手性 (Chinese Wikipedia)

Analysis of information sources in references of the Wikipedia article "手性" in Chinese language version.

refsWebsite

Global rank Chinese rank

8doi.org

2^nd place

23^rd place

5nih.gov

4^th place

5^th place

2semanticscholar.org

11^th place

332^nd place

1acs.org

1,248^th place

434^th place

1worldcat.org

5^th place

12^th place

1archive.org

6^th place

4^th place

1sogou.com

low place

1,650^th place

1web.archive.org

1^st place

acs.org (Global: 1,248^th place; Chinese: 434^th place)

pubs.acs.org

Mislow, Kurt; Siegel, Jay. Stereoisomerism and local chirality. Journal of the American Chemical Society. May 1984, 106 (11): 3319–3328. ISSN 0002-7863. doi:10.1021/ja00323a043 （英语）.

archive.org (Global: 6^th place; Chinese: 4^th place)

JAFFE, IA; ALTMAN, K; MERRYMAN, P. The Antipyridoxine Effect of Penicillamine in Man.. The Journal of Clinical Investigation. Oct 1964, 43 (10): 1869–73. PMC 289631 . PMID 14236210. doi:10.1172/JCI105060.

doi.org (Global: 2^nd place; Chinese: 23^rd place)

^ Streitwieser, A., Jr.; Wolfe, J. R., Jr.; Schaeffer, W. D. Stereochemistry of the Primary Carbon. X. Stereochemical Configurations of Some Optically Active Deuterium Compounds. Tetrahedron. 1959, 6 (4): 338–344. doi:10.1016/0040-4020(59)80014-4.
Mislow, Kurt; Siegel, Jay. Stereoisomerism and local chirality. Journal of the American Chemical Society. May 1984, 106 (11): 3319–3328. ISSN 0002-7863. doi:10.1021/ja00323a043 （英语）.
Stephens, P. J.; Devlin, F. J.; Cheeseman, J. R.; Frisch, M. J.; Bortolini, O.; Besse, P. Determination of absolute configuration using calculation of optical rotation. Chirality. 2003, 15: S57–64. PMID 12884375. doi:10.1002/chir.10270.
Gal, Joseph. The Discovery of Stereoselectivity at Biological Receptors: Arnaldo Piutti and the Taste of the Asparagine Enantiomers-History and Analysis on the 125th Anniversary. Chirality. 2012, 24 (12): 959–976. PMID 23034823. doi:10.1002/chir.22071.
Theodore J. Leitereg; Dante G. Guadagni; Jean Harris; Thomas R. Mon; Roy Teranishi. Chemical and sensory data supporting the difference between the odors of the enantiomeric carvones. J. Agric. Food Chem. 1971, 19 (4): 785–787. doi:10.1021/jf60176a035.
Lepola U, Wade A, Andersen HF. Do equivalent doses of escitalopram and citalopram have similar efficacy? A pooled analysis of two positive placebo-controlled studies in major depressive disorder. Int Clin Psychopharmacol. May 2004, 19 (3): 149–55. PMID 15107657. S2CID 36768144. doi:10.1097/00004850-200405000-00005.
Hyttel, J.; Bøgesø, K. P.; Perregaard, J.; Sánchez, C. The pharmacological effect of citalopram resides in the (S)-(+)-enantiomer. Journal of Neural Transmission. 1992, 88 (2): 157–160. PMID 1632943. S2CID 20110906. doi:10.1007/BF01244820.
JAFFE, IA; ALTMAN, K; MERRYMAN, P. The Antipyridoxine Effect of Penicillamine in Man.. The Journal of Clinical Investigation. Oct 1964, 43 (10): 1869–73. PMC 289631 . PMID 14236210. doi:10.1172/JCI105060.

nih.gov (Global: 4^th place; Chinese: 5^th place)

ncbi.nlm.nih.gov

Stephens, P. J.; Devlin, F. J.; Cheeseman, J. R.; Frisch, M. J.; Bortolini, O.; Besse, P. Determination of absolute configuration using calculation of optical rotation. Chirality. 2003, 15: S57–64. PMID 12884375. doi:10.1002/chir.10270.
Gal, Joseph. The Discovery of Stereoselectivity at Biological Receptors: Arnaldo Piutti and the Taste of the Asparagine Enantiomers-History and Analysis on the 125th Anniversary. Chirality. 2012, 24 (12): 959–976. PMID 23034823. doi:10.1002/chir.22071.
Lepola U, Wade A, Andersen HF. Do equivalent doses of escitalopram and citalopram have similar efficacy? A pooled analysis of two positive placebo-controlled studies in major depressive disorder. Int Clin Psychopharmacol. May 2004, 19 (3): 149–55. PMID 15107657. S2CID 36768144. doi:10.1097/00004850-200405000-00005.
Hyttel, J.; Bøgesø, K. P.; Perregaard, J.; Sánchez, C. The pharmacological effect of citalopram resides in the (S)-(+)-enantiomer. Journal of Neural Transmission. 1992, 88 (2): 157–160. PMID 1632943. S2CID 20110906. doi:10.1007/BF01244820.
JAFFE, IA; ALTMAN, K; MERRYMAN, P. The Antipyridoxine Effect of Penicillamine in Man.. The Journal of Clinical Investigation. Oct 1964, 43 (10): 1869–73. PMC 289631 . PMID 14236210. doi:10.1172/JCI105060.

semanticscholar.org (Global: 11^th place; Chinese: 332^nd place)

api.semanticscholar.org

Lepola U, Wade A, Andersen HF. Do equivalent doses of escitalopram and citalopram have similar efficacy? A pooled analysis of two positive placebo-controlled studies in major depressive disorder. Int Clin Psychopharmacol. May 2004, 19 (3): 149–55. PMID 15107657. S2CID 36768144. doi:10.1097/00004850-200405000-00005.
Hyttel, J.; Bøgesø, K. P.; Perregaard, J.; Sánchez, C. The pharmacological effect of citalopram resides in the (S)-(+)-enantiomer. Journal of Neural Transmission. 1992, 88 (2): 157–160. PMID 1632943. S2CID 20110906. doi:10.1007/BF01244820.

sogou.com (Global: low place; Chinese: 1,650^th place)

readmodel.m.sogou.com

化学-选修三（人教版）p52. readmodel.m.sogou.com. [2020-07-08]. （原始内容存档于2020-07-10）.

web.archive.org (Global: 1^st place; Chinese: 1^st place)

化学-选修三（人教版）p52. readmodel.m.sogou.com. [2020-07-08]. （原始内容存档于2020-07-10）.

worldcat.org (Global: 5^th place; Chinese: 12^th place)

Mislow, Kurt; Siegel, Jay. Stereoisomerism and local chirality. Journal of the American Chemical Society. May 1984, 106 (11): 3319–3328. ISSN 0002-7863. doi:10.1021/ja00323a043 （英语）.

手性 (Chinese Wikipedia)

acs.org (Global: 1,248th place; Chinese: 434th place)

pubs.acs.org

archive.org (Global: 6th place; Chinese: 4th place)

doi.org (Global: 2nd place; Chinese: 23rd place)

nih.gov (Global: 4th place; Chinese: 5th place)