Stereoselective Synthesis
Lectures honouring Prof. Dr. Dr. h.c. Rudolf Wiechert
Stereoselective Synthesis
Lectures honouring Prof. Dr. Dr. h.c. Rudolf Wiechert
A symposium on stereoeselective synthesis was organized by
the Schering AG to honour Professor Dr. Dr. h.c. Rudolf
Wiechert's 65th birthday and his achievements in over 30
years of successful medicinal chemistry research.
The six plenary lectures by leading scientists are published
in this book. The contributions highlight recent progress on
diastereo- and enantioselective synthesis. Intriguing
methodological work, synthesis of homochiral building blocks
and elegant and highly efficient applications to the
synthesis of stereochemically demanding targetmolecules are
presented.
From the Contents: Steroids and Stereochemistry-
Enantioselective Catalysis with Chiral Metal Complexes - New
Aspects in Stereoselective Synthesis of Aminoalcohols and
Amino Acids - Enzymemimetic C-C and C-N Bond Formations -
Synthesis of Natural Product of Polyketide Origin, An
Exemplary Case - Progress in the Diels/Alder Reaction Means
Progress in Steroid Synthesis
1. Introduction
2. Chiral C2-Symmetric Semicorrins
3. Analogues of Semicorrins: Aza-semicorrins and Bis (oxazolines)
4. Pd-Catalyzed Allylic Substitution
References
New Aspects in Stereoselective Synthesis of Aminoalcohols and Amino Acids
1. The 1-3 segment
2. The 6-Position
3. Position 9: Prolines
4. Position 6, 8 or others: BAZ
5. Conclusion
References
Enzymemimetic C-C and C-N Bond Formations
1. Introduction
2. Enzymemimetic C-C Bond Formations
3. Enzymemimetic C-N Bond Formations
4. Conclusion
References
Synthesis of Natural Products of Polyketide Origin, an Exemplary Case
1. Aims of Natural Product Synthesis, Changes over Time
2. New Methods for the Synthesis of Polyketide Derived Natural Products
3. Linear Synthesis of a Protected seco-Aacid of 9(S)-Dihydroerythronolide A
4. The Macrolactonization to 9(S)-Dihydroerythronolide A
References
Progress in the Diels/Alder Reaction Means Progress in Steroid Synthesis
1. Evaluation of the Diels/Alder Reaction: Cantharidin
2. Evaluation of the Diels/Alder Reaction: Norgestrel
3. Parerga
References.
the Schering AG to honour Professor Dr. Dr. h.c. Rudolf
Wiechert's 65th birthday and his achievements in over 30
years of successful medicinal chemistry research.
The six plenary lectures by leading scientists are published
in this book. The contributions highlight recent progress on
diastereo- and enantioselective synthesis. Intriguing
methodological work, synthesis of homochiral building blocks
and elegant and highly efficient applications to the
synthesis of stereochemically demanding targetmolecules are
presented.
From the Contents: Steroids and Stereochemistry-
Enantioselective Catalysis with Chiral Metal Complexes - New
Aspects in Stereoselective Synthesis of Aminoalcohols and
Amino Acids - Enzymemimetic C-C and C-N Bond Formations -
Synthesis of Natural Product of Polyketide Origin, An
Exemplary Case - Progress in the Diels/Alder Reaction Means
Progress in Steroid Synthesis
Steroids and Stereochemistry
Enantioselective Catalysis with Chiral Metal Complexes1. Introduction
2. Chiral C2-Symmetric Semicorrins
3. Analogues of Semicorrins: Aza-semicorrins and Bis (oxazolines)
4. Pd-Catalyzed Allylic Substitution
References
New Aspects in Stereoselective Synthesis of Aminoalcohols and Amino Acids
1. The 1-3 segment
2. The 6-Position
3. Position 9: Prolines
4. Position 6, 8 or others: BAZ
5. Conclusion
References
Enzymemimetic C-C and C-N Bond Formations
1. Introduction
2. Enzymemimetic C-C Bond Formations
3. Enzymemimetic C-N Bond Formations
4. Conclusion
References
Synthesis of Natural Products of Polyketide Origin, an Exemplary Case
1. Aims of Natural Product Synthesis, Changes over Time
2. New Methods for the Synthesis of Polyketide Derived Natural Products
3. Linear Synthesis of a Protected seco-Aacid of 9(S)-Dihydroerythronolide A
4. The Macrolactonization to 9(S)-Dihydroerythronolide A
References
Progress in the Diels/Alder Reaction Means Progress in Steroid Synthesis
1. Evaluation of the Diels/Alder Reaction: Cantharidin
2. Evaluation of the Diels/Alder Reaction: Norgestrel
3. Parerga
References.
Ottow, Eckhard
Schöllkopf, Klaus
Schulz, Bernd-Günter
ISBN | 978-3-642-78498-9 |
---|---|
Artikelnummer | 9783642784989 |
Medientyp | Buch |
Auflage | Softcover reprint of the original 1st ed. 1993 |
Copyrightjahr | 2012 |
Verlag | Springer, Berlin |
Umfang | XIV, 136 Seiten |
Abbildungen | XIV, 136 p. |
Sprache | Englisch |