-
4
-
-
33744738548
-
-
For an example of carbonylation of a similar indole see: A.B. Smith III, L. Kürti, and A.H. Davulcu Org. Lett. 8 2006 2167 2170
-
(2006)
Org. Lett.
, vol.8
, pp. 2167-2170
-
-
Kürti, L.1
Davulcu, A.H.2
-
5
-
-
49349132015
-
-
For example: Y. Tamura, T. Kawasaki, M. Adachi, M. Tanio, and Y. Kita Tetrahedron Lett. 18 1977 4417 4420
-
(1977)
Tetrahedron Lett.
, vol.18
, pp. 4417-4420
-
-
Tamura, Y.1
Kawasaki, T.2
Adachi, M.3
Tanio, M.4
Kita, Y.5
-
9
-
-
33846061736
-
-
T. Dohi, K. Morimoto, N. Takenaga, A. Goto, A. Maruyama, Y. Kiyono, H. Tohma, and Y. Kita J. Org. Chem. 72 2007 109 116
-
(2007)
J. Org. Chem.
, vol.72
, pp. 109-116
-
-
Dohi, T.1
Morimoto, K.2
Takenaga, N.3
Goto, A.4
Maruyama, A.5
Kiyono, Y.6
Tohma, H.7
Kita, Y.8
-
10
-
-
79957592922
-
Chlorosulfonyl Isocyanate
-
M.J. Miller, M. Ghosh, P.R. Guzzo, P.F. Vogt, J. Hu, G.F. Filzen, and A.G. Geyer Chlorosulfonyl Isocyanate D. Crich, A.B. Charette, P.L. Fuchs, G. Molander, L.A. Paquette, Encyclopedia of Reagents for Organic Synthesis (Online) 2010 Wiley & Sons New York
-
(2010)
Encyclopedia of Reagents for Organic Synthesis (Online)
-
-
Miller, M.J.1
Ghosh, M.2
Guzzo, P.R.3
Vogt, P.F.4
Hu, J.5
Filzen, G.F.6
Geyer, A.G.7
-
13
-
-
79957614901
-
-
The yield of 10 is based on the NMR purity of a crude weight
-
The yield of 10 is based on the NMR purity of a crude weight.
-
-
-
-
14
-
-
0001286881
-
-
G. Lohaus Chem. Ber. 100 1967 2719 2729
-
(1967)
Chem. Ber.
, vol.100
, pp. 2719-2729
-
-
Lohaus, G.1
-
17
-
-
0141741411
-
-
We found only one example in which a carboxamide was directly introduced at C-7 of an indole, accomplished by directed ortho metallation. See: C.G. Hartung, A. Fecher, B. Chapell, and V. Snieckus Org. Lett. 5 2003 1899 1902
-
(2003)
Org. Lett.
, vol.5
, pp. 1899-1902
-
-
Hartung, C.G.1
Fecher, A.2
Chapell, B.3
Snieckus, V.4
-
18
-
-
79957598691
-
-
German Patent DE 1010958, June 27
-
Graf, R. Carboxylic amides. German Patent DE 1010958, June 27, 1957.
-
(1957)
Carboxylic Amides
-
-
Graf, R.1
-
20
-
-
79957591370
-
-
In some of our previous cyanations with CSI we had noticed two minor byproducts, one corresponding to the indole-3-carboxamide, and another which appeared to result from a second addition of CSI to the indole
-
In some of our previous cyanations with CSI we had noticed two minor byproducts, one corresponding to the indole-3-carboxamide, and another which appeared to result from a second addition of CSI to the indole.
-
-
-
-
21
-
-
79957591140
-
-
The identity of 15 was confirmed by NMR
-
The identity of 15 was confirmed by NMR.
-
-
-
-
24
-
-
25844520463
-
-
A.W. Jones, T.D. Wahyuningsih, K. Pchalek, N. Kumar, and D.S.C. Black Tetrahedron 61 2005 10490 10500
-
(2005)
Tetrahedron
, vol.61
, pp. 10490-10500
-
-
Jones, A.W.1
Wahyuningsih, T.D.2
Pchalek, K.3
Kumar, N.4
Black, D.S.C.5
-
25
-
-
0001052366
-
-
For example: S. Nakatsuka, T. Masuda, O. Asano, T. Teramae, and T. Goto Tetrahedron Lett. 27 1986 4327 4330
-
(1986)
Tetrahedron Lett.
, vol.27
, pp. 4327-4330
-
-
Nakatsuka, S.1
Masuda, T.2
Asano, O.3
Teramae, T.4
Goto, T.5
-
27
-
-
0033935493
-
-
S.S. Nakkady, M.M. Fathy, O.H. Hishmat, S.S. Mahmond, and M.Y. Ebeid Boll. Chim. Farm. 139 2000 59 66
-
(2000)
Boll. Chim. Farm.
, vol.139
, pp. 59-66
-
-
Nakkady, S.S.1
Fathy, M.M.2
Hishmat, O.H.3
Mahmond, S.S.4
Ebeid, M.Y.5
-
28
-
-
0028070649
-
-
For example: D.S.C. Black, M.C. Bowyer, M.M. Catalano, A.J. Ivory, P.A. Keller, N. Kumar, and S.J. Nugent Tetrahedron 50 1994 10497 10508
-
(1994)
Tetrahedron
, vol.50
, pp. 10497-10508
-
-
Black, D.S.C.1
Bowyer, M.C.2
Catalano, M.M.3
Ivory, A.J.4
Keller, P.A.5
Kumar, N.6
Nugent, S.J.7
-
30
-
-
79957595736
-
-
note
-
2O: C, 59.17; H, 3.58; N, 20.70. Found: C, 58.97; H, 3.37; N, 20.50.
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-
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