A guide to IUPAC nomenclature of organic compounds: recommendations 1993 ; (including revisions, published and hitherto unpublished, to the 1979 edition of Nomenclature of organic chemistry)
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| Format: | Book |
| Language: | English |
| Published: |
Oxford u.a.
Blackwell
1993
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| Subjects: | |
| Online Access: | Inhaltsverzeichnis |
| Item Description: | Frühere Ausg. u.d.T.: Nomenclature of organic chemistry |
| Physical Description: | XV, 190 S. zahlr. graph. Darst. |
| ISBN: | 0632034882 |
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| 110 | 2 | |a International Union of Pure and Applied Chemistry |b Commission on the Nomenclature of Organic Chemistry |e Verfasser |0 (DE-588)1034740-9 |4 aut | |
| 245 | 1 | 0 | |a A guide to IUPAC nomenclature of organic compounds |b recommendations 1993 ; (including revisions, published and hitherto unpublished, to the 1979 edition of Nomenclature of organic chemistry) |c International Union of Pure and Applied Chemistry, Organic Chemistry Division, Commission on Nomenclature of Organic Chemistry (III.1). Prepared for publ. by R. Panico ... |
| 246 | 1 | 3 | |a IUPAC nomenclature of organic compounds |
| 246 | 1 | 3 | |a Nomenclature of organic compounds |
| 264 | 1 | |a Oxford u.a. |b Blackwell |c 1993 | |
| 300 | |a XV, 190 S. |b zahlr. graph. Darst. | ||
| 336 | |b txt |2 rdacontent | ||
| 337 | |b n |2 rdamedia | ||
| 338 | |b nc |2 rdacarrier | ||
| 500 | |a Frühere Ausg. u.d.T.: Nomenclature of organic chemistry | ||
| 650 | 4 | |a Chemistry, Organic |x Nomenclature | |
| 650 | 0 | 7 | |a Nomenklatur |0 (DE-588)4126152-5 |2 gnd |9 rswk-swf |
| 650 | 0 | 7 | |a Organische Verbindungen |0 (DE-588)4043816-8 |2 gnd |9 rswk-swf |
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| 689 | 0 | 1 | |a Nomenklatur |0 (DE-588)4126152-5 |D s |
| 689 | 0 | |5 DE-604 | |
| 700 | 1 | |a Panico, Robert |e Sonstige |4 oth | |
| 856 | 4 | 2 | |m Digitalisierung TU Muenchen |q application/pdf |u http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=005991753&sequence=000002&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA |3 Inhaltsverzeichnis |
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| adam_text | Contents
Membership of the Commission during the Preparation of this Guide,
xi
List of Tables,
xii
Preamble,
xiii
R-0 INTRODUCTION,
1
R-0.0 Scope,
1
R-0.1 Conventions,
1
R-0.
1.1
Spelling,
1
R-0.
1.2
Position of locants,
1
R-0.1.3 Punctuation,
2
R-0.
1.3.1
Commas,
2
R-0.1.3.2 Full stops,
2
R-0.
1.3.3
Colons,
2
R-0.1.3.4 Hyphens,
2
R-0.1.3.5 Spaces,
3
R-0.
1.4
Numerical (multiplicative) prefixes,
4
R-0.
1.5
Enclosing marks,
5
R-0.1.5.1 Parentheses,
5
R-0.
1.5.2
Square brackets,
6
R-O.1.5.3
Braces,
7
R-0.
1.6
Italicization,
7
R-0.
1.6.1
Lower case italic letters,
8
R-0.
1.6.2
Italicized element symbols,
8
R-0.1.6.3
Italic words, syllables and capital
roman
letters,
8
R-0.
1.7
Elision and addition of vowels,
8
R-0.1.8 Order of prefixes,
10
R-0.2 Glossary,
13
R-0.2.1 Parent structures,
13
R-0.2.
1.1
Parent hydride,
13
R-0.2.
