, Y*; Lu, W*, Convenient Synthesis of Sorafenib and ItsDerivatives, Synthetic Communications201141, 3140-3146
16. Luo, Y; Xiao, F; Qian, SJ; Lu, W*, Yang, B, Synthesis and in vitro cytotoxic evaluation of some thiazolylbenzimidazole derivatives, European Journal of Medicinal Chemistry,201146, 417-422.
17. Luo, Y; Yao, JP; Yang, L; Feng, CL; Tang, W; Wang, GF; Zuo, JP*; Lu, W*, Synthesis and Anti-Hepatitis B Virus Activity of a Novel Class of Thiazolylbenzimidazole Derivatives, Arch. Pharm. Chem. Life Sci. 20112, 78–83
18. Yu, SB; Liu, HM; Luo, Y; Lu, W*, Synthesis of the key intermediate of ramelteon, Chinese Chemical Letters201122,264–267
19. Luo, Y; Yao, JP; Yang, L; Feng, CL; Tang, W; Wang, GF; Zuo, JP*; Lu, W*, Design and synthesis of novel benzimidazole derivatives as inhibitors, Bioorganic & Medicinal Chemistry201018, 5048-5055.
20. Liu, HY; Xia, WP; Luo, Y; Lu, W*, A novel synthesis of imatinib and its intermediates, Monatshefte fur Chemie - Chemical Monthly2010141, 907-911.
21. Yu, SB; Luo, Y; Liu, HY; Liu, HM; Lu, W*, Synthesis of the DE synthon of racemic camptothecin, Monatshefte fur Chemie - Chemical Monthly2010141, 245-249.
22. Wang, B; Zhang, LJ; Fu, KY; Luo, Y*; Lu, W; Tang, J, An Efficient Synthesis of 1,2,6,7-Tetrahydro-8H-indeno[5,4-b]furan-8-one, Organic Preparations and Procedures International200941, 309-314.

Granted patent
ZL201010137564.1; Synthesis method phosphatidylethanolamine
ZL200910049896.1; multi-substituted pyridone compound synthesis
ZL200910054400.X; key intermediate in the synthesis method for the preparation of camptothecin compounds
ZL200710066688.3; a water-soluble derivative of camptothecin and its preparation method and application
ZL200810034511.X; (2- cyano - isopropyl) - Preparation of 3,5-toluene
ZL200910114955.9; one kind morpholine-carboxylic acid amides of N, N- dimethyl-4- do
ZL200810042729.X; Synthesis of 1,2,6,7-tetrahydro -8H- indeno [5,4-b] furan-8-one Method

The research project
National Drug Discovery major projects a sub-topics,Shanghai Natural Science Foundation 1, the Ministry of Education funds a young teacher, the State Key Laboratory of Drug Research Fund 1, business cooperation projects 5

 September 2014 to celebrate the 15th anniversary of Professor Lv Wei from previous teaching students gathering
15th anniversary party


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