Organic synthesis: state of the art 2005-2007
Gespeichert in:
1. Verfasser: | |
---|---|
Format: | Buch |
Sprache: | English |
Veröffentlicht: |
Hoboken, NJ
Wiley
2008
|
Schlagworte: | |
Online-Zugang: | Inhaltsverzeichnis |
Beschreibung: | Includes indexes. |
Beschreibung: | XI, 228 S. Ill. 25 cm |
ISBN: | 9780470288498 0470288493 |
Internformat
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100 | 1 | |a Taber, Douglass F. |e Verfasser |4 aut | |
245 | 1 | 0 | |a Organic synthesis |b state of the art 2005-2007 |c Douglass F. Taber |
264 | 1 | |a Hoboken, NJ |b Wiley |c 2008 | |
300 | |a XI, 228 S. |b Ill. |c 25 cm | ||
336 | |b txt |2 rdacontent | ||
337 | |b n |2 rdamedia | ||
338 | |b nc |2 rdacarrier | ||
500 | |a Includes indexes. | ||
650 | 4 | |a Organic compounds |x Synthesis | |
650 | 4 | |a Organic compounds |x Synthesis |x Research | |
650 | 0 | 7 | |a Organische Synthese |0 (DE-588)4075695-6 |2 gnd |9 rswk-swf |
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999 | |a oai:aleph.bib-bvb.de:BVB01-016507653 |
Datensatz im Suchindex
_version_ | 1804137663499862016 |
---|---|
adam_text | Contents
Preface
xi
1.
Synthesis of
(-)-
Littoralisone
1
2.
Enantiocontrolled Construction of Oxygenated and Animated
3
Stereogenic Centers
3.
Catalytic Enantioselecti
ve
Construction of Alkylated
5
Stereogenic Centers
4.
Catalytic Eriantioselective Aldol/Mannich Reactions Leading to
7
Extended Arrays of Stereogenic Centers
5.
Alternative Strategies for the Construction of Extended Arrays of
9
Stereogenic Centers
6.
Synthesis ofC-)- Avrainvillamide and
(+)-
Stephacidin
В
11
7.
Best Synthetic Methods: Oxidation
13
8.
Best Synthetic Methods: Reduction
15
9.
Selective Reactions of Alkenes
17
10.
Synthesis of the Potent FBBP
12
Ligand Antascomicin
В
19
11.
Best Synthetic Methods: Carbon-Carbon Bond Formation
21
12.
Enantioselective Construction of Quaternary Centers
23
13.
Pd-Mediated Arylation of Aromatic and
Hetero
Aromatic Rings
25
14.
The Overman Route to Gelsemine
27
15.
Stereoselective Construction of Oxygen Heterocycles
29
16.
Enantioselective Construction of Naturally-Occurring
31
Cyclic Ethers
17.
Stereoselective Construction of Nitrogen Heterocycles
33
18.
The Stork Synthesis of
(-)-
Reserpine
35
19.
Stereocontrolled Construction of Azacyclic Natural Products
37
20.
Preparation of Benzene Derivatives
39
21.
Preparation of Heteroaromatics
41
Contents
22.
Preparation and Reactions of Carboxylic Acids, Esters and Amides
43
23.
The
Boger
Route to
(-)-
Vindoline
45
24.
Protection of
C
-О
and C-N
47
25.
New Catalysts and Strategies for Alkene Metathesis
49
26.
Creative Applications of Alkene and Alkyne Metathesis in Total
51
Synthesis: (+)-8-ep/-Xanthatin, (+)-Longicin, Latranculin A, and
Garsubellin A
27.
Synthesis of Erythronolide A
53
28.
Best Synthetic Methods:
C
-С
Bond Formation
55
29.
Catalytic Enantioselective
Homologation
of Aldehydes to Alcohols
57
and Amines
30.
Catalytic Enantioselective Construction of Alkylated Stereogenic
59
Centers
31.
Enantioselective Construction of Arrays of Stereogenic Centers
61
32.
Adventures in Complex
Indole
Synthesis: (-)-Fischerindole I,
63
(+)-Fischerindole
G
and (+)-Weltwitindolinone A
33.
New Dienes and Dienophiles for Intermolecular and Intramolecular
65
Diels-Alder Cycloaddtions
34.