1.2
Functional parent,
13
R-0.2.2 Groups,
13
R-0.2.2.1
Substituem
atom or group,
13
R-0.2.2.2 Characteristic group,
13
R-O.2.2.3 Principal group,
13
R-O.2.3 Names,
14
R-0.2.3.1 Trivial name,
14
R-O.2.3.2 Semisystematic name or semitrivial name,
14
R-0.2.3.3 IUPAC name,
14
R-O.2.3.3.1 Fusion name,
14
R-0.2.3.3.2 Hantzsch-Widman name,
14
R-0.2.3.3.3 Functional class name,
14
R-0.2.3.3.4 Radicofunctional name,
15
R-0.2.3.3.5 Replacement name,
15
R-0.2.3.3.6
Substitutive
name,
15
CONTENTS
R-O.2.3.3.7
Conjunctive
name,
15
R-O.2.3.3.8 Additive
name,
16
R-0.2.3.3.9 Subtractive
name,
16
R-0.2.3.3.10
Multiplicative name,
17
R-0.2.4
Other terms used in these recommendations,
17
R-0.2.4.1 Seniority, senior,
17
R-0.2.4.2 Lowest set of locants,
17
R-l GENERAL PRINCIPLES OF ORGANIC NOMENCLATURE,
18
R-1.0 Introduction,
18
R-
1.1
Bonding number,
20
R-l.
1.1
Definitional
R-l.
1.2
Standard bonding numbers,
21
R-l.
1.3
Nonstandard
bonding numbers,
21
R-l.
1.4
Contiguous formal double bonds,
21
R-l.
2
Nomenclature operations,
22
R-l.2.1
Substitutive
operation,
22
R-l.
2.2
Replacement operation,
23
R-l.2.3 Additive operation,
24
R-l.
2.3.1
By use of an additive prefix,
24
R-l.2.3.2 By use of an additive suffix,
25
R-l.2.3.
3
By use of a separate word,
25
R-l
.2.3.4
By connecting the names of the components of an addition compound with a dash (long hyphen),
26
R-l.2.3.5 By juxtaposition or multiplication of
substituent
prefix terms,
26
R-l.
2.4
Conjunctive operation,
26
R-l.
2.4.1
By juxtaposition of component names,
26
R-l.
2.4.2
By placing a multiplicative prefix before the name of the corresponding parent hydride,
27
R-l.
2.5
Subtractive operation,
27
R-l.
2.5.1
By use of a prefix,
28
R-l.
2.5.2
By a change in ending or addition of a suffix,
29
R-l.
2.6
Ring formation or cleavage,
30
R-
1.2.6.1
The prefix cyclo-,
30
R-l.
2.6.2
The prefix
seco-,
31
R-l.2.7 Rearrangement,
31
R-l.2.7.1 The prefix abeo-,
31
R-l.
2.7.2
The prefix retro-,
32
R-l.
2.8
Multiplicative operation,
32
R-1.3 Indicated hydrogen,
34
R-2 PARENT HYDRIDES AND THEIR DERIVED
SUBSTITUENT
GROUPS,
36
R-2.0 Introduction,
36
R-2.1 Mononuclear hydrides,
36
R-2.2 Acyclic polynuclear hydrides,
36
R-2.2.1 Hydrocarbons,
36
R-2.2.2 Homogeneous hydrides other than hydrocarbons or boron hydrides,
37
R-2.2.3 Heterogeneous hydrides,
38
R-2.3 Monocyclic hydrides,
39
R-2.3.1 Hydrocarbons,
39
R-2.3.2 Homogeneous hydrides other than hydrocarbons or boron hydrides,
39
R-2.3.3 Heterogeneous hydrides other than heteropolyboron hydrides,
40
R-2.4 Polycyclic parent hydrides,
44
R-2.4.1 Fusion nomenclature,
44
R-2.4.2 Bridged parent hydrides
-
extension of the
von
Baeyer system,
49
R-2.4.2.
1
Bicyclic ring systems,
49
vi
CONTENTS
R-2.4.2.2
R-2.4.3
R-2.4.3.1
R-2.4.3.2
R-2.4.3.3
R-2.4.4
R-2.4.4.1
R-2.4.4.2
R-2.4.5
R-2.4.6
R-2.5
R-3
R-3.0
R-3.
R-3.
