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Volumn 86, Issue 1, 1986, Pages 35-67

Syntheses of 2, 3, 6-Trideoxy-3-amino- and 2, 3, 6-Trideoxy-3-nitrohexoses

Author keywords

[No Author keywords available]

Indexed keywords


EID: 33845375960     PISSN: 00092665     EISSN: 15206890     Source Type: Journal    
DOI: 10.1021/cr00071a003     Document Type: Article
Times cited : (168)

References (269)
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    • DiMarco, A.1    Arcamone, F.2    Zunino, F.3
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    • (1978) , vol.2 , pp. 89-229
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    • (1978) , vol.15 , pp. 125-164
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    • (1979) , vol.1 , pp. 2
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    • Cancer Chemotherapy
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    • “Rules of Carbohydrate Chemistry”. Report by the Division of Carbohydrate Chemistry of the American Chemical Society under the chairmanship of Dr. M. L. Wolfrom and a British Committee on Carbohydrate Nomenclature. The report was approved by the Committee of Nomenclature, Spelling and Pronunciation of the American Chemical Society and by the Council of the American Chemical Society in March 1962. J. Org. Chem. 1963, 28, 281.
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    • Bn and Bz have been used as abbreviations for benzyl and benzoate
    • respectively. Less well-known abbreviations used for reagents: BnSH, benzyl mercaptan; DBU, 1, 8-diazabicy-clo[5.4.0]undec-7-ene; DEAD, diethyl azodicarboxylate; DIBAL, diisobutylaluminum hydride; DMAP, 4-(dimethyl-amino)pyridine; NIS, N-iodosuccinimide; NMO, N-methyl-morpholine N-oxide; PCC, pyridinium chlorochromate; PDC, pyridinium dichromate; Py, pyridine; TFAA, trifluoroacetic anhydride; TMNO, trimethylamine N-oxide
    • Bn and Bz have been used as abbreviations for benzyl and benzoate, respectively. Less well-known abbreviations used for reagents: BnSH, benzyl mercaptan; DBU, 1, 8-diazabicy-clo[5.4.0]undec-7-ene; DEAD, diethyl azodicarboxylate; DIBAL, diisobutylaluminum hydride; DMAP, 4-(dimethyl-amino)pyridine; NIS, N-iodosuccinimide; NMO, N-methyl-morpholine N-oxide; PCC, pyridinium chlorochromate; PDC, pyridinium dichromate; Py, pyridine; TFAA, trifluoroacetic anhydride; TMNO, trimethylamine N-oxide.
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    • Except for the protecting group on the C-4 hydroxyl moiety
    • or the synthesis of 4-epi-vancosamine (6). These authors reported that reaction of 56 with alkaline cyanide gave a product with theribo configuration
    • or the synthesis of 4-epi-vancosamine (6). These authors reported that reaction of 56 with alkaline cyanide gave a product with the ribo configuration.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.