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1.
An enantioselective synthesis of (+)-prelactone B 1 has been achieved on a multigram scale starting from a known bicyclic precursor 2. The key feature of the strategy is the generation of 3-stereogenic centres from a single bicyclic precursor, which has been utilized as a chiral building block for the synthesis of various natural products. 相似文献
2.
Clay catalyzed Friedländer condensation of 2-amino arylaldehyde or ketone with carbonyl compounds containing α-methylene group has been achieved in solvent free condition under microwave irradiation to give polycyclic quinoline derivatives. 相似文献
3.
Asymmetric total synthesis of the sex pheromones of Japanese beetle and currant stem girdler, (R)‐japonilure (1) and (4R,9Z)‐9‐octadecen‐4‐olide (2), has been achieved. 相似文献
4.
Cerium(III) chloride heptahydrate (CeCl3·7H2O) catalyzes the reaction of substituted salicylaldehydes with 1,3-cyclohexane dione or dimedone in aqueous medium at reflux temperature to afford the corresponding 1-oxo-1,2,3,4,9,10-hexahydroxanthene derivatives4 0 in high yields. 相似文献
5.
Stereoselective total synthesis of two chiral lactones, (+)‐trans‐cognac lactone (1b) and (+)‐trans‐aerangis lactone (2c), has been achieved from the same intermediate using a radical‐based cyclization route. 相似文献
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The first total synthesis of Pestalotioprolide C and C7-epi-Pestalotioprolide C adopting Noyori asymmetric reduction, HWE Olefination and Shiina macrolactonization as the key steps has been described. 相似文献
8.
Gowravaram Sabitha Kurra Yadagiri Martha Bhikshapathi Gajangi Chandrashekhar Jhillu Singh Yadav 《Tetrahedron: Asymmetry》2010,21(20):2524-2529
The construction of the C32–C42 fragment of etnangien is described using a desymmetrization strategy generating five stereogenic centers from a bicyclic lactone. Another notable feature includes the use of the Sharpless asymmetric epoxidation to generate a stereogenic center at C40. 相似文献
9.
Gowravaram Sabitha Narjis Fatima Peddabuddi Gopal C. Nagendra Reddy Jhillu S. Yadav 《Tetrahedron: Asymmetry》2009,20(2):184-191
Prins and olefin cross-metathesis reactions were used as the key steps for the stereoselective total synthesis of (+)-strictifolione and (6R)-6-[(4R,6R)-4,6-dihydroxy-10-phenyldec-1-enyl]-5,6-dihydro-2H-pyran-2-one. Removal of MOM protecting groups under neutral conditions using CeCl3·7H2O is an attractive addition to the present strategy. 相似文献
10.
Synthesis of stereoisomers of 6′‐mono‐ and 4′,6′‐di‐O‐benzyl cryptofolione is described through a key intermediate 6 , which was prepared by coupling of iodobenzene 8 with chiral propargyl alcohol 9 under Cosford protocol conditions. Monobenzyl ether 4 is obtained via epoxide 6 opening with vinyl Grignard, followed by cross‐metathesis reaction with a vinyl lactone 11 . Whereas, dibenzyl ether 5 is prepared by epoxide 6 opening with chiral propargyl alcohol 7 followed by simple transformations and finally cis‐Wittig olefination. 相似文献