R-3 1
1.3
1.4
R-3.1
R-3.1
R-3.2
R-3.2.1
R-3.2.2
R-3.3
R-3.4
R-4
R-4.0
R-4.1
R-4.2
R-5
R-5.0
R-5.1
R-5.1.1
R-5.1.2
R-5.1.3
R-5.1.4
R-5.1.4.1
R-5.1.4.2
R-5.2
R-5.2.1
R-5.2.2
R-5.2.3
R-5.3
R-5.3.1
R-5.3.2
R-5.3.3
R-5.3.3.0
R-5.3.3.1
R-5.3.3.2
R-5.3.3.3
R-5.3.3.4
R-5.3.3.5
R-5.3.4
R-5.3.5
Polycyclic
ring systems,
50
Spiro
parent hydrides,
51
Monospiro
parent hydrides,
51
Polyspiro parent hydrides,
52
Spiro
parent hydrides containing polycyclic ring systems,
53
Ring assemblies,
53
Assemblies of two identical cyclic systems,
53
Unbranched assemblies consisting of three or more identical ring systems,
54
Cyclophanes,
55
Natural product parent hydrides,
55
Substituent
prefix names derived from parent hydrides,
56
CHARACTERISTIC (FUNCTIONAL) GROUPS,
59
Introduction,
59
Unsaturation,
59
Suffixes denoting multiple bonds,
59
Hydro prefixes,
60
Dehydro prefixes,
61
Substituent
prefix names for unsaturated/saturated parent hydrides,
62
Specification of characteristic groups,
62
Prefixes and suffixes,
62
Functional modifiers,
64
Functional parent compounds and derived
substituent
groups,
65
Functional replacement,
66
GUIDE TO NAME CONSTRUCTION,
68
Introduction,
68
General principles,
68
Examples,
72
APPLICATIONS TO SPECIFIC CLASSES OF COMPOUNDS,
77
Introduction,
77
Binary hydrides and related parent hydrides,
77
Hydrocarbons,
77
Chalcogen hydrides,
78
Hydrides of the group
15
elements,
78
Silicon parent hydrides,
79
Silanes,
79
Heterogeneous silicon hydrides: siloxanes and analogues,
79
Organometallic compounds,
81
Organometallic compounds of antimony, bismuth, germanium, tin, and lead,
81
Organometallic compounds in which the metal is bound only to carbon atoms of organic groups and
hydrogen,
81
Organometallic compounds with
anionie ligands,
82
Halogen,
nitro, nitroso,
azo,
diazo
and azido compounds,
82
Halogen compounds,
82
Nitro
and
nitroso
compounds,
83
Azo,
azoxy, diazo, and related compounds,
83
Diazenes,
83
Azo
compounds,
84
Azoxy compounds,
85
Diazonium compounds,
86
Azo
compounds with the general structure
R
N=N X,
86
Diazo compounds,
87
Azides.
87
Isodiazenes.
87
CONTENTS
R-5.4
Amines and ¡mines,
87
R-5.4.1 Primary amines,
88
R-5.4.2 Secondary and tertiary amines,
88
R-5.4.3 Imines,
89
R-5.4.4 Hydroxylamines,
90
R-5.4.5
Amine
oxides,
90
R-5.5 Hydroxy compounds, their derivatives and analogues,
91
R-5.5.1 Hydroxy compounds and analogues,
91
R-5.5.1.1 Alcohols and phenols,
91
R-5.5.1.2 Sulfur, selenium, and tellurium analogues of alcohols and phenols,
92
R-5.5.2
Substituent
prefixes derived from alcohols, phenols, and their analogues,
93
R-5.5.3 Salts,
94
R-5.5.4 Ethers and chalcogen analogues,
94
R-5.5.4.1
Substitutive
names,
94
R-5.5.4.2 Functional class names,
95
R-5.5.4.3 Replacement nomenclature,
95
R-5.5.4.4 Cyclic ethers,
95
R-5.5.5
Hydroperoxides
and peroxides,
96
R-5.5.6 Hydropolysulfides and polysulfides,
97
R-5.5.7 Sulfoxides, sulfones, and their analogues,
97
R-5.6 Aldehydes, ketones, their derivatives and analogues,
98
R-5.6.1 Aldehydes, thioaldehydes, and their analogues,
98
R-5.6.2 Ketones, thioketones, and their analogues,
100
R-5.6.2.1 Ketones,
100
R-5.6.2.2 Chalcogen analogues of ketones,
101
R-5.6.3 Ketenes,
101
R-5.6.4
Acetáis, hemiacetals,
acylals, and their analogues,
102
R-5.6.4.1
Acetáis,
102
R-5.6.4.2 Hemiacetals,
103
R-5.6.4.3 Acylals,
103
R-5.6.5 Acyloins,
104
R-5.6.6 Nitrogenous derivatives of carbonyl compounds,
104
R-5.6.6.1 Oximes,
104
R-5.6.6.2 Hydrazones,
105
R-5.6.6.3 Azines,
105
R-S.ć.ó^
Other nitrogen derivatives of carbonyl compounds,
105
R-5.7 Adds and related characteristic groups,
106
R-5.7.1 Carboxylic acids,
107
R-5.7.1.1 Simple (unsubstituted) acyclic mono- and dicarboxylic acids,
107
R-5.7.1.2 Substituted carboxylic acids,
109
R-5.7.1.2.1 Hydroxy, alkoxy, and
охо
acids,
109
R-5.7.
