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1.

図書
図書
1. Macrocyclic oligoacetylenes and other linearly conjugated systems
volume editor, A. de Meijere ; with contributions by S. C. Brand ... [et al.]
出版情報: Berlin ; Tokyo : Springer, c1999  222 p. ; 25 cm
シリーズ名: Topics in current chemistry = Fortschritte der chemischen Forschung ; 201 . Carbon rich compounds ; 2
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2.

図書
図書
2. Carbon rich compounds (1)
volume editor, A. de Meijere ; with contributions by A. de Meijere ... [et al.]
出版情報: Berlin ; Tokyo : Springer, c1998  231 p. ; 24 cm
シリーズ名: Topics in current chemistry = Fortschritte der chemischen Forschung ; 196
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目次情報:
Glossary A-Z
Glossary A-Z
3.

図書
図書
3. Strain and its implications in organic chemistry : organic stress and reactivity
edited by Armin de Meijere and Siegfried Blechert
出版情報: Dordrecht ; Boston : Kluwer Academic Publishers, c1989  xviii, 525 p. ; 25 cm
シリーズ名: NATO ASI series ; ser. C . Mathematical and physical sciences ; v. 273
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4.

図書
図書
4. Organometallics in organic synthesis : aspects of a modern interdisciplinary field (: U.S. ; : Germany)
A. de Meijere, H. tom Dieck (ed.) ; contributors, R. Aumann ... [et al.]
出版情報: Berlin ; Tokyo : Springer-Verlag, c1988  vi, 320 p. ; 25 cm
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5.

図書
図書
5. Small ring compounds in organic synthesis (1 : us - 6 : ger)
guest editor, A. de Meijere
出版情報: Berlin ; Tokyo : Springer-Verlag, c1986-  v. ; 25 cm
シリーズ名: Topics in current chemistry = Fortschritte der chemischen Forschung ; 133, 135, 144, 155, 178, 207
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6.

図書
図書
6. Handbook of organopalladium chemistry for organic synthesis (v. 1 ; v. 2)
edited by Ei-ichi Negishi ; A. de Meijere, associate editor ; editorial board, J.E. Bäckvall ... [et al.]
出版情報: New York ; Chichester : Wiley, c2002  2 v. (xxxv, 3279 p.) ; 26 cm
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目次情報: 続きを見る
Preface
Contributors
Abbreviations
Volume 1
Introduction And Background / I：
Historical Background of Organopalladium Chemistry / Ei-ichi NegishiI.1：
Fundamental Properties of Palladium and Patterns of the Reactions of Palladium and Its Complexes / I.2：
Palladium Compounds: Stoichiometric Preparation, In Situ Generation, And Some Physical And Chemical Properties / II：
Background for Part II 39 / II.1：
Pd(0) and Pd(II) Compounds without Carbon-Palladium Bonds / II.2：
Metallic Palladium and Its Mixtures / II 2.1：
Palladium Complexes Containing Halogen and Oxygen Ligands / II 2.2：
Pd(0) and Pd(II) Complexes Containing Phosphorus and Other Group 15 Atom Ligands / Danietilde;le ChoueiryII 2.3：
Pd(0) and Pd(II) Complexes Containing Sulfur and Selenium Ligands / Kunio HiroiII 2.4：
Hydridopalladium Complexes / King Kuok (Mimi)Hii)II 2.5：
Palladium Complexes Containing Metal Ligands / Koichiro Oshima)II 2.6：
Chiral Pd(0) and Pd(II) Complexes / Masamichi Ogasawara ; Tamio HayashiII 2.7：
Organopalladium Compounds Containing Pd(0) and Pd(II) / II.3：
General Discussion of the Methods of Synthesis and in-Situ Generation of Organopalladium Compounds / II 3.1：
Stoichiometric Synthesis and Some Notable Properties of Organopalladium Compounds of Pd(0) and Pd(II) / II 3.2：
Palladium Complexes Containing Pd(I), Pd(III), or Pd(IV) / Allan J. CantyII.4：
Palladium-Catalyzed Reactions Involving Reductive Elimination / III：
Background for Part III / III 1：
Palladium-Catalyzed Carbon-Carbon Cross-Coupling / III 2：
Overview of the Negishi Protocol with Zn, Al, Zr, and Related Metals / III 2.1：
Overview of the Suzuki Protocol with B / Akira SuzukiIII 2.2：
Overview of the Stille Protocol with Sn / Masanori Kosugi ; Keigo FugamiIII 2.3：
Overview of Other Palladium-Catalyzed Cross-Coupling Protocols / Tamejiro Hiyama ; Eiji ShirakawaIII 2.4：
Palladium-Catalyzed Aryl-Aryl Coupling / Luigi AnastasiaIII 2.5：
Palladium-Catalyzed Alkenyl-Aryl, Aryl-Alkenyl, and Alkenyl-Alkenyl Coupling Reactions / Shouquan HuoIII 2.6：
Heteroaromatics via Palladium-Catalyzed Cross-Coupling / Kjell UndheimIII 2.7：
Palladium-Catalyzed Alkynylation / III 2.8：
Sonogashira Alkyne Synthesis / Kenkichi SonogashiraIII 2.8.1：
Palladium-Catalyzed Alkynylation with Alkynylmetals and Alkynyl Electrophiles / Carding XuIII 2.8.2：
Palladium-Catalyzed Cross-Coupling between Allyl, Benzyl, or Propargyl Groups and Unsaturated Groups / Fang LiuIII 2.9：
Palladium-Catalyzed Cross-Coupling between Allyl-, Benzyl-, or Propargylmetals and Allyl, Benzyl, or Propargyl Electrophiles / Baiqiao LiaoIII 2.10：
Palladium-Catalyzed Cross-Coupling Involving Alkylmetals or Alkyl Electrophiles / III 2.11：
Palladium-Catalyzed Cross-Coupling Involving Saturated Alkylmetals / Sebastien GagneurIII 2.11.1：
Reactions between Homoallyl-, Homopropargyl-, or Homobenzylmetals and Alkenyl or Aryl Electrophiles / Fanxing ZengIII 2.11.2：
Palladium-Catalyzed Cross-Coupling Involving alpha;-Hetero-Substituted Organic Electrophiles / III 2.12：
Palladium-Catalyzed Cross-Coupling with Acyl Halides and Related Electrophiles / Takumichi SugiharaIII 2.12.1：
Palladium-Catalyzed Cross-Coupling with Other alpha;-Hetero-Substituted Organic Electrophiles / III 2.12.2：
Palladium-Catalyzed Cross-Coupling Involving alpha;-Hetero-Substituted Organometals / III 2.13：
Palladium-Catalyzed Cross-Coupling Involving Metal Cyanides / Kentaro TakagiIII 2.13.1：
Other alpha;-Hetero-Substitu / III 2.13.2：
Preface
Contributors
Abbreviations
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