Synthesis of Polyfluorinated and Polychlorinated Hydrocarbons
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1 Synthesis of Polyfluorinated and Polychlorinated Hydrocarbons Yong Guan Feb. 13, 2009 Nicoletti, M.; O Hagan, D.; Slawin, A.M.Z. J. Am. Chem. Soc. 2005, 127, 482. Hunter, L.; O Hagan, D.; Slawin, A.M.Z. J. Am. Chem. Soc. 2006, 128, Hunter, L.; Slawin, A. M. Z.; Kirsch, P.; O Hagan, D. Angew. Chem., Int. Ed. 2007, 46, Shibuya, G. M., Kanady, J. S., Vanderwal, C. D. J. Am. Chem. Soc. 2008, 130, Yoshimitsu, T., Fukumoto, N., Tanaka, T. J. Org. Chem. 2009, 74, 696. Nilewski, C., Geisser, R. W.; Erick M. Carreira. Nature 2009, 457, 573.
2 Outline Synthesis of Polyfluorinated Hydrocarbons Synthesis of Polychlorinated Hydrocarbons
3 Outline Synthesis of Polyfluorinated Hydrocarbons Synthesis of Polychlorinated Hydrocarbons
4 α,β,γ-trifluoroalkanes Nicoletti, M.; O Hagan, D.; Slawin, A.M.Z. J. Am. Chem. Soc. 2005, 127, 482.
5 α,β,γ-trifluoroalkanes a R = C 5 H 11, R = CH 3, b R = C 7 H 15, R = C 5 H 10 Ph. (i) mcpba in DCM, 0 C, 2 h. (ii) HF pyridine in DCM, 10 C, 4 h. (iii,iv) SOCl 2, py. in DCM, 0 C, 45 min then NaIO 4 / RuCl 3 in CH 3 CN/H 2 O, 0 C 1 h. (v) TBAF in acetone, 0 C 2 h. (vi) Et 2 O/H 2 SO 4. (vii) Tf 2 O, pyr in DCM, -40 C, 1 h. (viii) TBAF in MeCN, 0 C, 30 min. Nicoletti, M.; O Hagan, D.; Slawin, A.M.Z. J. Am. Chem. Soc. 2005, 127, 482.
6 α,β,γ-trifluoroalkanes a R = C 5 H 11, R = CH 3, b R = C 7 H 15, R = C 5 H 10 Ph. (i) mcpba in DCM, 0 C, 2 h. (ii) HF pyridine in DCM, 10 C, 4 h. (iii,iv) SOCl 2, py. in DCM, 0 C, 45 min then NaIO 4 / RuCl 3 in CH 3 CN/H 2 O, 0 C 1 h. (v) TBAF in acetone, 0 C 2 h. (vi) Et 2 O/H 2 SO 4. (vii) Tf 2 O, pyr in DCM, -40 C, 1 h. (viii) TBAF in MeCN, 0 C, 30 min. Nicoletti, M.; O Hagan, D.; Slawin, A.M.Z. J. Am. Chem. Soc. 2005, 127, 482.
7 α,β,γ-trifluoroalkanes a R = C 5 H 11, R = CH 3, b R = C 7 H 15, R = C 5 H 10 Ph. (i) mcpba in DCM, 0 C, 2 h. (ii) HF pyridine in DCM, 10 C, 4 h. (iii,iv) SOCl 2, py. in DCM, 0 C, 45 min then NaIO 4 / RuCl 3 in CH 3 CN/H 2 O, 0 C 1 h. (v) TBAF in acetone, 0 C 2 h. (vi) Et 2 O/H 2 SO 4. (vii) Tf 2 O, pyr in DCM, -40 C, 1 h. (viii) TBAF in MeCN, 0 C, 30 min. Nicoletti, M.; O Hagan, D.; Slawin, A.M.Z. J. Am. Chem. Soc. 2005, 127, 482.
8 α,β,γ-trifluoroalkanes Nicoletti, M.; O Hagan, D.; Slawin, A.M.Z. J. Am. Chem. Soc. 2005, 127, 482.
9 α,β,γ-trifluoroalkanes F F OH vicinal C F bonds preferring to align gauche to each other Nicoletti, M.; O Hagan, D.; Slawin, A.M.Z. J. Am. Chem. Soc. 2005, 127, 482.