1.2.2
Amic
and anilic acids,
109
R-5.7.1.2.3
Amino
acids,
110
R-5.7.1.3 Modification of carboxylic acid suffixes,
110
R-5.7.1.3.1 Peroxy acids,
110
R-5.7.1.
3.2
Imidic, hydrazonic, and hydroximic acids,
110
R-5.7.1.3.3 Hydroxamic acids,
112
R-5.7.
1.3.4
Thiocarboxylic and thiocarbonic acids,
112
R-5.7.2
Chalcogen acids containing chalcogen atoms directly linked to an organic group,
113
R-5.7.2.
1
Sulfur acids containing sulfur atoms directly linked to an organic group,
113
R-5.7.2.2 Selenium acids containing selenium directly linked to an organic group,
115
R-5.7.3 Phosphorus and arsenic acids containing phosphorus or arsenic atoms directly linked to an organic
group,
115
R-5.7.3.1 Phosphorus
охо
acids and replacement modifications,
115
R-5.7.3.2 Arsenic
охо
acids and replacement modifications,
116
R-5.7.4 Salts and esters,
117
VIII
CONTENTS
R-5.7.4.1
Salts,
117
R-5.7.4.2 Esters,
117
R-5.7.5 Lactones, lactams, lactims, and analogues,
119
К-бЛ.ЗЛ
Lactones,
120
R-5.7.5.2 Sultones,
120
R-5.7.5.3 Lactams and lactims,
121
R-5.7.5.4 Sultams,
121
R-5.7.6 Acid halides,
122
R-5.7.7 Anhydrides and their analogues,
123
R-5.7.7.1 Symmetrical anhydrides,
123
R-5.
7.7.2
Unsymmetrical (mixed) anhydrides,
124
R-5.
7.7.3
Chalcogen analogues of anhydrides,
124
R-5.
7.8
Amides, imides, and hydrazides,
125
R-5.
7.8.1
Monoacyl derivatives of ammonia (primary amides),
125
R-5.7.8.2 Symmetrical diacyl and triacyl derivatives of ammonia,
127
R-5.7.8.3 Imides,
128
R-5.7.8.4 Hydrazides,
128
R-5.7.9 Nitriles, isocyanides and related compounds,
129
R-5.7.9.1 Nitriles,
129
R-5.7.9.2 Cyanide-related compounds,
131
R-5.7.9.3 Nitrile oxides,
131
R-5.8 Radicals and ions,
132
R-5.8.1 Radicals,
132
R-5.8.1.1
Monovalent
radicals,
132
R-5.8.
1.2
Divalent and trivalent radicals,
132
R-5.8.1.
3
Radical centres on characteristic groups,
134
R-5.8.2 Cations,
136
R-5.8.3 Anions,
139
R-5.8.4 Cationic and
anionie
centres in a single structure,
141
R-5.8.5 Radical ions,
141
R-6 NAME INTERPRETATION,
143
R-6.0 Introduction,
143
R-6.1 6-(4-Hydroxyhex-l-en-l-yl)undeca-2,4-diene-7,9-diyne-l,l 1-diol,
143
R-6.2 2,3-Dichloro-6-[4-chloro-2-(hydroxymethyl)-5-oxohex-3-en-l-yl]pyridine-4-carboxylic acid,
144
R-6.3 3-(2,3-Dihydroxypropyl)-a-methylquinoline-2-pentanoic acid,
145
R-6.4 4,4 -Dinitro-2,3 -[ethylenebis(sulfanediyl)]dicyclohexane-l-carbaldehyde,
146
R-6.5 1-Methylbutyl 4-(2-acetyl-2-ethylhydrazino)benzoate,
147
R-7 STEREOCHEMICAL SPECIFICATION,
149
R-7.0 Introduction,
149
R-7.1 cis-trans Isomerism
-
the E/Z convention,
149
R-7.
