Rapid synthesis of cyclopeptide alkaloid-like para-cyclophanes by combined use of Ugi-4CR and intramolecular SNAr reaction

[1] Pd-assisted multicomponent synthesis of heterocycles [J]. EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2003, 2003 (21) : 4101 - 4111

[2] Banfi L., 2005, ORG REACTIONS, V65, P1, DOI [10.1002/0471264180.or065.01, DOI 10.1002/0471264180.0R065.01]

[3] Bienaymé H, 2000, CHEM-EUR J, V6, P3321, DOI 10.1002/1521-3765(20000915)6:18<3321::AID-CHEM3321>3.0.CO

[4] 2-A

[5] Exploiting the dual reactivity of o-isocyanobenzamide:: Three-component synthesis of 4-imino-4H-3,1-benzoxazines [J]. ORGANIC LETTERS, 2005, 7 (23) : 5285 - 5288

[6] Total synthesis of Mauritines A, B, C, and F: Cyclopeptide alkaloids with a 1-4-membered paracyclophane unit [J]. CHEMISTRY-A EUROPEAN JOURNAL, 2005, 11 (09) : 2668 - 2679

[7] Solid-phase synthesis of natural product-like macrocycles by a sequence of Ugi-4CR and SNAr-based cycloetherification [J]. TETRAHEDRON LETTERS, 2003, 44 (30) : 5575 - 5578

[8] Rapid and diverse route to natural product-like biaryl ether containing macrocycles [J]. TETRAHEDRON, 2003, 59 (40) : 7859 - 7870

[9] A rapid access to biaryl ether containing macrocycles by pairwise use of Ugi 4CR and intramolecular SNAr-based cycloetherification [J]. ORGANIC LETTERS, 2001, 3 (25) : 4079 - 4082

[10] DEGREEF M, COMMUNICATION

[1] Pd-assisted multicomponent synthesis of heterocycles [J]. EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2003, 2003 (21) : 4101 - 4111

[2] Banfi L., 2005, ORG REACTIONS, V65, P1, DOI [10.1002/0471264180.or065.01, DOI 10.1002/0471264180.0R065.01]

[3] Bienaymé H, 2000, CHEM-EUR J, V6, P3321, DOI 10.1002/1521-3765(20000915)6:18<3321::AID-CHEM3321>3.0.CO

[4] 2-A

[5] Exploiting the dual reactivity of o-isocyanobenzamide:: Three-component synthesis of 4-imino-4H-3,1-benzoxazines [J]. ORGANIC LETTERS, 2005, 7 (23) : 5285 - 5288

[6] Total synthesis of Mauritines A, B, C, and F: Cyclopeptide alkaloids with a 1-4-membered paracyclophane unit [J]. CHEMISTRY-A EUROPEAN JOURNAL, 2005, 11 (09) : 2668 - 2679

[7] Solid-phase synthesis of natural product-like macrocycles by a sequence of Ugi-4CR and SNAr-based cycloetherification [J]. TETRAHEDRON LETTERS, 2003, 44 (30) : 5575 - 5578

[8] Rapid and diverse route to natural product-like biaryl ether containing macrocycles [J]. TETRAHEDRON, 2003, 59 (40) : 7859 - 7870

[9] A rapid access to biaryl ether containing macrocycles by pairwise use of Ugi 4CR and intramolecular SNAr-based cycloetherification [J]. ORGANIC LETTERS, 2001, 3 (25) : 4079 - 4082

[10] DEGREEF M, COMMUNICATION