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- [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] IWASAWA N, 1987, CHEM LETT
- [6] ALPHA,BETA-UNSATURATED ORTHO-ESTERS AS MICHAEL ACCEPTORS - THE TRITYL SALT-CATALYZED MICHAEL REACTION OF ALPHA,BETA-UNSATURATED ORTHO-ESTERS WITH SILYL ENOL ETHERS[J]. CHEMISTRY LETTERS, 1987, (06) : 1183 - 1186KOBAYASHI, SMUKAIYAMA, T
- [7] TRITYL SALTS AS EFFICIENT CATALYSTS IN THE ALDOL REACTION[J]. CHEMISTRY LETTERS, 1985, (10) : 1535 - 1538KOBAYASHI, SMURAKAMI, MMUKAIYAMA, T
- [8] AN EFFICIENT AND EXTREMELY MILD CATALYST SYSTEM, COMBINED USE OF TRITYL CHLORIDE AND TIN(II) CHLORIDE, IN THE ALDOL AND MICHAEL REACTIONS[J]. CHEMISTRY LETTERS, 1987, (03) : 491 - 494MUKAIYAMA, TKOBAYASHI, STAMURA, MSAGAWA, Y
- [9] 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
- [10] A FACILE SYNTHESIS OF ALPHA-GLUCOSIDES AND ALPHA-RIBOSIDES FROM THE CORRESPONDING 1-O-ACYL SUGARS AND ALCOHOLS IN THE PRESENCE OF TRITYL PERCHLORATE[J]. CHEMISTRY LETTERS, 1984, (06) : 907 - 910MUKAIYAMA, TKOBAYASHI, SSHODA, S