Backes / Bellus / Drayton | Index Volume Category 3 | E-Book | sack.de
E-Book

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

Reihe: Science of Synthesis

Backes / Bellus / Drayton Index Volume Category 3


1. Auflage 2013
ISBN: 978-3-13-178531-2
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

ISBN: 978-3-13-178531-2
Verlag: Thieme
Format: PDF
 Kopierschutz: Adobe DRM (»Systemvoraussetzungen)

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 May 2008.

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Zielgruppe

Wissenschaftler

Autoren/Hrsg.

Bellus, D.
Noyori, R.
Regitz, M.
Schaumann, E.
Shinkai, I.
Backes, Jutta
Drayton, Colin J.

Fachgebiete

Weitere Infos & Material

1;Science of Synthesis: Category 3 Cumulative Index – Compounds with Four and Three Carbon–Heteroatom Bonds;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;36
1.7.1;Carbonic or Carboxylic Acid Derivatives: Monocyclic Compounds;36
1.7.2;Carbonic or Carboxylic Acid Derivatives: Bicyclic Compounds;76
1.7.3;Carbonic or Carboxylic Acid Derivatives: Tricyclic Compounds;118
1.7.4;Carbonic or Carboxylic Acid Derivatives: Tetracyclic Compounds;145
1.7.5;Carbonic or Carboxylic Acid Derivatives: Pentacyclic Compounds;156
1.7.6;Carbonic or Carboxylic Acid Derivatives: Hexacyclic Compounds;163
1.7.7;Carbonic or Carboxylic Acid Derivatives: Polycyclic Compounds;164
1.8;Name Reaction Index;166
1.8.1;A;166
1.8.2;B;166
1.8.3;C;167
1.8.4;D;168
1.8.5;E;169
1.8.6;F;169
1.8.7;G;170
1.8.8;H;170
1.8.9;I;171
1.8.10;J;171
1.8.11;K;171
1.8.12;L;171
1.8.13;M;172
1.8.14;N;173
1.8.15;O;173
1.8.16;P;174
1.8.17;R;174
1.8.18;S;175
1.8.19;T;176
1.8.20;U;176
1.8.21;V;176
1.8.22;W;176
1.8.23;Y;178
1.8.24;Z;178
1.9;Keyword Index;180
1.9.1;A;180
1.9.2;B;270
1.9.3;C;292
1.9.4;D;333
1.9.5;E;347
1.9.6;F;370
1.9.7;G;376
1.9.8;H;380
1.9.9;I;386
1.9.10;J;404
1.9.11;K;404
1.9.12;L;457
1.9.13;M;467
1.9.14;N;480
1.9.15;O;489
1.9.16;P;502
1.9.17;Q;540
1.9.18;R;542
1.9.19;S;542
1.9.20;T;558
1.9.21;U;578
1.9.22;V;580
1.9.23;W;581
1.9.24;X;584
1.9.25;Y;584
1.9.26;Z;585
1.10;Author Index;586
1.10.1;A;586
1.10.2;B;599
1.10.3;C;627
1.10.4;D;646
1.10.5;E;662
1.10.6;F;668
1.10.7;G;680
1.10.8;H;698
1.10.9;I;720
1.10.10;J;726
1.10.11;K;733
1.10.12;L;762
1.10.13;M;778
1.10.14;N;810
1.10.15;O;821
1.10.16;P;829
1.10.17;Q;845
1.10.18;R;846
1.10.19;S;862
1.10.20;T;903
1.10.21;U;919
1.10.22;V;921
1.10.23;W;929
1.10.24;X;944
1.10.25;Y;945
1.10.26;Z;952
1.11;Abbreviations;960
1.12;List of All Volumes;966

Structure Index


This index comprises a list of key cyclic substructures present in the products of Category 3 (formally carbonic and carboxylic acid derivatives).

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 series.