Organocatalytic Preparation of Enantiomerically-PureCarbocycles
67
35.
Carbocycle Construction by the Opening of Strained Rings: Synthesis
69
of Tremulenolide A
36.
The Corey Route to the Dolabellanes: Isoedunol and
ß-Araneosene 71
37.
Transition-Metal Catalyzed Enantioselective Ring Construction
73
38.
Best Synthetic Methods: Functional Group Transformation
75
39.
Selective Reactions of Alkenes
77
40.
Synthesis and Absolute Stereochemical Assignment of
79
(-)-Galbulimima Alkaloid
13
41.
Preparation of Benzene Derivatives
81
42.
Preparation of Heteroaromatic Derivatives
83
43.
Functional Group Transformation
85
44.
Functional Group Protection
87
45.
The Leighton Synthesis of Dolabelide
D
89
vi
Contents
46.
Stereocontrolled Construction of
N-Heterocycles 91
47.
Stereocontrolled Construction of O-Heterocycles
93
48.
Stereocontrolled Synthesis of O-Heterocyclic Natural Products
95
49.
The Ready Synthesis of (-)-Nigellamine A2
97
50.
Advances in the Diels-Alder Reaction: Synthesis of (+)-Lycoridine
99
and of Dolabellatrienone
51.
Enantioselective Carbocyclic Construction
101
52.
Transition Metal Mediated Carbocyclic Construction
103
53.
Synthesis of (-J-Colombiasin A and (-)-Elisapterosin
В
105
54.
Enantioselective Synthesis of
С
-N
Ring Containing Natural Products
107
55.
New Catalysts and Strategies for Alkene and Alkyne Metathesis
109
56.
Heterocyclic Natural Products by Alkene Metathesis 111
57.
Carbobyclic Natural Products by Alkene Metathesis
113
58.
The Crimmins Synthesis of (+)-SCH
351448 115
59.
Enantioselective Construction of Alcohols and Amines
117
61.
Enantioselective Construction of Alkylated Stereogenic Centers
119
61.
Enantioselective Construction of Arrays of Stereogenic Centers
121
62.
The Sorensen Synthesis of
(-)-Guanacastepene E
123
63.
Selective Reactions of
Alkenes
125
64.
Best Synthetic Methods:
C-C
Bond Formation
127
65.
Functional Group Protection and Deprotection
129
66.
The Nicolaou Synthesis of Platensimycin
131
67.
Stereocontrolled C-0 Ring Construction
133
68.
Stereocontrolled Natural Product Synthesis: Cyclic Ethers and
135
Macrolides
69.
Stereocontrolled
С
-N
Ring Construction
137
70.
Stereocontrolled Alkaloid Total Synthesis
139
71.
The Fukuyama Synthesis of Morphine
141
73.
Oxidation and Reduction in Organic Synthesis
143
73.
Interconversion
of Organic Functional Groups
145
vii
Contents
74.
Best Synthetic Methods: Carbon-Carbon Bond Formation
147
75.
The Overman Synthesis of (-)-Sarain A
149
76.
Recent Developments in Alkene Metathesis
151
77.
Pushing the Limits of Alkene Metathesis in Natural Product Synthesis
153
78.
Preparation of Benzene Derivatives
155
79.
The
Padwa
Synthesis of Aspidophytidine
157
80.
Synthesis of Heteroaromatics
159
81.
Enantioselective Construction of Alcohols and Amines
161
82.
Enantioselective Construction of Alkylated Stereogenic Centers
163
83.
Enantioselective Construction of Arrays of Stereogenic Centers
165
84.
The Gin Synthesis of
Nominine
167
85.
The Intramolecular Diels-Alder Reaction in Natural Product
169
Synthesis
86.
Catalytic Enantioselective Carbon-Carbon Ring Construction
171
87.
New Directions in
C
-С
Ring Construction: The Overman Synthesis of
173
Guanacastepene
N
88.
The
Petrus
Synthesis of (+)-Rishirilide
В
175
89.
Selective Reactions of
Alkenes
177
90.
Selective
C
-Н
Functionalization
179
91.
New Methods for Carbon-Carbon Bond Formation
181
92.
The Nakada Synthesis of (+)-Digitoxigenin
183
93.
Preparation of Benzene Derivatives
185
94.
