RSS-Feed abonnieren
DOI: 10.1055/s-0029-1219180
Efficient Construction of the Carbon Skeleton of the Novel Polyoxazole-Based Cyclopeptide IB-01211 via a Biomimetic Macrocyclisation
Publikationsverlauf
Publikationsdatum:
08. Januar 2010 (online)
Abstract
An efficient construction of the entire carbon skeleton of the novel polyoxazole-based natural product IB-01211 was developed which featured a biomimetic macrocyclisation of an ω-amino acid tethered through two bisoxazole units as the key step.
Key words
heterocycles - biomimetic - macrocyclisation - peptides - oxazoles
- For reviews see:
-
1a
Pattenden G. J. Heterocycl. Chem. 1992, 29: 607 -
1b
Faulkner DJ. Nat. Prod. Rep. 2002, 29: 1 ; and earlier reports in the series -
1c
Yeh VSC. Tetrahedron 2004, 60: 11995 -
1d
Bertram A.Pattenden G. Nat. Prod. Rep. 2007, 24: 18 -
1e
Hughes RA.Moody CJ. Angew. Chem. Int. Ed. 2007, 46: 2 - For some examples, see:
-
2a
Gonzalez MA.Pattenden G. Angew. Chem. Int. Ed. 2003, 42: 1255 -
2b
Krebs O.Taylor RJK. Org. Lett. 2005, 7: 1063 -
2c
Bagley MC.Chapaneri K.Dale JW.Xiong X.Bower J. J. Org. Chem. 2005, 70: 1389 -
2d
Bagley MC.Bashford KE.Hesketh CL.Moody CJ. J. Am. Chem. Soc. 2000, 122: 3301 -
2e
Mann E.Kessler H. Org. Lett. 2003, 5: 4567 -
2f
Burgett AWG.Li Q.Wei Q.Harran PG. Angew. Chem. Int. Ed. 2003, 42: 4961 -
2g
Liu P.Panek JS. J. Am. Chem. Soc. 2000, 122: 1235 - 3
Deeley J.Pattenden G. Chem. Commun. 2005, 797 - 4
Kanoh K.Matsuo Y.Adachi K.Imagawa H.Nishizawa M.Shizuri Y. J. Antibiot. 2005, 58: 289 - 5
Shin-Ya K.Weirzba K.Matsuo K.Ohtani T.Yamada Y.Furihata K.Hayakawa Y.Seto HJ. J. Am. Chem. Soc. 2001, 123: 1262 - 6
Wipf P. Chem. Rev. 1995, 95: 2115 - 7
Chattopadhyay SK.Pattenden G. Synlett 1997, 1342 -
8a
Pattenden G.Ashweek NJ.Baker-Glenn CAG.Walker GM.Yee JGK. Angew. Chem. Int. Ed. 2007, 46: 4359 -
8b
Pattenden G.Ashweek NJ.Baker-Glenn CAG.Kempson J.Walker GM.Yee JGK. Org. Biol. Chem. 2008, 6: 1478 -
9a For
related contemporaneous studies, see:
Doi T.Yoshida M.Shin-Ya K.Takahasi T. Org. Lett. 2006, 8: 4165 -
9b
Deeley J.Bertram A.Pattenden G. Org. Biol. Chem. 2008, 6: 1994 -
9c
Marson MC.Saadi M. Org. Biol. Chem. 2006, 4: 3892 - 10
Chattopadhyay SK.Biswas S. Tetrahedron Lett. 2006, 47: 7897 - 11
Romero F,Malet L,Canedo LM,Cuevas C, andReyes J. inventors; WO 2005/000880 A2. -
12a
Hernández D.Vilar G.Riego E.Cañedo LM.Cuevas C.Albericio F.Álvarez M. Org. Lett. 2007, 9: 809 -
12b
Hernández D.Riego E.Francesch A.Cuevas C.Albericio F.Álvarez M. Tetrahedron 2007, 63: 9862 -
12c
Hernández D.Riego E.Albericio F.Álvarez M. Eur. J. Org. Chem. 2008, 3389 - 13
Chattopadhyay SK.Biswas S.Ghosh SK. Synthesis 2008, 7897 - 14
Chattopadhyay SK.Biswas S.Pal BK. Synthesis 2006, 1289 - 15
Wipf P.Miller CP. J. Org. Chem. 1993, 58: 3604 -
17a
Chattopadhyay SK.Kempson J.McNeil A.Pattenden G.Reader M.Rippon DE.Waite D. J. Chem. Soc., Perkin Trans. 1 2000, 2415 -
17b
Endo N.Tsuboi K.Kim R.Yonezawa Y.Shin C. Heterocycles 2003, 60: 1567
References and Notes
All new compounds reported here gave
satisfactory spectroscopic and/or analytical data.
Data for 27
Mp 144-146 ˚C.
IR (KBr): 3367, 2927, 1683, 1652, 1515, 1259, 1114, 766 cm-¹. ¹H
NMR (400 MHz, CDCl3): δ = 9.46 (s,
1 H), 8.61 (d, J = 8.4
Hz, 1 H), 8.35 (s, 1 H), 8.27 (s, 1 H), 8.14 (s, 1 H), 8.13 (d, J = 7.2 Hz,
1 H), 7.64-7.62 (m, 2 H), 7.49-7.43 (m, 6 H),
7.40-7.38 (m, 4 H), 7.36-7.33 (m, 3 H), 6.88 (s,
1 H), 6.01 (dd, J = 6.8
Hz, 1 H), 5.97 (s, 1 H), 5.34-5.28 (m, 1 H), 4.63 (dd, J = 8.0, 4.8
Hz, 1 H), 4.10 (dd J = 9.2,
5.6 Hz, 1 H), 3.97-3.92 (m, 1 H), 3.73 (t J = 9.2
Hz, 1 H), 2.42-2.37 (m, 1 H), 1.90-1.87 (m, 1
H), 1.03-0.99 (m, 15 H), 0.90-0.86 (m, 2 H), 0.80
(d, J = 6.8
Hz, 3 H), 0.65 (t, J = 7.2
Hz, 3 H). ¹³C NMR (100 MHz, CDCl3): δ = 171.7
(s), 169.9 (s), 164.5 (s), 160.3 (s), 159.1 (s), 158.6 (s), 154.6
(s), 152.1 (s), 151.6 (s), 141.8 (d), 139.3 (d), 139.1 (d), 137.3
(s), 135.0 (d), 134.9 (d), 132.7 (s), 132.6 (s), 132.2 (s), 131.8
(s), 130.4 (d), 130.3 (s), 129.9 (d), 129.8 (d), 129.5 (s), 128.5
(d), 128.3 (d), 127.8 (d), 127.7 (d), 126.0 (s), 105.2 (t), 64.7
(t), 59.8 (d), 56.4 (d), 49.3 (d), 38.2 (d), 29.2 (d), 26.3 (q),
24.7 (t), 19.8 (q), 18.7 (q), 18.3 (s), 14.9 (q), 11.1 (q). HRMS (TOFMS
ES+): m/z [M+ + Na] calcd
for C51H54N8NaO9Si: 973.3681;
found: 973.3682