Synthesis of brevetoxin sub-units by sequential ring-closing metathesis and hydroboration
- 1 January 1997
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 38 (1) , 123-126
- https://doi.org/10.1016/s0040-4039(96)02232-0
Abstract
No abstract availableKeywords
This publication has 32 references indexed in Scilit:
- A Series of Well‐Defined Metathesis Catalysts–Synthesis of [RuCl2(CHR′)(PR3)2] and Its ReactionsAngewandte Chemie International Edition in English, 1995
- Catalytic Ring‐Closing Metathesis: A New, Powerful Technique for Carbon–Carbon Coupling in Organic SynthesisAngewandte Chemie International Edition in English, 1995
- Efficient Synthesis of the Ring System in Hemibrevetoxin-B via Lactone Enol Triflate MethodSynlett, 1995
- The Synthesis of Cyclic Enol Ethers via Molybdenum Alkylidene-Catalyzed Ring-Closing MetathesisThe Journal of Organic Chemistry, 1994
- Synthesis of cycloalkenes via alkylidene-mediated olefin metathesis and carbonyl olefinationJournal of the American Chemical Society, 1993
- Bridging of macrodithionolactones to bicyclic systems. Synthesis and modeling of oxapolycyclic frameworksJournal of the American Chemical Society, 1990
- New synthetic strategies for the construction of medium size cyclic ethers. Stereocontrolled synthesis of the BCD ring framework of brevetoxin AJournal of the American Chemical Society, 1990
- Activation of 6-endo over 5-exo hydroxy epoxide openings. Stereoselective and ring selective synthesis of tetrahydrofuran and tetrahydropyran systemsJournal of the American Chemical Society, 1989
- Synthetic studies on the dioxepane region of brevetoxin B. New synthetic technology for the construction of oxepanes and synthesis of a model for the CDEF ring skeleton of brevetoxin BJournal of the American Chemical Society, 1989
- Transfer Reactions Involving Boron. V. Reactions of the Intermediate Organoboranes Formed by Hydroboration of Enol EthersJournal of the American Chemical Society, 1964