Regioselectivity of Pictet–Spengler cyclization reactions to construct the pentacyclic frameworks of the ecteinascidin–saframycin class of tetrahydroisoquinoline antitumor antibiotics
- 24 March 2007
- journal article
- research article
- Published by Elsevier in Tetrahedron Letters
- Vol. 48 (21) , 3719-3722
- https://doi.org/10.1016/j.tetlet.2007.03.113
Abstract
No abstract availableKeywords
This publication has 28 references indexed in Scilit:
- Asymmetric Total Synthesis of (−)‐Cribrostatin 4 (Renieramycin H)Angewandte Chemie International Edition in English, 2007
- Asymmetric Total Syntheses of Ecteinascidin 597 and Ecteinascidin 583Angewandte Chemie International Edition in English, 2006
- Stereospecific Formal Total Synthesis of Ecteinascidin 743Angewandte Chemie International Edition in English, 2006
- The Solution to a Deep Stereochemical Conundrum: Studies toward the Tetrahydroisoquinoline AlkaloidsAngewandte Chemie International Edition in English, 2006
- Total Synthesis of Ecteinascidin 743Journal of the American Chemical Society, 2005
- Synthetic Studies toward Ecteinascidin 743The Journal of Organic Chemistry, 2005
- A Practical Synthesis of the ABC Ring Model of Ecteinascidins.CHEMICAL & PHARMACEUTICAL BULLETIN, 2000
- Synthetic Study on Ecteinascidin 743 Starting from d-GlucoseSynlett, 1999
- An Improved Synthesis of the ABC Ring Model of EcteinascidinsHETEROCYCLES, 1999
- Enantioselective Total Synthesis of Ecteinascidin 743Journal of the American Chemical Society, 1996