排序方式: 共有12条查询结果,搜索用时 31 毫秒
1.
Armando Talavera-Alemán Mario A. Gómez-Hurtado Rosa E. del Río Jérôme Marrot Christine Thomassigny Christine Greck 《Tetrahedron letters》2017,58(30):2901-2903
The first study of photooxidation reaction of 6β-acetoxyvouacapane isolated from Caesalpinia platyloba is reported. The reaction yielded four new epoxy lactones, 6β-acetoxy-15,16α-epoxy-13-spirocassa-12,16-olide, 6β-acetoxy-15,16β-epoxy-13-spirocassa-12,16-olide, 6β-acetoxy-12,13β-epoxycassa-16,12-olide and 6β-acetoxy-12,13α-epoxycassa-16,12-olide. All the structures were supported by 1D and 2D NMR spectroscopy as well as mass spectrometry. The stereochemistry was established on the base of single crystal X-ray diffraction. 相似文献
2.
Formation of three diasteroisomeric spirodilactones 14a-c and 11 has been reported from diester 13 and 9, respectively, under the influence of mineral acid. 相似文献
3.
Nicholas A. Weires Yuriy Slutskyy Larry E. Overman 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2019,131(25):8649-8653
An alkoxycarbonyl radical cyclization–cross‐coupling cascade has been developed that allows functionalized γ‐butyrolactones to be prepared in one step from simple tertiary alcohol‐derived homoallylic oxalate precursors. The reaction succeeds with aryl and vinyl electrophiles and is compatible with heterocyclic fragments in both coupling partners. This chemistry allows for the rapid construction of spirolactones, which are of interest in drug discovery endeavors. 相似文献
4.
A concise stereoselective synthesis of 3-spiro-α-methylene-γ-butyrolactone oxindoles from Morita-Baylis-Hillman adducts of isatin in excellent yield has been achieved following a three-step reaction sequences viz. (1) Isomerisation of the Morita-Baylis-Hillman adducts of isatin with trimethyl orthoformate and montmorillonite K10 clay catalyst, (2) a second Morita-Baylis-Hillman reaction with formaldehyde, and (3) an acid catalysed lactonization. The structure and stereochemistry of the products were assigned by X-ray crystallographic and NMR spectroscopic studies. Formation and mechanism of the minor product spirofuran oxindoles and a one-pot base promoted second Morita-Baylis-Hillman adduct formation-lactonization reaction have also been achieved. 相似文献
5.
A dual pathway from readily available 2-allyl-2-carboethoxycycloalkanones 1 provides a new facile stereoselective synthesis either of functionalized spiro ketolactones 4 or of ring enlarged lactones 7 in one-step. Thus, iodination of 5-8-membered 2-allyl-2-carboethoxycycloalkanones 1a-d led, in excellent yields, to spiro ketolactones 4a-d, respectively, as single stereoisomers. On the other hand, iodination of 1a-d under alkoxy radical fragmentation conditions via incipient hemiketals produced the 8-, 9-, 10-, or 11-membered, three-atom ring enlarged, poly-functionalized lactones 7a-c as two stereoisomers and 8 as a single isomer. 相似文献
6.
Several novel benzofuran-containing spirolactones were synthesized and characterized using copper-catalyzed heterodimerization of 1,2-diarylcyclopropenones, and followed by sequential intramolecular cyclopropene ring opening and oxidative cyclization. 相似文献
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8.
Raju KarmakarDipakranjan Mal 《Tetrahedron letters》2011,52(46):6098-6102
α-Methylene-α-tetralone dimers (8-10) are shown to undergo a diastereoselective Prins reaction with paraformaldehyde in the presence of N-methylanilinium trifluoroacetate resulting in 2, 4, and 5. The structure of the new scaffold 2 was confirmed by X-ray crystallographic analysis. 相似文献
9.
We demonstrate here the rational design of a conformationally flexible C2-symmetric iodosylarene 8g based on secondary n-σ∗ or hydrogen-bonding interactions as a chiral catalyst for the enantioselective Kita oxidative spirolactonization of 1-naphthol derivatives 5. Iodosylarenes 8 were generated in situ from iodoarenes 7 and mCPBA as a co-oxidant. Furthermore, epoxyspirolactone 15 was obtained by the one-pot oxidation of 5 with mCBPA in the presence of 7g. Thus, the enantioselective oxidation of 5 to 6 and the successive enantio- and diastereo-selective oxidation of 5 to 15 proceeded in good yields when we controlled the amount of mCPBA. 相似文献
10.
Katja Dahms 《Tetrahedron letters》2010,51(50):6605-6607
The reaction of diphenyl sulfone with 2,3-dibromophthalazine-1,4-dione in the presence of n-butyllithium gave a spiro-9H-thioxanthene-10,10-dioxide derivative in 45% yield, the structure of which was proved by X-ray crystallography. 相似文献