The total synthesis of eleutherobin: A surprise ending Journal Article
| Authors: | Chen, X. T.; Zhou, B.; Bhattacharya, S. K.; Gutteridge, C. E.; Pettus, T. R. R.; Danishefsky, S. J. |
| Article Title: | The total synthesis of eleutherobin: A surprise ending |
| Abstract: | An 'sp2-sp3 Stille coupling' of the vinyl triflate 1 and the stannyl compound 2 is a key step toward the completion of the total synthesis of eleutherobin, a natural product exhibiting taxol-like cytotoxic activity. |
| Keywords: | glycosylations; total synthesis; antitumor agents; eleutherobin; stille coupling |
| Journal Title: | Angewandte Chemie - International Edition |
| Volume: | 37 |
| Issue: | 6 |
| ISSN: | 1433-7851 |
| Publisher: | Wiley Blackwell |
| Date Published: | 1998-04-03 |
| Start Page: | 789 |
| End Page: | 792 |
| Language: | English |
| DOI: | 10.1002/(sici)1521-3773(19980403)37:6<789::aid-anie789>3.0.co;2-3 |
| PROVIDER: | scopus |
| DOI/URL: | |
| Notes: | Article -- Export Date: 12 December 2016 -- Source: Scopus |
