Subscribe to RSS
Please copy the URL and add it into your RSS Feed Reader.
https://www.thieme-connect.de/rss/thieme/en/10.1055-s-00000083.xml
Synlett 2006(1): 0023-0032
DOI: 10.1055/s-2005-921930
DOI: 10.1055/s-2005-921930
ACCOUNT
© Georg Thieme Verlag Stuttgart · New York
The Ever-Challenging Quassinoids
Further Information
Received
23 August 2005
Publication Date:
16 December 2005 (online)
Publication History
Publication Date:
16 December 2005 (online)
Abstract
The evolution of a synthetic approach to the challenging targets quassinoids is described.
1 Introduction
2 The Diels-Alder Reaction as a Key Feature
2.1 Intermolecular Diels-Alder
2.2 Intramolecular Diels-Alder
2.3 Unsuccessful Diels-Alder Cycloadditions
3 The Diene-Transmissive Approach to Quassinoids
3.1 Without the C10 Methyl Group
3.2 With the C10 Methyl Group
4 A Successful Sequence
5 Conclusion and Outlook
Key words
quassinoids - Simaroubacea - diene-transmissive Diels-Alder cycloaddition - vinylallenes - SN2′ displacement
- For reviews on the isolation and biological activities of quassinoids, see:
-
1a
Guo Z.Vangapandu S.Sindelar RW.Walker LA.Sindelar RD. Curr. Med. Chem. 2005, 12: 173 -
1b
Okano M.Fukamiya N.Lee KH. Stud. Nat. Prod. Chem. 1990, 7: 369 -
1c
Polonsky J. J. Fortschr. Chem. Org. Naturst. 1973, 30: 101 -
1d
Polonsky J. J. Fortschr. Chem. Org. Naturst. 1985, 47: 221 -
2a
Valenta Z.Gray AH.Papadopoulos S.Podesva C. Tetrahedron Lett. 1960, 1: 25 -
2b
Valenta Z.Gray AH.Orr DE.Papadopoulos S.Podesva C. Tetrahedron 1962, 18: 1433 -
3a
Clark EP. J. Am. Chem. Soc. 1937, 59: 927 -
3b
Clark EP. J. Am. Chem. Soc. 1937, 59: 2511 - For a review on the synthetic aspect of quassinoids see:
-
4a
Kawada K.Kim M.Watt DS. Org. Prep. Proced. Int. 1989, 21: 521 -
4b
Murae T.Sasaki M. Stud. Nat. Prod. Chem. 1992, 11: 71 - Recent syntheses include:
-
4c
Walker DP.Grieco PA. J. Am. Chem. Soc. 1999, 121: 9891 -
4d
Grieco PA.Collins JL.Huffman JC. J. Org. Chem. 1998, 63: 9576 -
4e
Shing TKM.Jiang Q. J. Org. Chem. 2000, 65: 7059 -
5a
VanderRoest JM.Grieco PA. J. Org. Chem. 1996, 61: 5316 -
5b
Stojanac N.Valenta Z. Can. J. Chem. 1991, 69: 853 -
5c
Hirota H.Yokoyama A.Miyaji K.Nakamura T.Igarashi M.Takahashi T. J. Org. Chem. 1991, 56: 1119 -
5d
Kim M.Kawada K.Gross RS.Watt DS. J. Org. Chem. 1990, 55: 504 -
5e For a relay synthesis see:
Sasaki M.Murae T.Takahashi T. J. Org. Chem. 1990, 55: 528 - For selected examples see:
-
6a
Alvarez-Manzaneda EJ.Romera JL.Barrero AF.Alvarez-Manzaneda R.Chahboun R.Meneses R.Aparicio M. Tetrahedron 2005, 61: 837 -
6b
Donahue MG.Hart DJ. Can. J. Chem. 2004, 82: 314 -
6c
Spino C.Hill B.Dubé P.Gingras S. Can. J. Chem. 2003, 81: 81 -
6d
Kraus GA.Cui W. J. Org. Chem. 2002, 67: 9475 -
6e
Barriault L.Ouellet SG.Deslongchamps P. Tetrahedron 1997, 53: 14937 -
6f
Takeya T.Motegi S.Itoh T.Tobinaga S. Chem. Pharm. Bull. 1997, 45: 613 -
6g
Govindan SV.Fuchs PL. J. Org. Chem. 1988, 53: 2593 -
6h
Kerwin SM.Paul AG.Heathcock CH. J. Org. Chem. 1987, 52: 1686 -
6i
Shishido K.Takahashi K.Fukumoto K.Kametani T.Honda T. J. Org. Chem. 1987, 52: 5704 -
6j
Stevens RV.Vinogradoff AP. J. Org. Chem. 1985, 50: 4056 -
6k
Ziegler FE.Klein SI.Pati UK.Wang TF. J. Am. Chem. Soc. 1985, 107: 2730 -
6l
Batt DG.Takamura N.Ganem B. J. Am. Chem. Soc. 1984, 106: 3353 -
7a
Wiseman CL.Yap HY.Bedikian AY.Bodey GP.Blumenschein GR. Am. J. Clin. Oncol. 1982, 5: 389 -
7b