Preparation of Heteroaromatics: The Movassaghi Synthesis of
187
(+)-Chimonanthine
95.
Organic Functional Group Transformation
189
96.
Organic Functional Group Protection
191
97.
The
Trost
Synthesis of O-Terpestacin
193
98.
Stereoselective
С
-N
Ring Construction
195
99.
Stereoselective C-0 Ring Construction
197
100.
Synthesis of O-Blepharocalyxin D, (-J-Lasonolide A, and Attenol A
199
viii
Contents
101.
The Dark Synthesis of Vigulariol
201
102.
Enantioselective Organocatalytic Synthesis of Carbocycles: The
203
Iwabuchi Synthesis of (+)-Juvabione
103.
Transition-metal Mediated Synthesis of Carbocycles: The Snapper
205
Synthesis of Pleocarpenone
104.
Enantioselective Construction of Carbocycles: The Williams
207
Synthesis of (+)-Fusicoauritone
105.
C
-Н
Functionalization: The White Reagent
207
Author Index
209
Reaction Index
219
IX
|
adam_txt |
Contents
Preface
xi
1.
Synthesis of
(-)-
Littoralisone
1
2.
Enantiocontrolled Construction of Oxygenated and Animated
3
Stereogenic Centers
3.
Catalytic Enantioselecti
ve
Construction of Alkylated
5
Stereogenic Centers
4.
Catalytic Eriantioselective Aldol/Mannich Reactions Leading to
7
Extended Arrays of Stereogenic Centers
5.
Alternative Strategies for the Construction of Extended Arrays of
9
Stereogenic Centers
6.
Synthesis ofC-)- Avrainvillamide and
(+)-
Stephacidin
В
11
7.
Best Synthetic Methods: Oxidation
13
8.
Best Synthetic Methods: Reduction
15
9.
Selective Reactions of Alkenes
17
10.
Synthesis of the Potent FBBP
12
Ligand Antascomicin
В
19
11.
Best Synthetic Methods: Carbon-Carbon Bond Formation
21
12.
Enantioselective Construction of Quaternary Centers
23
13.
Pd-Mediated Arylation of Aromatic and
Hetero
Aromatic Rings
25
14.
The Overman Route to Gelsemine
27
15.
Stereoselective Construction of Oxygen Heterocycles
29
16.
Enantioselective Construction of Naturally-Occurring
31
Cyclic Ethers
17.
Stereoselective Construction of Nitrogen Heterocycles
33
18.
The Stork Synthesis of
(-)-
Reserpine
35
19.
Stereocontrolled Construction of Azacyclic Natural Products
37
20.
Preparation of Benzene Derivatives
39
21.
Preparation of Heteroaromatics
41
Contents
22.
Preparation and Reactions of Carboxylic Acids, Esters and Amides
43
23.
The
Boger
Route to
(-)-
Vindoline
45
24.
Protection of
C
-О
and C-N
47
25.
New Catalysts and Strategies for Alkene Metathesis
49
26.
Creative Applications of Alkene and Alkyne Metathesis in Total
51
Synthesis: (+)-8-ep/-Xanthatin, (+)-Longicin, Latranculin A, and
Garsubellin A
27.
Synthesis of Erythronolide A
53
28.
Best Synthetic Methods:
C
-С
Bond Formation
55
29.
Catalytic Enantioselective
Homologation
of Aldehydes to Alcohols
57
and Amines
30.
Catalytic Enantioselective Construction of Alkylated Stereogenic
59
Centers
31.
Enantioselective Construction of Arrays of Stereogenic Centers
61
32.
Adventures in Complex
Indole
Synthesis: (-)-Fischerindole I,
63
(+)-Fischerindole
G
and (+)-Weltwitindolinone A
33.
New Dienes and Dienophiles for Intermolecular and Intramolecular
65
Diels-Alder Cycloaddtions
34.
Organocatalytic Preparation of Enantiomerically-PureCarbocycles
67
35.
Carbocycle Construction by the Opening of Strained Rings: Synthesis
69
of Tremulenolide A
36.
The Corey Route to the Dolabellanes: Isoedunol and
ß-Araneosene 71
37.
Transition-Metal Catalyzed Enantioselective Ring Construction
73
38.
Best Synthetic Methods: Functional Group Transformation
75
39.
