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Cited by 35 publications
(25 citation statements)
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“…As a consequence, huge investments have been made to study the chemistry of natural products. Nowadays, the use of natural molecular fingerprints as a source of inspiration for the acquisition of new bioactive chemical entities has proven to be a very promising and efficient method (Newman et al, 2000;Hanessian, 2006;Baker et al, 2007).…”
Section: Research Articlementioning
confidence: 99%
“…As a consequence, huge investments have been made to study the chemistry of natural products. Nowadays, the use of natural molecular fingerprints as a source of inspiration for the acquisition of new bioactive chemical entities has proven to be a very promising and efficient method (Newman et al, 2000;Hanessian, 2006;Baker et al, 2007).…”
Section: Research Articlementioning
confidence: 99%
“…[ either reduction or oxidation gave the corresponding chiral pyrrolidine 11 a, acid 12 a, and diamine 12 aa. [1] The absolute stereochemistry of the highly substituted quaternary proline derivatives 8 was confirmed by the X-ray crystallographic analysis of 8 c (2S, 3R, 4R, 5S; Figure 2). [1] The absolute stereochemistry of the highly substituted quaternary proline derivatives 8 was confirmed by the X-ray crystallographic analysis of 8 c (2S, 3R, 4R, 5S; Figure 2).…”
Section: Yieldmentioning
confidence: 82%
“…It is hoped that an effective therapeutic agent will emerge in the near future. In this regard, fruitful collaborations between academia and pharmaceutical or biotech companies could continue to play an important role [22]. …”
Section: Synopsismentioning
confidence: 99%