1958
DOI: 10.1021/ja01535a030
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A Preparation and Some of the Properties of trans-6,14-Dihydrolevopimaric Acid-6,14-endo-α,β-succinic Acid

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Cited by 23 publications
(6 citation statements)
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“…14 Fumaropimaric acid 3 was prepared according to the reported procedure. 15 The conversion of trimethyl esters to triols 4 and 5 was carried out by the reported procedure 16 and followed by ring closure with (R)-or (S)-ditosylate 1 in the presence of NaH in THF under high dilution conditions. In the final step, four 1,1 0 -binaphthyl-appended crown ethers were obtained via a regioselective ring formation reaction (Scheme 2) in over 11% yield.…”
Section: Synthesismentioning
confidence: 99%
“…14 Fumaropimaric acid 3 was prepared according to the reported procedure. 15 The conversion of trimethyl esters to triols 4 and 5 was carried out by the reported procedure 16 and followed by ring closure with (R)-or (S)-ditosylate 1 in the presence of NaH in THF under high dilution conditions. In the final step, four 1,1 0 -binaphthyl-appended crown ethers were obtained via a regioselective ring formation reaction (Scheme 2) in over 11% yield.…”
Section: Synthesismentioning
confidence: 99%
“…Nowadays, rosin and its Diels-Alder adducts have been developed as a feedstock for synthesizing various chemicals and intermediates. Maleopimaric acid was isolated from maleic anhydride modified rosin (Halbrook & Lawrence, 1958), and its crystal structure has been reported (Rao et al, 2008). The title compound C 24 H 40 O 3 .…”
Section: S1 Commentmentioning
confidence: 99%
“…For various applications of rosin, see: Halbrook & Lawrence (1958). For the separation of the title compound, see: Aldrich (1971); Halbrook & Lawrence (1959); Song et al (2009).…”
Section: Related Literaturementioning
confidence: 99%
“…As an abundant and renewable material, rosin is mainly known as additives and modifiers for various applications (Halbrook et al, 1958). Fumaric modified rosin is one of modified products of rosin.…”
Section: S1 Commentmentioning
confidence: 99%