Selective Reactions of Alkenes
77
40.
Synthesis and Absolute Stereochemical Assignment of
79
(-)-Galbulimima Alkaloid
13
41.
Preparation of Benzene Derivatives
81
42.
Preparation of Heteroaromatic Derivatives
83
43.
Functional Group Transformation
85
44.
Functional Group Protection
87
45.
The Leighton Synthesis of Dolabelide
D
89
vi
Contents
46.
Stereocontrolled Construction of
N-Heterocycles 91
47.
Stereocontrolled Construction of O-Heterocycles
93
48.
Stereocontrolled Synthesis of O-Heterocyclic Natural Products
95
49.
The Ready Synthesis of (-)-Nigellamine A2
97
50.
Advances in the Diels-Alder Reaction: Synthesis of (+)-Lycoridine
99
and of Dolabellatrienone
51.
Enantioselective Carbocyclic Construction
101
52.
Transition Metal Mediated Carbocyclic Construction
103
53.
Synthesis of (-J-Colombiasin A and (-)-Elisapterosin
В
105
54.
Enantioselective Synthesis of
С
-N
Ring Containing Natural Products
107
55.
New Catalysts and Strategies for Alkene and Alkyne Metathesis
109
56.
Heterocyclic Natural Products by Alkene Metathesis 111
57.
Carbobyclic Natural Products by Alkene Metathesis
113
58.
The Crimmins Synthesis of (+)-SCH
351448 115
59.
Enantioselective Construction of Alcohols and Amines
117
61.
Enantioselective Construction of Alkylated Stereogenic Centers
119
61.
Enantioselective Construction of Arrays of Stereogenic Centers
121
62.
The Sorensen Synthesis of
(-)-Guanacastepene E
123
63.
Selective Reactions of
Alkenes
125
64.
Best Synthetic Methods:
C-C
Bond Formation
127
65.
Functional Group Protection and Deprotection
129
66.
The Nicolaou Synthesis of Platensimycin
131
67.
Stereocontrolled C-0 Ring Construction
133
68.
Stereocontrolled Natural Product Synthesis: Cyclic Ethers and
135
Macrolides
69.
Stereocontrolled
С
-N
Ring Construction
137
70.
Stereocontrolled Alkaloid Total Synthesis
139
71.
The Fukuyama Synthesis of Morphine
141
73.
Oxidation and Reduction in Organic Synthesis
143
73.
Interconversion
of Organic Functional Groups
145
vii
Contents
74.
Best Synthetic Methods: Carbon-Carbon Bond Formation
147
75.
The Overman Synthesis of (-)-Sarain A
149
76.
Recent Developments in Alkene Metathesis
151
77.
Pushing the Limits of Alkene Metathesis in Natural Product Synthesis
153
78.
Preparation of Benzene Derivatives
155
79.
The
Padwa
Synthesis of Aspidophytidine
157
80.
Synthesis of Heteroaromatics
159
81.
Enantioselective Construction of Alcohols and Amines
161
82.
Enantioselective Construction of Alkylated Stereogenic Centers
163
83.
Enantioselective Construction of Arrays of Stereogenic Centers
165
84.
The Gin Synthesis of
Nominine
167
85.
The Intramolecular Diels-Alder Reaction in Natural Product
169
Synthesis
86.
Catalytic Enantioselective Carbon-Carbon Ring Construction
171
87.
New Directions in
C
-С
Ring Construction: The Overman Synthesis of
173
Guanacastepene
N
88.
The
Petrus
Synthesis of (+)-Rishirilide
В
175
89.
Selective Reactions of
Alkenes
177
90.
Selective
C
-Н
Functionalization
179
91.
New Methods for Carbon-Carbon Bond Formation
181
92.
The Nakada Synthesis of (+)-Digitoxigenin
183
93.
Preparation of Benzene Derivatives
185
94.
Preparation of Heteroaromatics: The Movassaghi Synthesis of
187
(+)-Chimonanthine
95.
Organic Functional Group Transformation
189
96.
Organic Functional Group Protection
191
97.
The
Trost
Synthesis of O-Terpestacin
193
98.
Stereoselective
С
-N
Ring Construction
195
99.
Stereoselective C-0 Ring Construction
197
100.
