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4
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0000725865
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Scott, W.J.; Crisp, G.T.; Stille, J.K.; J. Am. Chem. Soc. 1984, 106, 4630. Ritter, K.; Synthesis, 1993, 735. and references therein.
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Scott, W.J.1
Crisp, G.T.2
Stille, J.K.3
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5
-
-
0027180141
-
-
and references therein
-
Scott, W.J.; Crisp, G.T.; Stille, J.K.; J. Am. Chem. Soc. 1984, 106, 4630. Ritter, K.; Synthesis, 1993, 735. and references therein.
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(1993)
Synthesis
, pp. 735
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Ritter, K.1
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7
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85027877554
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Comins, D.L.; Dehghani, A.; Foti, C.J.; Joseph, S.P.; Org. Synth., 1996, 74, 77.
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Comins, D.L.1
Dehghani, A.2
Foti, C.J.3
Joseph, S.P.4
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8
-
-
0013562702
-
-
note
-
Compound 22 will undergo polymerization upon standing at 25°C for more than 1.5 hours, but has excellent room temperature stability when stored as a solution.
-
-
-
-
9
-
-
0013590790
-
-
note
-
We typically notice 10-15% of the aromatization byproduct PhOTf (see Ref 5).
-
-
-
-
10
-
-
0028227540
-
-
Jacobsen, E.N.; Deng, L; Furukawa, Y.; Martinez, L.E.; Tetrahedron, 1994, 50, 4323.
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Tetrahedron
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Jacobsen, E.N.1
Deng, L.2
Furukawa, Y.3
Martinez, L.E.4
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11
-
-
0013563071
-
-
note
-
We have unambiguously established the absolute stereochemistry of the analogous sulfone product and will present the stereochemistry of the triflate products in a subsequent full paper.
-
-
-
-
12
-
-
0000458209
-
-
Such directable reactions include cyclopropanation, dihydroxylation, aminohydroxylation, nucleophilic additions etc.
-
Such directable reactions include cyclopropanation, dihydroxylation, aminohydroxylation, nucleophilic additions etc. see Hoveyda, A.H.; Evans, D.A.; Fu, G.C. Chem. Rev. 1993, 93, 1307.
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Chem. Rev.
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Hoveyda, A.H.1
Evans, D.A.2
Fu, G.C.3
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13
-
-
0028555376
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-
We believe this is the sole literature example which involves any chemistry Pd(0 coupling of an epoxyvinyl triflate
-
M. Y. Chu-Moyer; S. J. Danishefsky; G. K. Schulte J. Am. Chem. Soc. 1994, 116, 11213. We believe this is the sole literature example which involves any chemistry (Pd(0) coupling) of an epoxyvinyl triflate.
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J. Am. Chem. Soc.
, vol.116
, pp. 11213
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-
Chu-Moyer, M.Y.1
Danishefsky, S.J.2
Schulte, G.K.3
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14
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-
0001585871
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(a) Wender, P. A.; Erhardt, J. M.; Letendre, L. J. J. Am. Chem. Soc. 1981, 103, 2114-2116;
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Wender, P.A.1
Erhardt, J.M.2
Letendre, L.J.3
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19
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0000725865
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Scott, W.J.; Crisp, G.T.; Stille, J.K.; J. Am. Chem. Soc. 1984, 106, 4630.
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J. Am. Chem. Soc.
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Scott, W.J.1
Crisp, G.T.2
Stille, J.K.3
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21
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0032546132
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Kulasegaram, S.; Kulawiec, R.J.; Tetrahedron, 1998, 54, 1361. Minami, T.; Hanaoka, M.; Tetrahedron Lett.; 1994, 35, 9425. Suzuki, M.; Oda, Y.; Noyori, R.; J. Am. Chem. Soc. 1979, 101, 1623.
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Kulasegaram, S.1
Kulawiec, R.J.2
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22
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0028102561
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Kulasegaram, S.; Kulawiec, R.J.; Tetrahedron, 1998, 54, 1361. Minami, T.; Hanaoka, M.; Tetrahedron Lett.; 1994, 35, 9425. Suzuki, M.; Oda, Y.; Noyori, R.; J. Am. Chem. Soc. 1979, 101, 1623.
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Minami, T.1
Hanaoka, M.2
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23
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0000743544
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-
Kulasegaram, S.; Kulawiec, R.J.; Tetrahedron, 1998, 54, 1361. Minami, T.; Hanaoka, M.; Tetrahedron Lett.; 1994, 35, 9425. Suzuki, M.; Oda, Y.; Noyori, R.; J. Am. Chem. Soc. 1979, 101, 1623.
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Suzuki, M.1
Oda, Y.2
Noyori, R.3
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24
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0002429680
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Farina, V.; Pure & Appl. Chem. 1996, 68, 73. Farina, V.; Krishnan, B.; J. Am Chem. Soc. 1991, 113, 9585.
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Farina, V.1
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25
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0000131734
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Farina, V.; Pure & Appl. Chem. 1996, 68, 73. Farina, V.; Krishnan, B.; J. Am Chem. Soc. 1991, 113, 9585.
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Farina, V.1
Krishnan, B.2
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26
-
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0013591434
-
-
note
-
Regio and stereochemistry confirmed by hydrogenation of the methylated product in the presence of platinum oxide to provide isomers of methylcyclohexanol which were compared with commercial samples.
-
-
-
-
28
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0000085691
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(b) Johnson, C. R. Acc. Chem. Res. 1998, 31, 333., Johnson, C. R.; Golebiowski, A.; Steensma, D. H. J. Am. Chem. Soc. 1992, 114, 9414.
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Johnson, C.R.1
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0001372934
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Johnson, C.R.1
Golebiowski, A.2
Steensma, D.H.3
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