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For the original isolation of palau'amine and its related congener, see: a, Sceptrin
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0033524887
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Axinellamine
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0141518579
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Massadine:, For recent synthetic studies of palau'amine and/or its related congener, see
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4143115664
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For the method developed by Al-Mourabit and co-workers that was used to prepare 13, see: a
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69
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77955208578
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-
The stereochemistry at C10 in 19 was confirmed by the conversion of the intermediate into phakellins and comparison of the optical rotation of the synthetic material to that of the natural product
-
The stereochemistry at C10 in 19 was confirmed by the conversion of the intermediate into phakellins and comparison of the optical rotation of the synthetic material to that of the natural product. The stereochemistry at C6 in 19 was inferred based upon the reasoning depicted in Scheme 5.
-
The Stereochemistry at C6 in 19 Was Inferred Based Upon the Reasoning Depicted in Scheme 5
-
-
-
70
-
-
77955189977
-
-
No optical rotation was observed for 20
-
No optical rotation was observed for 20.
-
-
-
-
71
-
-
77955187344
-
-
The stereochemistry of 17b was confirmed by using X-ray diffraction analysis. See the Supporting Information
-
The stereochemistry of 17b was confirmed by using X-ray diffraction analysis. See the Supporting Information.
-
-
-
-
72
-
-
77955217970
-
-
The stereochemistry at C6 in 22 was determined using NOE analysis of 28 Supporting Information
-
The stereochemistry at C6 in 22 was determined using NOE analysis of 28 (Supporting Information).
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-
-
-
73
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-
77955196653
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-
A similar cyclization approach for the synthesis of phakellstatins has been described by Romo and his co-workers. However, in their case, only decomposition of the starting urea was observed
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A similar cyclization approach for the synthesis of phakellstatins has been described by Romo and his co-workers. However, in their case, only decomposition of the starting urea was observed.
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-
-
-
74
-
-
0031013358
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-
O. Kitagawa, M. Fujita, H. Li, T. Taguchi, Tetrahedron Lett. 1997, 38, 615-618.
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(1997)
Tetrahedron. Lett.
, vol.38
, pp. 615-618
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-
Kitagawa, O.1
Fujita, M.2
Li, H.3
Taguchi, T.4
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