Backes / Bellus / Drayton Index Volume Category 6

1. Auflage 2013
ISBN: 978-3-13-178591-6
Verlag: Thieme
Format: PDF
Kopierschutz: Adobe DRM (»Systemvoraussetzungen)

E-Book, Englisch, 1000 Seiten, PDF, Format (B × H): 170 mm x 255 mm

Reihe: Science of Synthesis

Science of Synthesis provides a critical review of the synthetic methodology developed from the early 1800s to date for the entire field of organic and organometallic chemistry. As the only resource providing full-text descriptions of organic transformations and synthetic methods as well as experimental procedures, Science of Synthesis is therefore a unique chemical information tool.Over 1000 world-renowned experts have chosen the most important molecular transformations for a class of organic compounds and elaborated on their scope and limitations. The systematic, logical and consistent organization of the synthetic methods for each functional group enables users to quickly find out which methods are useful for a particular synthesis and which are not. Effective and practical experimental procedures can be implemented quickly and easily in the lab.The content of this e-book was originally published in December 2009.

Zielgruppe

Wissenschaftler

Autoren/Hrsg.

Bellus, D.

Noyori, R.

Regitz, M.

Schaumann, E.

Shinkai, I.

Backes, Jutta

Drayton, Colin J.

Fachgebiete

• Naturwissenschaften Chemie Organische Chemie

Inhaltsverzeichnis

1;Science of Synthesis: Category 6 Cumulative Index – Compounds with All-Carbon Functions;1
1.1;Imprint;5
1.2;Title page;6
1.3;List of All Volumes;7
1.4;Preface;12
1.5;Table of Contents;14
1.6;Product Class Overview;16
1.7;Structure Index;28
1.7.1;Compounds with All-Carbon Functions: Monocyclic Compounds;28
1.7.2;Compounds with All-Carbon Functions: Bicyclic Compounds;63
1.7.3;Compounds with All-Carbon Functions: Tricyclic Compounds;98
1.7.4;Compounds with All-Carbon Functions: Tetracyclic Compounds;134
1.7.5;Compounds with All-Carbon Functions: Pentacyclic Compounds;160
1.7.6;Compounds with All-Carbon Functions: Hexacyclic Compounds;179
1.7.7;Compounds with All-Carbon Functions: Heptacyclic Compounds;188
1.7.8;Compounds with All-Carbon Functions: Octacyclic Compounds;203
1.7.9;Compounds with All-Carbon Functions: Nonacyclic Compounds;208
1.7.10;Compounds with All-Carbon Functions: Decacyclic Compounds;213
1.7.11;Compounds with All-Carbon Functions: Undecacyclic Compounds;216
1.7.12;Compounds with All-Carbon Functions: Dodecacyclic Compounds;219
1.7.13;Compounds with All-Carbon Functions: Tridecacyclic Compounds;220
1.7.14;Compounds with All-Carbon Functions: Pentadecacyclic Compounds;224
1.7.15;Compounds with All-Carbon Functions: Hexadecacyclic Compounds;225
1.7.16;Compounds with All-Carbon Functions: Heptadecacyclic Compounds;226
1.7.17;Compounds with All-Carbon Functions: Tricosacyclic Compounds (23);227
1.7.18;Compounds with All-Carbon Functions: Heptacosacyclic Compounds (27);228
1.7.19;Compounds with All-Carbon Functions: Nonacosacyclic Compounds (29);229
1.7.20;Compounds with All-Carbon Functions: Polycyclic Compounds;230
1.8;Name Reaction Index;232
1.8.1;A;232
1.8.2;B;232
1.8.3;C;233
1.8.4;D;234
1.8.5;E;235
1.8.6;F;236
1.8.7;G;236
1.8.8;H;237
1.8.9;I;238
1.8.10;J;238
1.8.11;K;239
1.8.12;L;239
1.8.13;M;239
1.8.14;N;241
1.8.15;O;241
1.8.16;P;241
1.8.17;Q;242
1.8.18;R;242
1.8.19;S;242
1.8.20;T;244
1.8.21;U;244
1.8.22;V;244
1.8.23;W;244
1.8.24;Y;245
1.8.25;Z;245
1.9;Keyword Index;246
1.9.1;A;246
1.9.2;B;326
1.9.3;C;361
1.9.4;D;415
1.9.5;E;439
1.9.6;F;452
1.9.7;G;456
1.9.8;H;459
1.9.9;I;469
1.9.10;J;475
1.9.11;K;476
1.9.12;L;481
1.9.13;M;483
1.9.14;N;488
1.9.15;O;497
1.9.16;P;502
1.9.17;Q;530
1.9.18;R;531
1.9.19;S;534
1.9.20;T;547
1.9.21;U;559
1.9.22;V;560
1.9.23;W;561
1.9.24;X;561
1.9.25;Y;562
1.9.26;Z;562
1.10;Author Index;564
1.10.1;A;564
1.10.2;B;571
1.10.3;C;589
1.10.4;D;603
1.10.5;E;612
1.10.6;F;616
1.10.7;G;624
1.10.8;H;635
1.10.9;I;650
1.10.10;J;654
1.10.11;K;658
1.10.12;L;675
1.10.13;M;687
1.10.14;N;707
1.10.15;O;715
1.10.16;P;721
1.10.17;Q;731
1.10.18;R;731
1.10.19;S;741
1.10.20;T;764
1.10.21;U;775
1.10.22;V;777
1.10.23;W;782
1.10.24;X;792
1.10.25;Y;793
1.10.26;Z;798
1.11;Erratum;802
1.12;Abbreviations;804
1.13;List of All Volumes;810

Leseproben

Structure Index

This index comprises a list of key cyclic substructures present in the products of Category 6 (Compounds with All-Carbon Functions).

To use this index you first need to identify the following four characteristics for the ring system you are interested in:

1. whether the system is monocyclic, bicyclic, etc. (see page header)
2. the ring size, i.e. three membered, four membered, etc. (see left-hand column)
3. the number of heteroatoms within the ring system (see left-hand column)
4. heteroatoms are prioritized in the following order:
   1. main-group elements: (O, S, Se, Te, N, P, As, Sb, Bi)
   2. main-group metals: (Si, Ge, Sn, Pb, B, Al, Ga, In, Tl, Mg)
   3. transition, lanthanide, and actinide metals

Having identified the ring system of interest, please refer to the number beneath the structure in order to determine the relevant volume number (small and bold) and page number within the...