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Volumn 54, Issue 28, 2013, Pages 3617-3620

A pair of unprecedented spiro-trisindole enantiomers fused through a five-member ring from Laurencia similis

(9) Sun, Wen Shuang a Su, Shan a Zhu, Rong Xiu b Tu, Guang Zhong c Cheng, Wei a Liang, Hong a Guo, Xiao Yu a Zhao, Yu Ying a Zhang, Qing Ying a

a PEKING UNIVERSITY HEALTH SCIENCE CENTER (China)

b SHANDONG UNIVERSITY (China)

c BEIJING INSTITUTE OF MICROCHEMISTRY (China)

Author keywords

Laurencia similes; Similisine A; Similisine B; Spiro trisindole enantiomer

Indexed keywords

INDOLE ALKALOID; STAUROSPORINE;

ABSORPTION; ANTINEOPLASTIC ACTIVITY; ARTICLE; CANCER CELL CULTURE; CIRCULAR DICHROISM; DENSITY FUNCTIONAL THEORY; DRUG ISOLATION; DRUG STRUCTURE; DRUG SYNTHESIS; ENANTIOMER; HETERONUCLEAR MULTIPLE BOND CORRELATION; HETERONUCLEAR MULTIPLE QUANTUM COHERENCE; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HUMAN; HUMAN CELL; IC 50; LAURENCIA; LAURENCIA SIMILIS; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; OPTICAL ROTATION; RACEMIC MIXTURE; STEREOCHEMISTRY; ULTRAVIOLET SPECTROPHOTOMETRY;

LAURENCIA; LAURENCIA SIMILIS;

EID: 84878752557 PISSN: 00404039 EISSN: 18733581 Source Type: Journal
DOI: 10.1016/j.tetlet.2013.04.111 Document Type: Article

Times cited : (16)

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