Kwang-Deuk Lee, Jang-Min Suh, Jae-Hoon Park, Hyun-Joon Ha, Hwan Gun Choi, Chan Sun Park, Jae Won Chang, Won Koo Lee, Yongkwan Dong and Hoseop Yun                                         

 

 

Syntheses of cis-2-alkylaziridine-2-carboxylates including cis-3- henylaziridine-2-carboxylates were achieved from the reaction of α- minonitrile and alkyldiazoacetate in the presence of a Lewis acid. Asymmetric version of this reaction with the chiral α-methylbenzylamine was also successful for the preparation of chiral aziridines that were used for the synthesis of various amino acids including homophenylalanine, β-amino-α-hydroxy acid, and α-amino-β-hydroxy acid via regioselective aziridine ring openings.

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List of Articles
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28 28. Synthesis and SAR of Aziridinylquinoline-5,8-diones as Agents against Malignant Tumor Cells - Bull. Kor. Chem. Soc. 2001, 22, 1067 imagefile aziridine 2010-05-12 3307
27 27. Synthesis of Substituted-(l)-Tryptophanols from an Enantiomerically Pure Aziridine-2-methanol - Org. Lett. 2001, 3, 4197. imagefile aziridine 2010-05-12 3461
26 26. New Uses of Amino Acids as Chiral Building Blocks in Organic Synthesis - Org. Lett. 2001, 3, 3119 imagefile aziridine 2010-05-12 3440
25 25. Asymmetric synthesis of β-amino-α-hydroxy acids through Lewis acid-mediated addition of ketone acetal to imines - Bull. Chem. Soc. Jpn. 2001, 74, 1667 imagefile aziridine 2010-05-12 4104
» 24. New synthesis and ring opening of cis-3-alkylaziridine-2-carboxylates - Tetrahedron 2001, 57, 9655 imagefile aziridine 2010-05-12 4072
23 23. Synthesis of Quaternary Ammoniocephalosporin Having Two Vinyl Groups Using Radical Promoted Thermal Isomerization - Bull. Kor. Chem. Soc. 2001, 22, 659 imagefile aziridine 2010-05-12 3437
22 22. Selective production of difluoromethyl methyl ether from chlorodifluoromethane using alkali metal carbonates - J. Fluorine Chem. 2001, 107, 133 imagefile aziridine 2010-05-12 4322
21 21. Cycloaddition of Lewis Acid-Induced N-Methyleneanilines as Azadienes to 1,2-Bistrimethylsilyloxycyclobutene and Oxidative Ring Expansion to 1,2,4,5-Tetrahydro-1-benzazocine-3,6-diones - J. Org. Chem. 2000, 65, 8384 imagefile aziridine 2010-05-12 3423
20 20. Stereoselective synthesis of enantiomerically pure D-threo-PDMP; manipulation of a core 2,3-diamino alcohol unit - Tetrahedron : Asymmetry 2000, 11, 3283 imagefile aziridine 2010-05-12 3340
19 19. Stereoselective synthesis of protected threo-β-hydroxy-L-glutamic acid using a chiral aziridine - Tetrahedron : Asymmetry 2000, 11, 3283 imagefile aziridine 2010-05-12 3705
18 18. Preparation of Cysteinol Derivatives by Highly Regioselective Ring Opening Nonactivated Chiral Aziridines by Thiols - Tetrahedron 1999, 55, 10041 imagefile aziridine 2010-05-12 3515
17 17. The Thiazole Route to 2-Formyl-1β-Methylcarbapenem - Bull. Kor. Chem. Soc. 1998, 19, 1294 imagefile aziridine 2010-05-12 3147
16 16. Synthesis of Substituted (D)-Phenylalanine Derivatives by Regioselective Reduction of Enantiomerically Pure cis-2,3-Disubstituted Aziridines - Tetrahedron Lett. 1998, 39, 9193 imagefile aziridine 2010-05-12 3402
15 15. Preparation of both (D)- and (L)-serinol derivatives from N-[(S)-a-methylbenzyl]-aziridine-2(S)-methanol - Heterocycles 1998, 48, 1917 imagefile aziridine 2010-05-12 3174
14 14. A new synthetic route to (3R,4S)-3-hydroxy-4-phenylazetidin-2-one as a taxol side chain precursor - Tetrahedron : Asymmetry 1998, 9, 983 imagefile aziridine 2010-05-12 2966
13 13. Efficient Syntheses of (1R,2R)- and (1S,2S)-2-Amino-1-alkyl(oraryl)-1,3-propanediols by Regioselective Ring Opening of Aziridine-2-methanols - J. Org. Chem. .1997, 743 imagefile aziridine 2010-05-12 3479
12 12. Highly diastereoselective reduction of enantiomerically pure aziridino ketones - Tetrahedron 1996, 52, 12117 imagefile aziridine 2010-05-06 3152
11 11. An Effcient synthesis of both enantiomers of cathinone by regioselective reductive ring opening of substituted aziridines - Tetrahedron 1996, 52, 12111 imagefile aziridine 2010-05-06 3174
10 10. Efficient Synthesis of Ephedra Alkaloid Analogues Using an Enantiomerically Pure N-[(R)-(+)-r-Methylbenzyl]aziridine-2-carboxaldehyde - J. Org. Chem. 1996, 61, 6183 imagefile aziridine 2010-05-06 3264
9 9. Resiospecific reductive ring cleavage of N-substituted aziridine-2-carboxylates and an aziridine-2-methanol via catalytic hydrogenation using Pd as a catalyst - Tetrahedron Lett. 1995, 36, 8431 imagefile aziridine 2010-05-06 3137
8 8. Chirospecific Syntheses of Precursors of Cyclopentane and cyclopentene Carbocyclic Nucleosides by [3 + 33-Coupling and Transannular Alkylation - J. Org. Chem. 1995, 60, 4602 imagefile aziridine 2010-05-06 3254
7 7. Regioselective N-Methyl Carbon Lithiation of N-Boc-MethylalkylaminrylamiEnxepae dient Synthesis of Unsymmetrical Amines - Tetrahedron Lett. 1994, 35, 4067 imagefile aziridine 2010-05-06 3112
6 6. Chirospecific Synthesis of (1S,3R)-l-Amino-3-(hydroxymethyl)cyclopentane a Precursor for Carbocyclic Nucleoside Synthesis. Intramolecular Aziridine Cyclizations - J. Org. Chem. 1993, 58, 5019 imagefile aziridine 2010-05-06 3005
5 5. a-Lithioamine Synthetic Equivalents: Syntheses of Diastereoisomers from Boc Derivatives of Cyclic Amines - J. Org. Chem. 1993, 58, 1109 imagefile aziridine 2010-05-06 2998
4 4. Endocyclic Restriction Test: Evaluation of Transition-Structure Geometry for an Aryl Bromide-Alkyllithium Exchange Reaction - J. Am. Chem. Soc. 1990, 112, 1629 imagefile aziridine 2010-05-06 2904
3 3. a-Lithioamine Synthetic Equivalents: Syntheses of Diastereoisomers from the Boc Piperidines - J. Org. Chem. 1990, 55, 2578 imagefile aziridine 2010-05-06 2816
2 2. a-Lithioamine synthetic equivalents from dipole-stabilized carbaniones: The r-Boc group as an activator for a’-Lithiation of carbamates - Tetrahedron Lett. 1989, 30, 1197 imagefile aziridine 2010-05-06 2305
1 1. Regiospecific Alkylation of Allylic Halides with Latent-γ-Functionality - J. Org. Chem. 1984, 49, 1838 imagefile aziridine 2010-05-06 2308


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