Total Synthesis of Tryprostatin B: Generation of a Nucleophilic Prenylating Species from a Prenylstannane
- 1 January 1996
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 118 (49) , 12463-12464
- https://doi.org/10.1021/ja962954o
Abstract
No abstract availableThis publication has 21 references indexed in Scilit:
- Staurosporine and ent-Staurosporine: The First Total Syntheses, Prospects for a Regioselective Approach, and Activity Profiles1Journal of the American Chemical Society, 1996
- Total Synthesis of GypsetinJournal of the American Chemical Society, 1995
- First Total Synthesis of Staurosporine and ent-StaurosporineJournal of the American Chemical Society, 1995
- Effective 1,5-Asymmetric Induction in Tin(IV) Chloride Promoted Reactions Between Aldehydes and (4-Alkoxy-2-alkenyl)tributylstannanesSynthesis, 1994
- Total synthesis of strychnan- and aspidospermatan-type alkaloids. 2. Generation of 15-(3-furanyl) ABCE tetracyclic intermediatesThe Journal of Organic Chemistry, 1993
- Studies on the synthesis of mavacurine-type indole alkaloids. First total synthesis of (±)-2,7-dihydropleiocarpamineThe Journal of Organic Chemistry, 1993
- The mechanism of tin tetrachloride promoted additions of allylstannanes to aldehydes: a response to Denmark, Wilson, and WillsonJournal of the American Chemical Society, 1989
- On the Lewis-acid-induced addition of allylstannanes to aldehydes: a spectroscopic investigationJournal of the American Chemical Society, 1988
- Regioreversed addition of but-2-enyltributylstannane to aldehydes in the presence of aluminium chloride–propan-2-olJournal of the Chemical Society, Chemical Communications, 1983
- Trimethylsilyl iodide as a peptide deblocking agentJournal of the Chemical Society, Chemical Communications, 1979