论文信息 - Studies toward the enantioselective synthesis of neurymenolide A: Construction of the macrocyclic core via Claisen rearrangement - 字舞流文

Studies toward the enantioselective synthesis of neurymenolide A: Construction of the macrocyclic core via Claisen rearrangement

Tsuneomi Kawasaki | S. Aiba | Hidenori Watanabe | M. Masuda | Yusuke Ogura | Natsuki Sakurai | H. Takikawa | N. Mori | Tetsuji Murase

[1] B. Baratte,et al. Neurymenolide A, a Novel Mitotic Spindle Poison from the New Caledonian Rhodophyta Phacelocarpus neurymenioides , 2019, Marine drugs.

[2] Thomas O. Ronson,et al. 4-Hydroxy-6-alkyl-2-pyrones as nucleophilic coupling partners in Mitsunobu reactions and oxa-Michael additions , 2014, Beilstein journal of organic chemistry.

[3] A. Fürstner,et al. Total synthesis of neurymenolide A based on a gold-catalyzed synthesis of 4-hydroxy-2-pyrones. , 2012, Angewandte Chemie.

[4] E. P. Stout,et al. Antibacterial neurymenolides from the Fijian red alga Neurymenia fraxinifolia. , 2009, Organic letters.

[5] R. Hsung,et al. Syntheses of 2-Pyrones via Electrophilic Substitutions at C7 of 4-Hydroxy-6-methyl-2-pyrone through Mono- or Dianion Formation , 2007 .

[6] D. A. Wacker,et al. Efficient solid-phase synthesis of 2,3-substituted indoles , 2002 .

[7] M. Moreno-Mañas,et al. Palladium-catalyzed C-alkylations of the highly acidic and enolic triacetic acid lactone. Mechanism and stereochemistry , 1988 .

[8] E. Corey,et al. Leukotriene B. Total synthesis and assignment of stereochemistry , 1980 .

[9] V. Paul,et al. New macrocyclic - and -pyrones from the marine red alga , 1986 .