10 All-syn Four Vicinal Fluorine Motif Hunter, L.; O Hagan, D.; Slawin, A.M.Z. J. Am. Chem. Soc. 2006, 128,
11 All-syn Four Vicinal Fluorine Motif (a) Et 3 N 3HF, Na 2 SO 4, 70 C; (b) BnBr, NaH, DMF, 40 C; (c) Grubbs second generation catalyst, DCM, Δ; (d) KMnO 4, MgSO 4, EtOH, H 2 O, -10 C; (e) SOCl 2, pyridine, DCM, 0 C; (f) NaIO 4, RuCl 3, MeCN, H 2 O, 0 C; (g) TBAF, MeCN, rt; (h) H 2 SO 4, H 2 O, THF, rt. Hunter, L.; O Hagan, D.; Slawin, A.M.Z. J. Am. Chem. Soc. 2006, 128,
12 All-syn Four Vicinal Fluorine Motif (a) Tf 2 O, pyridine, DCM, -40 C; (b) TBAF, MeCN, 0 C; (c) Deoxo-Fluor, 70 C; (d) H 2, Pd/C, MeOH, rt; (e) TsCl, 2,4,6-collidine, 50 C. Hunter, L.; O Hagan, D.; Slawin, A.M.Z. J. Am. Chem. Soc. 2006, 128,
13 All-syn Four Vicinal Fluorine Motif C2 symmetry; Dihedral angles of 66.7 (F9-C-C-F10) and 59.7 (F10-C-C-F10 ) between vicinal fluorines; The aryl and fluoroalkyl groups pack in separate domains; Intermolecular interactions include a hydrogen bond (2.52 Å) from the fluorine atom of C10 (and C10 ) to the hydrogen atom at C9 (and C9 ) of an adjacent molecule. Hunter, L.; O Hagan, D.; Slawin, A.M.Z. J. Am. Chem. Soc. 2006, 128,
14 α,β,γ,δ-tetrafluoroalkane Hunter, L.; Slawin, A. M. Z.; Kirsch, P.; O Hagan, D. Angew. Chem., Int. Ed. 2007, 46, 7887.
15 α,β,γ,δ-tetrafluoroalkane a) Grubbs 2nd-generation catalyst, DCM, Δ; b) KMnO 4, MgSO 4, EtOH, DCM, H 2 O, 0 C; c) SOCl 2, pyridine, DCM, rt; d) NaIO 4, RuCl 3, MeCN, H 2 O, rt; e) Bu 4 NF, MeCN, rt; f) H 2 SO 4, H 2 O, THF, RT; g) H 2, Pd/C, MeOH, rt; h) TsCl, collidine, 50 C; i) Deoxo-Fluor, DCM, Δ. Hunter, L.; Slawin, A. M. Z.; Kirsch, P.; O Hagan, D. Angew. Chem., Int. Ed. 2007, 46, 7887.
16 α,β,γ,δ-tetrafluoroalkane a) Grubbs 2nd-generation catalyst, DCM, Δ; b) KMnO 4, MgSO 4, EtOH, DCM, H 2 O, 0 C; c) SOCl 2, pyridine, DCM, rt; d) NaIO 4, RuCl 3, MeCN, H 2 O, rt; e) Bu 4 NF, MeCN, rt; f) H 2 SO 4, H 2 O, THF, RT; g) H 2, Pd/C, MeOH, rt; h) TsCl, collidine, 50 C; i) Deoxo-Fluor, DCM, Δ. Hunter, L.; Slawin, A. M. Z.; Kirsch, P.; O Hagan, D. Angew. Chem., Int. Ed. 2007, 46, 7887.
17 α,β,γ,δ-tetrafluoroalkane Left: The simplified model system 6. Middle: Calculated linear conformations and right: either minimum (6a, 6c) or next higher energy conformation (6b). C gray, F green, H white; red arrows indicate g + g - -F F interactions. Relative energies are in kcal mol -1. 1) g + g - -F F interaction costs about 3.4 kcal mol -1 in steric strain 2) 1,3-F CH3 interaction costs 4.04 kcal mol -1 3) vicinal fluorine gauche effect (ca. 0.8 kcal mol -1 ) has only a secondary influence Hunter, L.; Slawin, A. M. Z.; Kirsch, P.; O Hagan, D. Angew. Chem., Int. Ed. 2007, 46, 7887.
