SYNTHESIS OF 3-HYDROXY-3-CYCLOBUTENE-1,2-DIONE BASED AMINO-ACIDS

[1] RELATIVE REACTIVITIES OF VARIOUS SULFIDES, SELENIDES AND HALIDES TOWARDS SH2 ATTACK BY TRIBUTYLTIN RADICALS [J]. AUSTRALIAN JOURNAL OF CHEMISTRY, 1986, 39 (01) : 77 - 87

[2] FENGL RW, THESIS EMORY U

[3] KEMP JA, 1988, P NATL ACAD SCI USA, V35, P6547

[4] A FACILE SYNTHESIS OF 1-HYDROXY-2-PHOSPHONOCYCLOBUTENEDIONE [J]. TETRAHEDRON LETTERS, 1992, 33 (28) : 3961 - 3962

[5] BIOISOSTERIC REPLACEMENT OF THE ALPHA-AMINO CARBOXYLIC-ACID FUNCTIONALITY IN 2-AMINO-5-PHOSPHONOPENTANOIC ACID YIELDS UNIQUE 3,4-DIAMINO-3-CYCLOBUTENE-1,2-DIONE CONTAINING NMDA ANTAGONISTS [J]. JOURNAL OF MEDICINAL CHEMISTRY, 1992, 35 (25) : 4720 - 4726

[6] SYNTHESIS OF ALKYL SUBSTITUTED CYCLOBUTENEDIONES BY FREE-RADICAL CHEMISTRY - CARBON FOR NITROGEN REPLACEMENT IN THE ALPHA-AMINO-ACID BIOISOSTERE - 3,4-DIAMINO-3-CYCLOBUTENE-1,2-DIONE [J]. TETRAHEDRON LETTERS, 1993, 34 (17) : 2715 - 2718

[7] AN IMPROVED METHOD FOR THE SYNTHESIS OF SUBSTITUTED CYCLOBUTENEDIONES [J]. JOURNAL OF ORGANIC CHEMISTRY, 1988, 53 (11) : 2482 - 2488

[8] 3-STANNYLCYCLOBUTENEDIONES AS NUCLEOPHILIC CYCLOBUTENEDIONE EQUIVALENTS - SYNTHESIS OF SUBSTITUTED CYCLOBUTENEDIONES AND CYCLOBUTENEDIONE MONOACETALS AND THE BENEFICIAL EFFECT OF CATALYTIC COPPER IODIDE ON THE STILLE REACTION [J]. JOURNAL OF ORGANIC CHEMISTRY, 1990, 55 (19) : 5359 - 5364

[9] 4,4'-BI(CYCLOBUTENE-1,2-DIONES) - BISQUARYLS [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1993, 115 (20) : 9048 - 9055

[10] DL-TETRAZOL-5-YLGLYCINE, A HIGHLY POTENT NMDA AGONIST - ITS SYNTHESIS AND NMDA RECEPTOR EFFICACY [J]. JOURNAL OF MEDICINAL CHEMISTRY, 1992, 35 (24) : 4608 - 4612

[1] RELATIVE REACTIVITIES OF VARIOUS SULFIDES, SELENIDES AND HALIDES TOWARDS SH2 ATTACK BY TRIBUTYLTIN RADICALS [J]. AUSTRALIAN JOURNAL OF CHEMISTRY, 1986, 39 (01) : 77 - 87

[2] FENGL RW, THESIS EMORY U

[3] KEMP JA, 1988, P NATL ACAD SCI USA, V35, P6547

[4] A FACILE SYNTHESIS OF 1-HYDROXY-2-PHOSPHONOCYCLOBUTENEDIONE [J]. TETRAHEDRON LETTERS, 1992, 33 (28) : 3961 - 3962

[5] BIOISOSTERIC REPLACEMENT OF THE ALPHA-AMINO CARBOXYLIC-ACID FUNCTIONALITY IN 2-AMINO-5-PHOSPHONOPENTANOIC ACID YIELDS UNIQUE 3,4-DIAMINO-3-CYCLOBUTENE-1,2-DIONE CONTAINING NMDA ANTAGONISTS [J]. JOURNAL OF MEDICINAL CHEMISTRY, 1992, 35 (25) : 4720 - 4726

[6] SYNTHESIS OF ALKYL SUBSTITUTED CYCLOBUTENEDIONES BY FREE-RADICAL CHEMISTRY - CARBON FOR NITROGEN REPLACEMENT IN THE ALPHA-AMINO-ACID BIOISOSTERE - 3,4-DIAMINO-3-CYCLOBUTENE-1,2-DIONE [J]. TETRAHEDRON LETTERS, 1993, 34 (17) : 2715 - 2718

[7] AN IMPROVED METHOD FOR THE SYNTHESIS OF SUBSTITUTED CYCLOBUTENEDIONES [J]. JOURNAL OF ORGANIC CHEMISTRY, 1988, 53 (11) : 2482 - 2488

[8] 3-STANNYLCYCLOBUTENEDIONES AS NUCLEOPHILIC CYCLOBUTENEDIONE EQUIVALENTS - SYNTHESIS OF SUBSTITUTED CYCLOBUTENEDIONES AND CYCLOBUTENEDIONE MONOACETALS AND THE BENEFICIAL EFFECT OF CATALYTIC COPPER IODIDE ON THE STILLE REACTION [J]. JOURNAL OF ORGANIC CHEMISTRY, 1990, 55 (19) : 5359 - 5364

[9] 4,4'-BI(CYCLOBUTENE-1,2-DIONES) - BISQUARYLS [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1993, 115 (20) : 9048 - 9055

[10] DL-TETRAZOL-5-YLGLYCINE, A HIGHLY POTENT NMDA AGONIST - ITS SYNTHESIS AND NMDA RECEPTOR EFFICACY [J]. JOURNAL OF MEDICINAL CHEMISTRY, 1992, 35 (24) : 4608 - 4612