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DOI: 10.1055/s-0029-1217171
Hydrolytic Kinetic Resolution as an Emerging Tool in the Synthesis of Bioactive Molecules
Publication History
Publication Date:
13 May 2009 (online)
Abstract
A variety of racemic epoxides mainly derived from terminal olefins, such as aliphatic epoxides, multifunctionalized epoxides and amine-substituted epoxides, have been successfully resolved into the enantiomerically pure epoxides and diols using Jacobsen’s hydrolytic kinetic resolution (HKR) method. The chiral epoxides thus prepared were further elaborated by synthetic manipulation to provide a variety of compounds of biological interest. A general synthetic strategy for the construction of syn/anti-1,3-polyol systems using iterative HKR has been developed, which was subsequently utilized in the synthesis of natural products with a broad range of biological activity. The protocol for the 1,3-polyols was also further extended to the synthesis of 1,3-amino alcohols.
1 Introduction
2 Aliphatic/Aromatic Epoxides
2.1 Synthesis of (R)- and (S)-Massoialactone
2.2 Synthesis of Iso-cladospolide B and Cladospolide B
2.3 Synthesis of Herbarumin III
2.4 Synthesis of Decarestrictine D
2.5 Concise Synthesis of (-)-Deoxoprosopinine
2.6 Synthesis of cis-Lauthisan
2.7 Synthesis of CMI-977 (LDP-977)
2.8 Synthesis of (S)-Betaxolol and (S)-Metoprolol
2.9 Synthesis of (S)-Vigabatrin and (S)-Dihydrokavain
3 Multifunctionalized Epoxides
3.1 Synthesis of (+)-Boronolide
4 Amine-Substituted Epoxides
4.1 Synthesis of Protected (2 R,4S )-4-Hydroxyornithine
5 Development of a General Synthetic Strategy for the Construction of 1,3-Polyols
6 Synthesis of Compounds Containing 1,3-Polyols and Amino Alcohols
6.1 Synthesis of Tarchonanthuslactone and Cryptocarya Diacetate
6.2 Synthesis of Strictifolione
6.3 Synthesis of the Lactone Moiety of Compactin
6.4 Synthesis of Verbalactone
6.5 Synthesis of Tetrahydrolipstatin
6.6 Synthesis of Decarestrictine J
6.7 Construction of a 1,3-Amino Alcohol: Application to the Synthesis of (+)-Negamycin
7 Conclusion
Key words
hydrolytic kinetic resolution - terminal epoxides - natural products - synthesis - biological activity
-
1a
Johnson RA.Sharpless KB. Catalytic Asymmetric SynthesisOjima I. VCH; New York: 1993. Chap. 4.1. -
1b
Jacobsen EN. Catalytic Asymmetric SynthesisOjima I. VCH; New York: 1993. Chap. 4.2. - 2
Tokunaga M.Larrow JF.Kakiuchi F.Jacobsen EN. Science (Washington, D.C.) 1997, 277: 936 - 4
Schaus SE.Brandes BD.Larrow JF.Tokunaga M.Hansen KB.Gould AE.Furrow ME.Jacobsen EN. J. Am. Chem. Soc. 2002, 124: 1307 - 5
Kumar P.Naidu SV.Gupta P. Tetrahedron 2007, 63: 2745 -
6a
Abe S. J. Chem. Soc. Jpn. 1937, 58: 246 -
6b
Meijer ThM. Recl. Trav. Chim. Pays-Bas 1940, 59: 191 - 7
Gupta P.Naidu SV.Kumar P. Tetrahedron Lett. 2004, 45: 849 - For reviews on ring-closing metathesis, see:
-
8a
Grubbs RH.Chang S. Tetrahedron 1998, 54: 4413 -
8b
Prunet J. Angew. Chem. Int. Ed. 2003, 42: 2826 - For reviews on cyclic sulfites/cyclic sulfates, see:
-
9a
Lohray BB. Synthesis 1992, 1035 -
9b
Byun H.-S.He L.Bittman R. Tetrahedron 2000, 56: 7051 - 10
Cameron JS.Abbanat D.Bernan VS.Maiese WM.Greenstein M.Jompa J.Ireland CM. J. Nat. Prod. 2000, 63: 142 -
11a
