First total synthesis of (±)-floribundane B: An approach based on Johnson-Claisen rearrangement of a Morita-Baylis-Hillman adduct
暂无分享,去创建一个
[1] Wender A. Silva,et al. Unprecedented E-stereoselectivity on the sigmatropic Hurd-Claisen rearrangement of Morita-Baylis-Hillman adducts: a joint experimental-theoretical study. , 2019, Organic & biomolecular chemistry.
[2] Wender A. Silva,et al. Recent Advances in the Asymmetric Claisen Rearrangement Promoted by Chiral Organometallic Lewis Acids or Organic Bronsted-Lowry Acids , 2015 .
[3] C. Hertweck,et al. Twofold polyketide branching by a stereoselective enzymatic Michael addition. , 2015, Chemical communications.
[4] G. Zanoni,et al. A Concise and Efficient Total Synthesis of Oleocanthal , 2013 .
[5] J. Rehbein,et al. Claisen Rearrangement of Aliphatic Allyl Vinyl Ethers from 1912 to 2012: 100 Years of Electrophilic Catalysis , 2013 .
[6] H. Morita,et al. Formal synthesis of (−)-oleocanthal by means of a SmI2-promoted intramolecular coupling of bromoalkyne with α,β-unsaturated ester , 2012 .
[7] D. Mendonça,et al. Iridoids from Hymenodictyon floribundum , 2010 .
[8] Robert M. Williams,et al. Synthesis of (+/-)-Oleocanthal via a Tandem Intramolecular Michael Cyclization-HWE Olefination. , 2009, Tetrahedron letters.
[9] M. Brimble,et al. Synthetic Studies Towards the Anti-inflammatory Agent, Oleocanthal using a Johnson-Claisen (Orthoester) Rearrangement Strategy , 2009 .
[10] Jeffrey B. Sperry,et al. Syntheses of (-)-oleocanthal, a natural NSAID found in extra virgin olive oil, the (-)-deacetoxy-oleuropein aglycone, and related analogues. , 2007, The Journal of organic chemistry.
[11] Andrea D'Annibale,et al. Synthesis of alkyl-substituted six-membered lactones through ring-closing metathesis of homoallyl acrylates. An easy route to pyran-2-ones, constituents of tobacco flavor. , 2007, The Journal of organic chemistry.
[12] B. Das,et al. I2–SiO2: An efficient heterogeneous catalyst for the Johnson–Claisen rearrangement of Baylis–Hillman adducts ☆ , 2007 .
[13] G. Beauchamp,et al. Synthesis and assignment of absolute configuration of (-)-oleocanthal: a potent, naturally occurring non-steroidal anti-inflammatory and anti-oxidant agent derived from extra virgin olive oils. , 2005, Organic letters.
[14] R. Keast,et al. Phytochemistry: Ibuprofen-like activity in extra-virgin olive oil , 2005, Nature.
[15] J. Jauch. A new protocol for Baylis-Hillman reactions: chirality transfer in a lithium phenylselenide induced tandem-michael-aldol-retro-michael reaction. , 2001, The Journal of organic chemistry.
[16] J. Ardisson,et al. Approach Towards the Total Synthesis of Rhizoxin: Enantioselective Preparation of the Lactone Core , 2001 .
[17] D. Basavaiah,et al. Unprecedented stereochemical reversal from alkyl to aryl substituents in the Johnson-Claisen rearrangement of methyl 3-hydroxy-2-methylenealkanoates , 1996 .
[18] S. Chandrasekaran,et al. A general approach to the synthesis of 5,6-dihydro-2(2H)pyranones; simple synthesis of α-pyrone, (±)-argentilactone and (±)-goniothalamin , 1989 .
[19] F. Bonadies,et al. Use of pyridinium chlorochromate as methylene oxidant in 5,6-dihydropyrans: a practical one-step preparation of the anhydromevalonolactone , 1984 .
[20] Y. Ban,et al. SYNTHESIS OF 5,6-DIHYDRO-2-PYRONE AND 2-PYRONE , 1974 .
[21] P. A. Meulman,et al. PREPARATION OF CALCIUM ELENOLATE FROM OLIVE PRESS JUICE , 1972 .