共 9 条
- [1] ENANTIOSELECTIVE MICHAEL REACTIONS - STEREOSELECTIVE ADDITION OF ENOLATES OF PHENMENTHOL ESTERS TO CROTONATES[J]. TETRAHEDRON LETTERS, 1985, 26 (41) : 5025 - 5028COREY, EJPETERSON, RT
- [2] ASYMMETRIC MICHAEL ADDITIONS VIA SAMP-HYDRAZONES RAMP-HYDRAZONES ANTI-DIASTEREO-SELECTIVE AND ENANTIOSELECTIVE SYNTHESIS OF 3,4-DISUBSTITUTED 5-OXO-ALKANOATES[J]. TETRAHEDRON LETTERS, 1986, 27 (30) : 3491 - 3494ENDERS, DPAPADOPOULOS, KRENDENBACH, BEMAPPEL, RKNOCH, F
- [3] THE OXIDATIVE MICHAEL REACTION - A HIGHLY DIASTEREOSELECTIVE SYNTHESIS OF 5-OXOCARBOXYLIC ACID-DERIVATIVES[J]. CHEMISTRY LETTERS, 1986, (09) : 1623 - 1626HASHIMOTO, YMUKAIYAMA, T
- [4] OXIDATIVE COUPLING OF KETENE DITHIOACETALS WITH SILYLATED CARBON NUCLEOPHILES BY THE USE OF TRITYL TETRAFLUOROBORATE[J]. CHEMISTRY LETTERS, 1986, (05) : 755 - 758HASHIMOTO, YMUKAIYAMA, T
- [5] THE HIGHLY STEREOSELECTIVE MICHAEL REACTION OF ALPHA,BETA-UNSATURATED KETONES WITH SILYL ENOL ETHERS OF THIOESTERS CATALYZED BY TRITYL SALTS - A FACILE STEREOSELECTIVE SYNTHESIS OF 5-OXOCARBOXYLIC ACID ESTER DERIVATIVES[J]. CHEMISTRY LETTERS, 1986, (11) : 1817 - 1820MUKAIYAMA, TTAMURA, MKOBAYASHI, S
- [6] NARASAKA K, 1976, B CHEM SOC JPN, V49, P779, DOI 10.1246/bcsj.49.779
- [7] MICHAEL TYPE REACTION OF O-SILYLATED KETENE ACETALS WITH ALPHA,BETA-UNSATURATED CARBONYL-COMPOUNDS PROMOTED BY TITANIUM TETRACHLORIDE[J]. CHEMISTRY LETTERS, 1976, (02) : 163 - 164SAIGO, KOSAKI, MMUKAIYAMA, T
- [8] STETTER H, 1973, SYNTHESIS-STUTTGART, P207
- [9] A HIGHLY STEREOSELECTIVE MICHAEL REACTION OF SIMPLE ESTER ENOLATES TO ALPHA,BETA-UNSATURATED ESTERS[J]. TETRAHEDRON LETTERS, 1984, 25 (49) : 5661 - 5664YAMAGUCHI, MTSUKAMOTO, MTANAKA, SHIRAO, I