Hirota H.Hirota A.Sakai H.Isogai A.Takahashi T. Bull. Chem. Soc. Jpn. 1985, 58: 2147 -
11b
Hirota A.Sakai H.Isogai A. Agric. Biol. Chem. 1985, 49: 731 -
11c
Fujii Y.Fukuda A.Hamasaki T.Ichimoto I.Nakajima H. Phytochemistry 1995, 40: 1443 - 12
Pandey SK.Kumar P. Tetrahedron Lett. 2005, 46: 6625 -
13a
Becker H.Sharpless KB. Angew. Chem. Int. Ed. 1996, 35: 448 -
13b
Kolb HC.VanNieuwenhze MS.Sharpless KB. Chem. Rev. 1994, 94: 2483 - 14
Inanaga J.Hirata K.Saeki H.Katsuki T.Yamaguchi M. Bull. Chem. Soc. Jpn. 1979, 52: 1989 - 15
Rivero-Cruz JF.Macías M.Cerda-García-Rojas CM.Mata R. J. Nat. Prod. 2003, 66: 511 - 16
Mata R.Macias M.Rojas S.Lotina-Hensen B.Toscano R.Anaya A. Phytochemistry 1998, 49: 441 - 17
Gupta P.Kumar P. Tetrahedron: Asymmetry 2007, 18: 1688 - 18
Gurjar MK.Karmakar S.Mohapatra DK. Tetrahedron Lett. 2004, 45: 4525 -
19a
Grabley S.Granzer E.Hutter K.Ludwig D.Mayer M.Thiericke R.Till G.Wink J.Phillips S.Zeeck A. J. Antibiot. 1992, 45: 56 -
19b
Gohrt A.Zeeck A.Hutter K.Kirsch R.Kluge H.Thiericke R. J. Antibiot. 1992, 45: 66 - 20
Ayer WA.Sun M.Browne LM.Brinen LS.Clardy J. J. Nat. Prod. 1992, 55: 649 - 21
Gupta P.Kumar P. Eur. J. Org. Chem. 2008, 1195 -
22a
Ratle G.Monseur X.Das BC.Yassi J.Khuong-Huu Q.Goutarel R. Bull. Soc. Chim. Fr. 1966, 2945 -
22b
Khuong-Huu Q.Ratle G.Monseur X.Goutarel R. Bull. Soc. Chim. Belg. 1972, 81: 425 -
22c
Khuong-Huu Q.Ratle G.Monseur X.Goutarel R. Bull. Soc. Chim. Belg. 1972, 81: 443 - 23
Staudinger H.Meyer J. Helv. Chim. Acta 1919, 2: 635 - 24
Pandey SK.Kumar P. Synlett 2007, 2894 - For reviews concerning marine natural products, including medium-ring ethers, see:
-
25a
Moore RE. Marine Natural Products Vol. 1:Scheuer PJ. Academic Press; New York: 1978. p.43-121 -
25b
Erickson KL. Marine Natural Products Vol. 5:Scheuer PJ. Academic Press; New York: 1983. p.131-257 -
25c
Blunt JW.Copp BR.Munro MHG.Northcote PT.Prinsep MR. Nat. Prod. Rep. 2005, 22: 15 ; and earlier reviews in the same series - 26
Irie T.Suzuki M.Masamune T. Tetrahedron Lett. 1965, 1091 - For reviews on the Swern oxidation, see:
-
27a
Tidwell TT. Synthesis 1990, 857 -
27b
Tidwell TT. Org. React. 1990, 39: 297 - 28
Tripathi D.Pandey SK.Kumar P. Tetrahedron 2009, 65: 2226 -
29a
Cai X.Cheah S.Chen SM.Eckman J.Ellis J.Fisher R.Fura A.Grewal G.Hussion S.Ip S.Killian DB.Garahan L.-L.Lounsbury H.Qian CG.Scannell RT.Yaeger D.Wypij DM.Yeh CG.Young MA.Yu SX. Abstracts of Papers of the American Chemical Society 1997, 214: 2A-Medi - 30
Gurjar MK.Murugaiah AMS.Radhakrishna P.Ramana CV.Chorghade MS. Tetrahedron: Asymmetry 2003, 14: 1363 -
31a
Reza M.Dion RB. J. Pharm. Pharmaceut. Sci. 2001, 4: 185 -
31b
Bodor N.El-Koussi AA.Kano M.Khalifa MM. J. Med. Chem. 1988, 31: 1651 -
32a
Robinson CP. Drugs Today 1986, 22: 213 -
32b
Morrselli PL,De Santis L, andAdamski R. inventors; US Patent 4,342,783. ; Chem. Abstr. 1982, 97, 168936 -
32c
Teerlink J.Massie B. Am. J. Cardiol. 1999, 84: 94 -
33a
Nathanson JA. J. Pharmacol. Exp. Ther. 1998, 245: 94 -
33b
Johnson G.Forssman O. Cardiovascular Information, β-Blocker and Cardiac ArrhythmiasHassle AB. Molndal; Sweden: 1981. -
33c
Young JW, andBarberich TJ. inventors; US Patent 5,362,757. ; Chem. Abstr. 1992, 117, 258255 -
34a
Berrospi AR.Leibowitz HM. Arch. Ophthalmol. 1982, 100: 943 -
34b
Hussain SS.Aboul-Enein HY.
