1. Approach to the kempane skeleton via intramolecular Diels-Alder cycloaddition of fulvene 2. Application of organocatalysts in Baylis-Hillman reaction and related cycloaddition
博士 === 國立中正大學 === 化學所 === 94 === Part 1: Approach to the kempane skeleton via intramolecular Diels-Alder cycloaddition of fulvene The Kempane skeletons can be prepared rapidly via intramolecular Diels-Alder cycloadditions (IMDA) of fulvenes. The chemistry upon both intramolecular Diels-Alder cyclo...
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ndltd-TW-094CCU050650192015-10-13T10:45:17Z http://ndltd.ncl.edu.tw/handle/51860899827903256040 1. Approach to the kempane skeleton via intramolecular Diels-Alder cycloaddition of fulvene 2. Application of organocatalysts in Baylis-Hillman reaction and related cycloaddition 1.利用富烯化合物進行分子內Diels-Alder環化加成反應合成Kempane骨架之研究2.有機催化劑應用在Baylis-Hillman反應及[3+3]和[4+2]環化加成反應之研究 Shang-Hong Chen 陳尚鴻 博士 國立中正大學 化學所 94 Part 1: Approach to the kempane skeleton via intramolecular Diels-Alder cycloaddition of fulvene The Kempane skeletons can be prepared rapidly via intramolecular Diels-Alder cycloadditions (IMDA) of fulvenes. The chemistry upon both intramolecular Diels-Alder cycloadditions and Prins reaction. Part 2: Application of organocatalysts in Baylis-Hillman reaction and related cycloaddition A highly enantioselective proline catalyzed intramolecular Baylis–Hillman reaction of hept-2-enedial is reported. Addition of imidazole to the mixture results in an unusual inversion of enantioselectivity. The organocatalyzed [3 + 3] and [4+2] cycloaddition of ?β-unsaturated aldehydes affored aromatic aldehydes. none 洪伯誠 2006 學位論文 ; thesis 546 zh-TW |
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博士 === 國立中正大學 === 化學所 === 94 === Part 1: Approach to the kempane skeleton via intramolecular Diels-Alder cycloaddition of fulvene
The Kempane skeletons can be prepared rapidly via intramolecular
Diels-Alder cycloadditions (IMDA) of fulvenes. The chemistry upon both intramolecular Diels-Alder cycloadditions and Prins reaction.
Part 2: Application of organocatalysts in Baylis-Hillman reaction and related cycloaddition
A highly enantioselective proline catalyzed intramolecular Baylis–Hillman reaction of hept-2-enedial is reported. Addition of imidazole to the mixture results in an unusual inversion of enantioselectivity. The organocatalyzed [3 + 3] and [4+2] cycloaddition of ?β-unsaturated aldehydes affored aromatic aldehydes.
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none Shang-Hong Chen 陳尚鴻 |
author |
Shang-Hong Chen 陳尚鴻 |
spellingShingle |
Shang-Hong Chen 陳尚鴻 1. Approach to the kempane skeleton via intramolecular Diels-Alder cycloaddition of fulvene 2. Application of organocatalysts in Baylis-Hillman reaction and related cycloaddition |
author_sort |
Shang-Hong Chen |
title |
1. Approach to the kempane skeleton via intramolecular Diels-Alder cycloaddition of fulvene 2. Application of organocatalysts in Baylis-Hillman reaction and related cycloaddition |
title_short |
1. Approach to the kempane skeleton via intramolecular Diels-Alder cycloaddition of fulvene 2. Application of organocatalysts in Baylis-Hillman reaction and related cycloaddition |
title_full |
1. Approach to the kempane skeleton via intramolecular Diels-Alder cycloaddition of fulvene 2. Application of organocatalysts in Baylis-Hillman reaction and related cycloaddition |
title_fullStr |
1. Approach to the kempane skeleton via intramolecular Diels-Alder cycloaddition of fulvene 2. Application of organocatalysts in Baylis-Hillman reaction and related cycloaddition |
title_full_unstemmed |
1. Approach to the kempane skeleton via intramolecular Diels-Alder cycloaddition of fulvene 2. Application of organocatalysts in Baylis-Hillman reaction and related cycloaddition |
title_sort |
1. approach to the kempane skeleton via intramolecular diels-alder cycloaddition of fulvene 2. application of organocatalysts in baylis-hillman reaction and related cycloaddition |
publishDate |
2006 |
url |
http://ndltd.ncl.edu.tw/handle/51860899827903256040 |
work_keys_str_mv |
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