Total Synthesis of Tetrahydropyran-Containing Natural Products Exploiting Intramolecular Oxa-Conjugate Cyclization

article by Haruhiko Fuwa published 2012 in Heterocycles

Total Synthesis of Tetrahydropyran-Containing Natural Products Exploiting Intramolecular Oxa-Conjugate Cyclization is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.3987/REV-12-730

P50authorHaruhiko FuwaQ39569291
P2860cites workHalichondrins - antitumor polyether macrolides from a marine spongeQ62773345
Structure Revision of Aspergillides A and B, Cytotoxic 14-Membered Macrolides fromAspergillus ostianus, by X-ray CrystallographyQ104971935
P433issue6
P921main subjectnatural productQ901227
P304page(s)1255
P577publication date2012-01-01
P1433published inHeterocyclesQ898691
P1476titleTotal Synthesis of Tetrahydropyran-Containing Natural Products Exploiting Intramolecular Oxa-Conjugate Cyclization
P478volume85

Reverse relations

cites work (P2860)
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Q42205765Catalyst-directed diastereo- and site-selectivity in successive nucleophilic and electrophilic allylations of chiral 1,3-diols: protecting-group-free synthesis of substituted pyrans
Q26749672Contemporary Strategies for the Synthesis of Tetrahydropyran Derivatives: Application to Total Synthesis of Neopeltolide, a Marine Macrolide Natural Product
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Q43505640Formal total synthesis of the algal toxin (-)-polycavernoside A.
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Q41898437The stereodivergent formation of 2,6-cis and 2,6-trans-tetrahydropyrans: experimental and computational investigation of the mechanism of a thioester oxy-Michael cyclization.
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