Al-DhakanHannan M. Toxicology 1989, 12: 77 -
34c
Manoury PMJ,Cavero IAG,Majer H, andGiudicelli PRL. inventors; DE Patent 2649605. ; Chem. Abstr. 1977, 87, 134543 - 35
Muthukrishnan M.Garud D.Joshi RR.Joshi RA. Tetrahedron 2007, 63: 1872 -
36a
Metcalf BW.Casara P. Tetrahedron Lett. 1975, 3337 -
36b
Metcalf BW.Casara P. J. Chem. Soc., Chem. Commun. 1979, 119 -
36c
Casara P. Tetrahedron Lett. 1994, 35: 3049 -
37a
Pittler MH.Ernst E. J. Clin. Psychopharmacol. 2000, 20: 84 -
37b
Smith KK.Dharmaratne HRW.Feltenstein MW.Broom SL.Roach JT.Nanayakkara NPD.Khan IA.Sufka KJ. Psychopharmacology (Berlin) 2001, 155: 86 -
37c
Wu D.Yu L.Nair MG.DeWitt DL.Ramsewak RS. Phytomedicine 2002, 9: 41 - 38
Paul Raj IV.Sudalai A. Tetrahedron Lett. 2008, 49: 2646 -
39a
Davies-Coleman MT.Rivett DEA. Fortschr. Chem. Org. Naturst. 1989, 55: 1 -
39b
Ohloff G. Fortschr. Chem. Org. Naturst. 1978, 35: 431 -
39c
Aditychaudhury N.Das AK. J. Sci. Ind. Res. 1979, 38: 265 -
39d
Siegel SM. Phytochemistry 1976, 15: 566 - 40
Davies-Coleman MT.Rivett DEA. Phytochemistry 1987, 26: 3047 - 41
Watt J.Brandwijk MGB. The Medicinal and Poisonous Plants of Southern and Eastern Africa Livingston; Edinburgh: 1962. p.516 - 42
Kumar P.Naidu SV. J. Org. Chem. 2006, 71: 3935 -
43a
Fujita Y. Bull. Chem. Soc. Jpn. 1959, 32: 439 -
43b
Makisumi S. J. Biochem. (Tokyo) 1961, 49: 284 -
44a
Bell EA.Tirimanna ASL. Nature (London) 1963, 197: 901 -
44b
Bell EA.Tirimanna ASL. Biochem. J. 1964, 91: 356 - 45
Pandey SK.Pandey M.Kumar P. Tetrahedron Lett. 2008, 49: 3297 - 46
Rychnovsky SD. Chem. Rev. 1995, 95: 2021 - 47
Gupta P.Naidu SV.Kumar P. Tetrahedron Lett. 2005, 46: 6571 - 48
Kumar P.Gupta P.Naidu SV. Chem. Eur. J. 2006, 12: 1397 - 49
Juliawaty LD.Kitajima M.Takayama H.Achmad SA.Aimi N. Phytochemistry 2000, 54: 989 - For reviews on cross metathesis, see:
-
50a
Connon SJ.Blechert S. Angew. Chem. Int. Ed. 2003, 42: 1900 ; Angew. Chem. 2003, 115, 1944 -
50b
Gibson SE.Keen SP. Top. Organomet. Chem. 1998, 1: 155 - 52
Goldstein JL.Brown MS. Annu. Rev. Biochem. 1977, 46: 897 - 54
Magiatis P.Spanakis D.Mitaku S.Tsitsa E.Mentis A.Harvala C. J. Nat. Prod. 2001, 64: 1093 - 55
Doshida J.Hasegawa H.Onuki H.Shimidzu N.
J. Antibiot. 1996, 49: 1105 -
57a
Fernández E.Borgström B. Biochim. Biophys. Acta 1989, 1001: 249 -
57b
Fernández E.Borgström B. Lipids 1990, 25: 549 -
57c
Hermier D.Hales P.Brindley DN. FEBS Lett. 1991, 286: 186 -
57d
Hogan S.Fleury A.Hardvary P.Lengfeld H.Meier MK.Triscari J.Sullivan AC. Int. J. Obes. 1987, 11: 35 - 59
Yadav JS.Rao KV.Prasad AR. Synthesis 2006, 3888 - 60
Grabley S.Granzer E.Hütter K.Ludwig D.Mayer M.Thiericke R.Till G.Wink J.Philipps S.Zeeck A.
J. Antibiot. 1992, 45: 56 - 62
Hamada M.Takeuchi T.Kondo S.Ikeda Y.Naganawn H.Maeda K.Olrami Y.Umezawa H. J. Antibiot. 1970, 23: 170 -
63a
Nicolaou KC.Webber SE. Synthesis 1986, 453 -
63b
Takao K.Ochiai H.Yoshida K.Hashizuka T.Koshimura H.Tadano K.Ogawa S. J. Org. Chem. 1995, 60: 8179 - 64
Naidu SV.Kumar P. Tetrahedron Lett. 2007, 48: 3793
References
For information, see: http://www.Rhodiachirex.com.
51Kumar, P.; Naidu, S. V. unpublished results
53Kumar, P.; Naidu, S. V. unpublished results
56Cherian, S. K.; Naidu, S. V.; Kumar, P. unpublished results.
58Tripathi, D.; Kumar, P. unpublished work.
61Choudhary, P. S.; Gupta, P.; Kumar, P. unpublished work.