Synthesis of O-Blepharocalyxin D, (-J-Lasonolide A, and Attenol A
199
viii
Contents
101.
The Dark Synthesis of Vigulariol
201
102.
Enantioselective Organocatalytic Synthesis of Carbocycles: The
203
Iwabuchi Synthesis of (+)-Juvabione
103.
Transition-metal Mediated Synthesis of Carbocycles: The Snapper
205
Synthesis of Pleocarpenone
104.
Enantioselective Construction of Carbocycles: The Williams
207
Synthesis of (+)-Fusicoauritone
105.
C
-Н
Functionalization: The White Reagent
207
Author Index
209
Reaction Index
219
IX |
any_adam_object | 1 |
any_adam_object_boolean | 1 |
author | Taber, Douglass F. |
author_facet | Taber, Douglass F. |
author_role | aut |
author_sort | Taber, Douglass F. |
author_variant | d f t df dft |
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callnumber-label | QD262 |
callnumber-raw | QD262 |
callnumber-search | QD262 |
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callnumber-subject | QD - Chemistry |
classification_rvk | VK 5500 |
classification_tum | CHE 620f |
ctrlnum | (OCoLC)182736467 (DE-599)BSZ282441786 |
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dewey-hundreds | 500 - Natural sciences and mathematics |
dewey-ones | 547 - Organic chemistry |
dewey-raw | 547.2 |
dewey-search | 547.2 |
dewey-sort | 3547.2 |
dewey-tens | 540 - Chemistry and allied sciences |
discipline | Chemie / Pharmazie Chemie |
discipline_str_mv | Chemie / Pharmazie Chemie |
format | Book |
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id | DE-604.BV023323601 |
illustrated | Illustrated |
index_date | 2024-07-02T20:54:37Z |
indexdate | 2024-07-09T21:15:52Z |
institution | BVB |
isbn | 9780470288498 0470288493 |
language | English |
oai_aleph_id | oai:aleph.bib-bvb.de:BVB01-016507653 |
oclc_num | 182736467 |
open_access_boolean | |
owner | DE-703 DE-91G DE-BY-TUM DE-11 |
owner_facet | DE-703 DE-91G DE-BY-TUM DE-11 |
physical | XI, 228 S. Ill. 25 cm |
publishDate | 2008 |
publishDateSearch | 2008 |
publishDateSort | 2008 |
publisher | Wiley |
record_format | marc |
spelling | Taber, Douglass F. Verfasser aut Organic synthesis state of the art 2005-2007 Douglass F. Taber Hoboken, NJ Wiley 2008 XI, 228 S. Ill. 25 cm txt rdacontent n rdamedia nc rdacarrier Includes indexes. Organic compounds Synthesis Organic compounds Synthesis Research Organische Synthese (DE-588)4075695-6 gnd rswk-swf Organische Synthese (DE-588)4075695-6 s DE-604 Digitalisierung UB Bayreuth application/pdf http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=016507653&sequence=000002&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA Inhaltsverzeichnis |
spellingShingle | Taber, Douglass F. Organic synthesis state of the art 2005-2007 Organic compounds Synthesis Organic compounds Synthesis Research Organische Synthese (DE-588)4075695-6 gnd |
subject_GND | (DE-588)4075695-6 |
title | Organic synthesis state of the art 2005-2007 |
title_auth | Organic synthesis state of the art 2005-2007 |
title_exact_search | Organic synthesis state of the art 2005-2007 |
title_exact_search_txtP | Organic synthesis state of the art 2005-2007 |
title_full | Organic synthesis state of the art 2005-2007 Douglass F. Taber |
title_fullStr | Organic synthesis state of the art 2005-2007 Douglass F. Taber |
title_full_unstemmed | Organic synthesis state of the art 2005-2007 Douglass F. Taber |
title_short | Organic synthesis |
title_sort | organic synthesis state of the art 2005 2007 |
title_sub | state of the art 2005-2007 |
topic | Organic compounds Synthesis Organic compounds Synthesis Research Organische Synthese (DE-588)4075695-6 gnd |
topic_facet | Organic compounds Synthesis Organic compounds Synthesis Research Organische Synthese |
url | http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=016507653&sequence=000002&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA |
work_keys_str_mv | AT taberdouglassf organicsynthesisstateoftheart20052007 |