18 Outline Synthesis of Polyfluorinated Hydrocarbons Synthesis of Polychlorinated Hydrocarbons
19 Dichlorination of Allylic Alcohol Derivatives Unnamed chlorosulfolipids isolated from Adriatic mussels (1-3) and from freshwater algae (4) and algae-derived protein kinase inhibitor malhamensilipin A (5) Gerwick, W. H., et al. J. Nat. Prod. 1994, 57, 524 Ciminiello, P., et al. J. Org. Chem. 2001, 66, 578 Ciminiello, P., et al. J. Am. Chem. Soc. 2002, 124,
20 Dichlorination of Allylic Alcohol Derivatives Probable conforma9onal preference of chlorosulfolipid 1. g = gauche, a = an9. Shibuya, G. M., Kanady, J. S., Vanderwal, C. D. J. Am. Chem. Soc. 2008, 130,
21 Dichlorination of Allylic Alcohol Derivatives Markó-Maguire Reagents R R 1 or BnNEt 3, KMnO 4, Me 3 SiCl R R 1 R R Cl Cl Cl Cl R 1 R 1 R, R1 = Alkyl, Ary, H 60-95% yield Markó, I. E.; Richardson, P. R.; Bailey, M.; Maguire, A. R.; Coughlan,N. Tetrahedron Lett. 1997, 38, 2339.
22 Dichlorination of Allylic Alcohol Derivatives Mioskowski Reagents RCCl 2 CHO RCH 2 CHO RCOCHClR RCOCH 2 R RCOCClRCOOR' RCOCHR'COOR' RCCl=CClR' R R' Et 4 N + (Cl 3 ) - RCH=CHR' RCHClCHClR' R Cl O O R H O O PhOR p-clc 6 H 4 OR Schlama, T.; Gabriel, K.; Gouverneur, V.; Mioskowski, C. Angew. Chem., Int. Ed. 1997, 36, 2341.
23 Dichlorination of Allylic Alcohol Derivatives Comparison of the Markó-Maguire and Mioskowski Reagents for Diastereoselective Vicinal Dichlorination of Allylic Alcohol Derivatives (TBS = tert- Butyldimethylsilyl, Piv = Pivaloate) Shibuya, G. M., Kanady, J. S., Vanderwal, C. D. J. Am. Chem. Soc. 2008, 130,
24 Dichlorination of Allylic Alcohol Derivatives Shibuya, G. M., Kanady, J. S., Vanderwal, C. D. J. Am. Chem. Soc. 2008, 130,
25 Dichlorination of Allylic Alcohol Derivatives Shibuya, G. M., Kanady, J. S., Vanderwal, C. D. J. Am. Chem. Soc. 2008, 130,
26 Dichlorination of Allylic Alcohol Derivatives Diastereoselective Synthesis of a Stereotetrad Relevant to Chlorosulfolipid 1 Shibuya, G. M., Kanady, J. S., Vanderwal, C. D. J. Am. Chem. Soc. 2008, 130,
27 Dichlorination of Allylic Alcohol Derivatives Synthesis of Pyran 16 to Confirm the Relative Stereochemistry of Dichlorination Shibuya, G. M., Kanady, J. S., Vanderwal, C. D. J. Am. Chem. Soc. 2008, 130,
28 Nucleophilic Multiple Chlorination Yoshimitsu, T., Fukumoto, N., Tanaka, T. J. Org. Chem. 2009, 74, 696.
29 Nucleophilic Multiple Chlorination Yoshimitsu, T., Fukumoto, N., Tanaka, T. J. Org. Chem. 2009, 74, 696.
30 Nucleophilic Multiple Chlorination Yoshimitsu, T., Fukumoto, N., Tanaka, T. J. Org. Chem. 2009, 74, 696.
31 Nucleophilic Multiple Chlorination All reactions were carried out using NCS (3 equiv) and PPh 3 (3 equiv) in toluene
32 Nucleophilic Multiple Chlorination Rationale for Configurational Retention at the C3 Position Yoshimitsu, T., Fukumoto, N., Tanaka, T. J. Org. Chem. 2009, 74, 696.
33 Nucleophilic Multiple Chlorination All reactions were carried out using NCS (3 equiv) and PPh 3 (3 equiv) in toluene at 90 C
34 Nucleophilic Multiple Chlorination Yoshimitsu, T., Fukumoto, N., Tanaka, T. J. Org. Chem. 2009, 74, 696.
35 Nucleophilic Multiple Chlorination a The reaction was carried out using NCS (3 equiv) and Ph 2 PCl (2 equiv) in CH 2 Cl 2 at rt. b Racemic substrate was used. c The reaction was carried out using NCS (3 equiv) and Ph2PCl (3 equiv) in CH 2 Cl 2 at rt.
36 Nucleophilic Multiple Chlorination Tetrachlorination of Bisepoxides 4n-q with NCS/Ph 3 P Yoshimitsu, T., Fukumoto, N., Tanaka, T. J. Org. Chem. 2009, 74, 696.