1.0
Introduction,
149
R-7.
1.1
cis
and trans Isomers,
149
R-7.
1.2
The E/Z convention,
151
R-7.
2
Chiral compounds
-
specification of absolute configuration,
152
R-7.2.1 The R/S convention,
152
R-7.2.2 Relative configuration,
154
R-8 ISOTOPICALLY MODIFIED COMPOUNDS,
155
R-8.0 Introduction,
155
R-8.1 Symbols and definitions,
155
R-8.1.1 Nuclide symbols,
155
R-8.
1.2
Atomic symbols,
155
R-8.
1.3
Isotopically unmodified compounds,
156
R-8.
1.4
Isotopically modified compounds,
156
CONTENTS
R-8.2 Isotopically
substituted compounds,
156
R-8.2.1
Formulae,
156
R-8.2.2
Names,
157
R-8.3 Isotopically
labelled compounds,
157
R-8.3.1
Specifically labelled compounds,
157
R-8.3.2 Selectively labelled compounds,
158
R-8.3.
3
Nonselectively labelled compounds,
160
R-8.3.4 Isotopically deficient compounds,
160
R-9 APPENDIX,
162
R-9.0 Introduction,
162
R-9.1 Trivial and semisystematic names retained for naming organic compounds,
162
R-9.2 Bridge names,
180
R-9.2.1 Simple bivalent bridges,
180
R-9.2.2 Simple polyvalent bridges,
182
R-9.3 V Prefixes used in replacement nomenclature,
182
INDEX,
183
|
| any_adam_object | 1 |
| author_corporate | International Union of Pure and Applied Chemistry Commission on the Nomenclature of Organic Chemistry |
| author_corporate_role | aut |
| author_facet | International Union of Pure and Applied Chemistry Commission on the Nomenclature of Organic Chemistry |
| author_sort | International Union of Pure and Applied Chemistry Commission on the Nomenclature of Organic Chemistry |
| building | Verbundindex |
| bvnumber | BV009052180 |
| callnumber-first | Q - Science |
| callnumber-label | QD291 |
| callnumber-raw | QD291 |
| callnumber-search | QD291 |
| callnumber-sort | QD 3291 |
| callnumber-subject | QD - Chemistry |
| classification_rvk | VK 5030 |
| classification_tum | CHE 601b |
| ctrlnum | (OCoLC)59883711 (DE-599)BVBBV009052180 |
| dewey-full | 547.0014 |
| dewey-hundreds | 500 - Natural sciences and mathematics |
| dewey-ones | 547 - Organic chemistry |
| dewey-raw | 547.0014 |
| dewey-search | 547.0014 |
| dewey-sort | 3547.0014 |
| dewey-tens | 540 - Chemistry and allied sciences |
| discipline | Chemie / Pharmazie Chemie |
| format | Book |
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| genre | (DE-588)1071861417 Konferenzschrift gnd-content |
| genre_facet | Konferenzschrift |
| id | DE-604.BV009052180 |
| illustrated | Illustrated |
| indexdate | 2024-07-09T17:29:18Z |
| institution | BVB |
| institution_GND | (DE-588)1034740-9 |
| isbn | 0632034882 |
| language | English |
| oai_aleph_id | oai:aleph.bib-bvb.de:BVB01-005991753 |
| oclc_num | 59883711 |
| open_access_boolean | |
| owner | DE-355 DE-BY-UBR DE-91G DE-BY-TUM DE-703 DE-19 DE-BY-UBM DE-11 DE-188 |
| owner_facet | DE-355 DE-BY-UBR DE-91G DE-BY-TUM DE-703 DE-19 DE-BY-UBM DE-11 DE-188 |
| physical | XV, 190 S. zahlr. graph. Darst. |
| publishDate | 1993 |
| publishDateSearch | 1993 |
| publishDateSort | 1993 |
| publisher | Blackwell |
| record_format | marc |
| spelling | International Union of Pure and Applied Chemistry Commission on the Nomenclature of Organic Chemistry Verfasser (DE-588)1034740-9 aut A guide to IUPAC nomenclature of organic compounds recommendations 1993 ; (including revisions, published and hitherto unpublished, to the 1979 edition of Nomenclature of organic chemistry) International Union of Pure and Applied Chemistry, Organic Chemistry Division, Commission on Nomenclature of Organic Chemistry (III.1). Prepared for publ. by R. Panico ... IUPAC nomenclature of organic compounds Nomenclature of organic compounds Oxford u.a. Blackwell 1993 XV, 190 S. zahlr. graph. Darst. txt rdacontent n rdamedia