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Buu-Hoi N. P.
BUU-HOI NG. PH.
BUU-HOÏ N. P.
BUU-HOÏ NG. PH.
Buu-Hoi Ng. Ph.
Buu-Hoi N
BUU-HOÏ NG.PH.
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http://hub.abes.fr/acs/periodical/jmcmar/1971/volume_14/issue_11/101021jm00293a006/authorship/5
http://hub.abes.fr/acs/periodical/joceah/1949/volume_14/issue_5/101021jo01157a013/authorship/1
http://hub.abes.fr/acs/periodical/joceah/1950/volume_15/issue_5/101021jo01151a005/authorship/1
http://hub.abes.fr/acs/periodical/joceah/1955/volume_20/issue_7/101021jo01125a003/authorship/1
http://hub.abes.fr/acs/periodical/joceah/1956/volume_21/issue_6/101021jo01112a007/authorship/1
http://hub.abes.fr/acs/periodical/joceah/1956/volume_21/issue_1/101021jo01107a031/authorship/1
http://hub.abes.fr/acs/periodical/jmcmar/1961/volume_3/issue_2/101021jm50015a014/authorship/2
http://hub.abes.fr/acs/periodical/joceah/1951/volume_16/issue_12/101021jo50006a017/authorship/1
http://hub.abes.fr/acs/periodical/joceah/1950/volume_15/issue_5/101021jo01151a007/authorship/1
http://hub.abes.fr/acs/periodical/joceah/1951/volume_16/issue_8/101021jo50002a023/authorship/1
http://hub.abes.fr/acs/periodical/joceah/1951/volume_16/issue_2/101021jo01142a022/authorship/1
http://hub.abes.fr/acs/periodical/joceah/1954/volume_19/issue_8/101021jo01373a021/authorship/1
http://hub.abes.fr/acs/periodical/joceah/1958/volume_23/issue_4/101021jo01098a010/authorship/1
http://hub.abes.fr/acs/periodical/joceah/1959/volume_24/issue_3/101021jo01085a025/authorship/2
http://hub.abes.fr/acs/periodical/joceah/1950/volume_15/issue_1/101021jo01147a021/authorship/1
http://hub.abes.fr/acs/periodical/joceah/1954/volume_19/issue_11/101021jo01376a009/authorship/1
http://hub.abes.fr/acs/periodical/joceah/1957/volume_22/issue_1/101021jo01352a020/authorship/2
http://hub.abes.fr/acs/periodical/joceah/1951/volume_16/issue_8/101021jo50002a004/authorship/1
http://hub.abes.fr/acs/periodical/joceah/1950/volume_15/issue_1/101021jo01147a020/authorship/1
http://hub.abes.fr/acs/periodical/joceah/1953/volume_18/issue_9/101021jo50015a019/authorship/1
http://hub.abes.fr/acs/periodical/joceah/1959/volume_24/issue_1/101021jo01083a618/authorship/1
http://hub.abes.fr/acs/periodical/joceah/1949/volume_14/issue_3/101021jo01155a024/authorship/1
http://hub.abes.fr/acs/periodical/joceah/1951/volume_16/issue_2/101021jo01142a023/authorship/1
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Basic Esters and Hydrazides Derived from Substituted Pyrrylbenzoic Acids
CARCINOGENIC DERIVATIVES OF CARBAZOLE. I. THE SYNTHESIS OF 1,2,7,8-, 1,2,5,6-, AND 3,4,5,6-DIBENZOCARBAZOLE AND SOME OF THEIR DERIVATIVES1
COMPOUNDS WITH POTENTIAL ACTIVITY AGAINST LETHAL RADIATIONS. II.1 POLYPHENOLIC KETONES AND INDOLES DERIVED FROM HIGHER FATTY ACIDS
The Pfitzinger Reaction with Ketones Derived from o-Hydroxydiphenyl
POTENTIAL NITROGEN-HETEROCYCLE CARCINOGENS. IV. SYNTHESIS OF 2,3-BENZOCARBAZOLES AND OF INDENOINDOLES1
Some Nitrogen Derivatives of 1-Fluoronaphthalene
Notes. Synthesis of 2,3-Cyclopenteno-7H-benzo[c]fluorene
Some 2,3-Polymethylene-indoles and -quinolines. An Attempt to Synthesize Large-Ring Nitrogen Heterocycles
POTENTIAL NITROGEN-HETEROCYCLE CARCINOGENS. IX. HALOGEN-CONTAINING ANGULAR BENZO- AND DIBENZO-CARBAZOLES, AND THEIR THIOPHENE ANALOGS
Potential Nitrogen-Heterocycle Carcinogens. XII. 9-Ethylcarbazole-3-Aldehyde and its Derivatives
Aldehydes Derived from 1,2,5-Trisubstituted Pyrroles
2-ARYLPYRROCOLINES AND 2-ARYLPYRIMIDAZOLES
CARCINOGENIC DERIVATIVES OF CARBAZOLE. II. ISOSTERIC COMPOUNDS OF CARBAZOLE CONTAINING A THIOPHENE NUCLEUS1
POTENTIAL NITROGEN-HETEROCYCLE CARCINOGENS. X. CARBAZOLES WITH ACENAPHTHENE AND CYCLOPENTA[a]PHENANTHRENE NUCLEI
The Pfitzinger Reaction in the Synthesis of Quinoline Derivatives
6-Amino derivatives of stigmastanol and cholestanol
POTENTIAL NITROGEN-HETEROCYCLE CARCINOGENS. VI. POLY-SUBSTITUTED 1,2-BENZOCARBAZOLES, 1,2,5,6- AND 1,2,7,8-DIBENZOCARBAZOLES1
POTENTIAL NITROGEN-HETEROCYCLE CARCINOGENS. III. NEW DERIVATIVES OF N-ETHYLCARBAZOLE1
Potential Nitrogen-Heterocycle Carcinogens. XI. Substitution Reactions of N-Alkylcarbazoles
Arylation of Esters of Erucic Acid
Additions and Corrections - Potential Nitrogen-Heterocycle Carcinogens. VI.
COMPOUNDS WITH POTENTIAL ACTIVITY AGAINST LETHAL RADIATIONS. IV.1 KETONES DERIVED FROM α- AND β-NAPHTHOL. A REVISION OF THE LITERATURE
POTENTIAL NITROGEN-HETEROCYCLE CARCINOGENS. VIII. POLYCYCLIC CARBAZOLES WITH PHENOLIC GROUPS1
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