37 Total synthesis of a chlorosulpholipid Nilewski, C., Geisser, R. W.; Erick M. Carreira. Nature 2009, 457, 573.
38 Total synthesis of a chlorosulpholipid (a) (H 5 C 2 ) 4 NCl 3, CH 2 Cl 2, 0 C, 45 min, 68%; (b) DIBAL (2.3 equiv.), H 5 C 2 H 5 C 6, 0 C, 10 min, 72%; (c) imidazole (1.5 equiv.), t-bu(h 3 C) 2 SiCl (1.2 equiv.), CH 2 Cl 2, 0 C to room temperature (RT, 20 C), 30 min, 87%; (d) OsO 4 (5 mol%),nmo(1.1 equiv.), acetone/h 2 O, RT, 19 h, 68%; (e) DABCO (3.0 equiv.), (F 3 CSO 2 ) 2 O (1.0 equiv.), -78 C, 10 min, then diol, -78 C to RT, 15 h, 75% (96% based on recovered starting material); (f) (1)-CSA (0.1 equiv.), CH 3 OH, RT, 3 h, 98%; (g) (COCl) 2 (1.3 equiv.), (H 3 C) 2 SO (2.5 equiv.), CH 2 Cl 2, -78 C, 10 min, then 10 (1.0 equiv.), -78 C, 30 min, then (H 5 C 2 ) 3 N (5.4 equiv.), -78 C to RT, 1h; (h) 11 (1.05 equiv.), n-buli (1.05 equiv.), THF, -78 C, then RT, 10 min, followed by aldehyde (1.0 equiv.) at -78 C, 5 min, then RT, 30 min, 62% over two steps; (i) (H 3 C) 3 SiCl (2.0 equiv.), CH 2 Cl 2, H 3 CCO 2 C 2 H 5, 11.5 h, 39% 15, 4%16, 10% mixture of S N 2 products (31% starting material recovered);
39 Total synthesis of a chlorosulpholipid anchimeric participation of chlorides (j) (H 5 C 2 ) 4 NCl 3 (3.0 equiv.), CH 2 Cl 2, 0 C, 10 min, 51%; (k) (+)-CSA (10 mol%), CH 3 OH, 12 h, 80%; (l) DAIB (1.1 equiv.), TEMPO (0.1 equiv.), CH 2 Cl 2, RT, 16.5 h; (m) CrCl 2 (6.9 equiv.), CHCl 3 (2.6 equiv.), THF, 65 C, 49% over two steps; (n) SO 3 -pyridine (6.0 equiv.), THF, 30 min, 27% (66% starting material recovered). Nilewski, C., Geisser, R. W.; Erick M. Carreira. Nature 2009, 457, 573.
40 Total synthesis of a chlorosulpholipid (a) m-cpba, CH 2 Cl 2, 0 C to RT, d.r.=1:1, 95% overall; (b) 4Å molecular sieves, NMO (1.1 equiv.), TPAP (5 mol%), CH 2 Cl 2, 6h; 11 (1.6 equiv.), n-buli (1.6 equiv.), THF, -78 C, RT, 10 min; then addition of the aldehyde solution to the phosphonium ylide at -78 C, 1 h, then RT, 1.5 h, 34% (56% based on recovered starting material); (c) (H 3 C) 3 SiCl (2.0 equiv.), CH 2 Cl 2, H 3 CCO 2 C 2 H 5, 9 h, 43% (73% based on recovered starting material); (d) (H 5 C 2 ) 4 NCl 3 (3.0 equiv.), CH 2 Cl 2, -78 C, 2 h, d.r.=10:1, 93% overall; (e) (+)-CSA (10 mol%), CH 3 OH, 12 h, 98%; Nilewski, C., Geisser, R. W.; Erick M. Carreira. Nature 2009, 457, 573.
41 Total synthesis of a chlorosulpholipid (e) (+)-CSA (10 mol%), CH 3 OH, 12 h, 98%; (f) DAIB (1.3 equiv.), TEMPO (0.2 equiv.), CH 2 Cl 2, RT, 16.5 h; (g) CrCl 2 (6.8 equiv.), CHCl 3 (2.5 equiv.), THF, 65 uc, 47% over two steps; (h) SO 3 - pyridine (3.0 equiv.), THF, 20 min, 99%. Nilewski, C., Geisser, R. W.; Erick M. Carreira. Nature 2009, 457, 573.
42 Conclusions Polyflurinated and polychlorinated compounds have newly gained synthetic interests. Enantio- and stereoselective methods are needed.
43
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