nc rdacarrier Frühere Ausg. u.d.T.: Nomenclature of organic chemistry Chemistry, Organic Nomenclature Nomenklatur (DE-588)4126152-5 gnd rswk-swf Organische Verbindungen (DE-588)4043816-8 gnd rswk-swf (DE-588)1071861417 Konferenzschrift gnd-content Organische Verbindungen (DE-588)4043816-8 s Nomenklatur (DE-588)4126152-5 s DE-604 Panico, Robert Sonstige oth Digitalisierung TU Muenchen application/pdf http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=005991753&sequence=000002&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA Inhaltsverzeichnis |
| spellingShingle | A guide to IUPAC nomenclature of organic compounds recommendations 1993 ; (including revisions, published and hitherto unpublished, to the 1979 edition of Nomenclature of organic chemistry) Chemistry, Organic Nomenclature Nomenklatur (DE-588)4126152-5 gnd Organische Verbindungen (DE-588)4043816-8 gnd |
| subject_GND | (DE-588)4126152-5 (DE-588)4043816-8 (DE-588)1071861417 |
| title | A guide to IUPAC nomenclature of organic compounds recommendations 1993 ; (including revisions, published and hitherto unpublished, to the 1979 edition of Nomenclature of organic chemistry) |
| title_alt | IUPAC nomenclature of organic compounds Nomenclature of organic compounds |
| title_auth | A guide to IUPAC nomenclature of organic compounds recommendations 1993 ; (including revisions, published and hitherto unpublished, to the 1979 edition of Nomenclature of organic chemistry) |
| title_exact_search | A guide to IUPAC nomenclature of organic compounds recommendations 1993 ; (including revisions, published and hitherto unpublished, to the 1979 edition of Nomenclature of organic chemistry) |
| title_full | A guide to IUPAC nomenclature of organic compounds recommendations 1993 ; (including revisions, published and hitherto unpublished, to the 1979 edition of Nomenclature of organic chemistry) International Union of Pure and Applied Chemistry, Organic Chemistry Division, Commission on Nomenclature of Organic Chemistry (III.1). Prepared for publ. by R. Panico ... |
| title_fullStr | A guide to IUPAC nomenclature of organic compounds recommendations 1993 ; (including revisions, published and hitherto unpublished, to the 1979 edition of Nomenclature of organic chemistry) International Union of Pure and Applied Chemistry, Organic Chemistry Division, Commission on Nomenclature of Organic Chemistry (III.1). Prepared for publ. by R. Panico ... |
| title_full_unstemmed | A guide to IUPAC nomenclature of organic compounds recommendations 1993 ; (including revisions, published and hitherto unpublished, to the 1979 edition of Nomenclature of organic chemistry) International Union of Pure and Applied Chemistry, Organic Chemistry Division, Commission on Nomenclature of Organic Chemistry (III.1). Prepared for publ. by R. Panico ... |
| title_short | A guide to IUPAC nomenclature of organic compounds |
| title_sort | a guide to iupac nomenclature of organic compounds recommendations 1993 including revisions published and hitherto unpublished to the 1979 edition of nomenclature of organic chemistry |
| title_sub | recommendations 1993 ; (including revisions, published and hitherto unpublished, to the 1979 edition of Nomenclature of organic chemistry) |
| topic | Chemistry, Organic Nomenclature Nomenklatur (DE-588)4126152-5 gnd Organische Verbindungen (DE-588)4043816-8 gnd |
| topic_facet | Chemistry, Organic Nomenclature Nomenklatur Organische Verbindungen Konferenzschrift |
| url | http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=005991753&sequence=000002&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA |
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