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In this paper, the numbering of the positions in all the synthetic compounds is the same as that in the natural chlorophylls and does not follow the IUPAC-IUB nomenclature to avoid any confusion for readers (see also ref 3).
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In this paper, the numbering of the positions in all the synthetic compounds is the same as that in the natural chlorophylls and does not follow the IUPAC-IUB nomenclature to avoid any confusion for readers (see also ref 3).
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4
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33845599945
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10
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(e) Chen, Y.; Medforth, C. J.; Smith, K. M.; Alderfer, J.; Dougherty, T. J.; Pandey, R. K. J. Org. Chem. 2001, 66, 3930-3939.
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Kimura, S.2
Kimura, T.3
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0038288829
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(a) Li, G.; Dobhal, M. P.; Graham, A.; Shibata, M.; Zheng, G.; Kozyrev, A.; Pandey, R. K. J. Org. Chem. 2003, 68, 3762-3772.
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Li, G.1
Dobhal, M.P.2
Graham, A.3
Shibata, M.4
Zheng, G.5
Kozyrev, A.6
Pandey, R.K.7
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(b) Tamiaki, H.; Omoda, M.; Saga, Y.; Morishita, H. Tetrahedron 2003, 59, 4337-4350.
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Morishita, H.4
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Kunieda, M.1
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Tamiaki, H.3
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20
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34548740765
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cis-Dihydroxychlorins 3 and 5 had two chiral centers on C2/3 and C12/13, respectively, and were racemates.
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cis-Dihydroxychlorins 3 and 5 had two chiral centers on C2/3 and C12/13, respectively, and were racemates.
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22
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0031233216
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Senge, M. O.; Smith, K. M. Acta Crystallogr., C 1997, C53, 1314-1318.
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Acta Crystallogr., C
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Senge, M.O.1
Smith, K.M.2
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24
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34548741291
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1-epimeric mixtures, respectively.
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1-epimeric mixtures, respectively.
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