[3]-.-

Cyclopropane 18-41, 19-227, 20b-878, 20b-887, 20b-1145, 20b-1245, 20b-1319, 20b-1329, 22-644, 23-23, 23-128, 23-611f., 23-630, 23-658, 23-659, 23-662, 24-552
Cyclopropane, alkylidene-20b-1145, 20b-1321, 23-614, 23-620, 24-23, 24-584
Cyclopropane, acyl-20a-212, 20b-1099, 21-142, 22-62
Cyclopropanecarboxylic acid derivatives 18-100, 18-841, 18-856, 19-88, 19-198, 19-229, 19-346, 19-348, 19-364, 19-377, 19-481, 20a-58, 20a-62–20a-64, 20a-110, 20a-260, 20a-464f., 20a-475, 20a-601, 20b-690, 20b-780, 20b-1066, 20b-1195f., 20b-1378, 20b-1386f., 20b-1396, 20b-1412f., 20b-1669, 21-12, 21-61, 21-135, 21-234, 21-841f., 21-910, 22-4, 22-62, 22-67f., 22-424, 22-699, 22-727, 22-771, 23-30, 23-658, 24-52, 24-309
Cyclopropane, x-hetero-18-100, 18-151, 18-1194, 18-1228, 19-346, 19-438, 19-461, 19-481, 20a-64, 20a-260, 20a-362, 20a-512, 20b-751, 20b-1502, 22-739, 23-133, 23-720, 24-159, 24-213, 24-545

Cyclopropanone 20b-656, 20b-1502, 23-44, 23-67, 23-612, 23-627, 23-657
Cyclopropene 18-709, 18-860, 18-1065, 19-364, 23-465, 23-663, 23-696, 23-819
Cycloprop-2-en-1-one 23-698, 24-785, 24-823, 24-829f., 24-872, 24-875f., 24-926
[3]X

Oxirane 19-176, 19-269, 19-396, 20a-398, 20a-497f., 20b-728, 20b-732, 20b-740, 20b-936, 20b-1228–20b-1230, 20b-1471, 20b-1484, 20b-1502, 21-397, 22-4, 22-26, 22-237, 23-563, 24-520
Oxirane, 2-hetero-18-127, 22-67, 22-613, 23-602, 23-657, 23-668
Thiirane 18-239, 18-436, 18-870, 18-1208, 18-1232, 22-57, 22-103, 23-43, 24-509
Aziridine 18-37, 20a-84, 20a-99, 20a-472, 20b-686, 20b-1257, 22-407, 22-798, 22-800, 22-827, 24-595, 24-599f., 24-686
Aziridin-2-one 19-474, 21-9, 21-591–21-600, 22-454
2-Azirine 22-459, 23-843, 23-845

Phosphirane 19-434
1-Phosphirene 18-52, 19-10, 19-436
Iridirane 23-105
[3]2X

Oxaziridine 21-168
Dioxirane 20a-109
3-Diazirine 18-1222, 20a-96
Diphosphirane 18-288, 18-1130, 18-1229, 18-1272, 24-775
1-Diphosphirene 18-1129f.
1-Diphosphirenium 18-1130
[4]-.-

Cyclobutane 19-227, 19-348, 19-376, 20a-117, 23-128
Cyclobutane, alkylidene 19-358, 19-376, 23-635, 24-29, 24-30, 24-584
Cyclobutane, hetero-19-346, 19-376, 20a-117, 20b-1260, 20b-1389, 20b-1414, 22-450, 22-771, 23-117, 23-371, 24-29, 24-30, 24-121, 24-211, 24-213, 24-294, 24-314, 24-315
Cyclobutanone 20a-350, 20b-1500, 20b-1566, 23-2, 23-4, 23-5, 23-25, 23-32, 23-34, 23-65, 23-67, 23-78, 23-112, 23-121–23-123, 23-128, 23-130, 23-131, 23-133, 23-135, 23-137, 23-152, 23-158, 23-182, 23-184, 23-206, 23-209f., 23-266, 23-282, 23-387, 23-413, 23-414, 23-440, 23-456–23-458, 23-505, 23-509, 23-510, 23-604, 23-605, 23-612, 23-634, 23-642, 23-645–23-648, 23-670, 24-1050, 24-1082
Cyclobutane-1,3-dione 23-246, 23-248–23-250, 23-420, 23-444, 23-621, 23-623f., 23-627, 23-629, 23-630, 23-632, 23-642, 23-642–23-644, 23-649, 23-722, 23-727, 24-688

Cyclobutene 20a-3, 20a-350, 20b-1389, 20b-1413, 23-183, 23-208, 23-771, 24-52, 24-417,...

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