Arsenau JC.Wolter JM.Kuperminc M.Ruckdeschel JC. Invest. New Drugs 1983, 1: 239 - 8
Cuendet M.Pezzuto JM. J. Nat. Prod. 2004, 67: 269 -
9a
Polonsky J. Chemistry and Biological Activity of the Quassinoids, In The Chemistry and Chemical Taxonomy of the RutalesWaterman PG.Grandon MF. Academic Press; New York: 1983. p.247 -
9b
Lidert Z.Wing K.Polonsky J.Imakura Y.Okano M.Tani S.Lin Y.-M.Kiyokawa H.Lee K.-H. J. Nat. Prod. 1987, 50: 442 -
9c
Rahman S.Fukamiya N.Okano M.Tagahara K.Lee K.-H. Chem. Pharm. Bull. 1997, 45: 1527 -
10a
Grieco PA.Ferriño S.Vidari G. J. Am. Chem. Soc. 1980, 102: 7586 -
10b
Grieco PA.Vidari G.Ferriño S. Tetrahedron Lett. 1980, 21: 1619 - For selected examples of other total syntheses by the Grieco group, see:
-
10c
Grieco PA.Lis R.Ferriño S.Law JY. J. Org. Chem. 1984, 49: 2342 -
10d
Grieco PA.Parker DT.Nargund RP. J. Am. Chem. Soc. 1988, 110: 5568 -
10e
Grieco PA.Collins JL.Moher ED.Fleck TJ.Gross RS. J. Am. Chem. Soc. 1993, 115: 6078 -
10f
Grieco PA.Collins JL.Huffman JC. J. Org. Chem. 1998, 63: 9576 - 11
Weller DD.Stirchak EP. J. Org. Chem. 1983, 48: 4873 - 12
Stevens RV.Angle SR.Kloc K.Mak KF.Trueblood KN.Liu Y.-X. J. Org. Chem. 1986, 51: 4347 -
13a
Kraus GA.Taschner MJ.Shimagaki M. J. Org. Chem. 1982, 47: 4271 -
13b
Kraus GA.Cui W. J. Org. Chem. 2002, 67: 9475 -
14a
Stojanac N.Stojanac Z.White P.Valenta Z. Can. J. Chem. 1979, 57: 3346 -
14b
Stojanac N.Sood A.Stojanac Z.Valenta Z. Can. J. Chem. 1975, 53: 619 - 15
Kraus GA.Krolsky ME. J. Org. Chem. 1986, 51: 3347 -
16a
Shishido K.Takahashi K.Fukumoto K. J. Org. Chem. 1987, 52: 5704 -
16b
Shishido K.Saitoh T.Fukumoto K.Kametani T. J. Chem. Soc., Chem. Commun. 1983, 852 - 17
Schlessinger RH.Wong J.-W.Poss MA.Springer JP. J. Org. Chem. 1985, 50: 3950 - 18
Shing TKM.Jiang Q.Mak TCW. J. Org. Chem. 1998, 63: 2056 - 19
Herscovici J.Delatre S.Boumaïza L.Antonakis K. J. Org. Chem. 1993, 58: 3928 - 20
Mandell L.Lee DE.Courtney LF. J. Org. Chem. 1982, 47: 610 -
21a
Voyle M.Dunlap NK.Watt DS. J. Org. Chem. 1983, 48: 3242 -
21b
Voyle M.Kyler KS.Arseniyadis S.Dunlap NK.Watt DS. J. Org. Chem. 1983, 48: 470 -
22a
Blomquist AT.Verdol JA. J. Am. Chem. Soc. 1955, 77: 81 -
22b
Bailey WJ.Economy J. J. Am. Chem. Soc. 1955, 77: 1133 -
22c
Bailey WJ.Cunov CH.Nicholas L. J. Am. Chem. Soc. 1955, 77: 2787 -
23a
Tsuge O.Wada E.Kanemasa S. Chem. Lett. 1983, 239 -
23b
Tsuge O.Wada E.Kanemasa S.Sakoh H. Bull. Chem. Soc. Jpn. 1984, 57: 3221 -
23c
Tsuge O.Kanemasa S.Sakoh H.Wada E. Bull. Chem. Soc. Jpn. 1984, 57: 3234 -
23d
Wada E.Kanemasa S.Tsuge O. Bull. Chem. Soc. Jpn. 1989, 62: 1198 -
23e
Tsuge O.Hatta T.Yakata K.Maeda H. Chem. Lett. 1994, 1833 -
23f
Tsuge O.Hatta T.Yoshitomi H.Kurosaka K.Fujiwara T.Maeda H.Kakehi A. Heterocycles 1995, 41: 225 -
23g
Tsuge O.Hatta T.Fujiwara T.Yokohari T.Tsuge A. Heterocycles 1999, 50: 661 -
23h
Fallis AG.Parra S.Legoupy S.Woo S. Org. Lett. 1999, 1: 1013 -
23i
Fallis AG.Squire N.Woo S. Org. Lett. 1999, 1: 573 - 24
Spino C.Liu G. J. Org. Chem. 1993, 58: 817 - 25
Spino C.Beaulieu C. J. Am. Chem. Soc. 1998, 120: 11832 - 26
Danishefsky S.Bednarski M. Tetrahedron Lett. 1984, 25: 721 - 27
Spino C.Tu N.Liu G.Girard S. J. Org. Chem. 1994, 59: 5596 -
28a
Reich HJ.Eisenhart EK.Whipple WL.Kelly MJ. J. Am. Chem. Soc. 1988, 110: 6432 ; and references therein -
28b
Spino C.Thibault C.Gingras S. J. Org. Chem. 1998, 63: 5283 - 29
Sieburth SM.Lang J. J. Org. Chem. 1999, 64: 1780 - 30
Dion A.Dubé P.Spino C. Org. Lett. 2005, in press