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1.Synthesis,Pyrolytic and Photolytic Study of Furo[3,2-c] Pyran-4-one 2.Pyrolytic Study of Benzoic 1,2-Dimethyl-3-Indoly AnhydrideHuang, Chi-Tsung 07 December 2004 (has links)
(1)Flash vaccum pyrolysis of furo[3,2-c]pyran-4-one gave starting material, but in photolytic system we gave a isomer: furo[2,3-c]pyran-5-one.
(2)Flash vaccum pyrolysis of benzoic 1,2-dimethyl-3-indoly anhydride,via a ketene intermediate,gave a dimmer.
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Pyrolytic Study of 2-Azidocycloheptanone and 2-[2-(4-Methoxyphenyl)vinyl]benzofuranWu, Bo-Jian 18 June 2005 (has links)
Flash vacuum pyrolysis (FVP) of 2-azidocycloheptanone gave two products: 3,4,5,6-tetrahydro-1H-azocin-2-one and 1-hydroxy-2-oxo-4- azabicyclo[5.3.0]dec-4-ene-3-spiro-2¡¦-cycloheptanone.
Flash vacuum pyrolysis of 2-[2-(4-methoxyphenyl)vinyl]benzofuran gave two products: 4-(2-benzofuran-2-ylvinyl)phenol and 1H-6-oxacyclopenta[c]fluorine.
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Pyrolytic Study of 1-Azidoindene and 3-(4-Methoxystyryl)thiopheneHsueh, Yu-tan 30 August 2005 (has links)
Flash vacuum pyrolysis (FVP) of 1-azidoindene, which via a nitrene intermediate, gave some products of rearrangement¡Gquinoline¡Bisoquinoline and 1-methylene-1H-isoindole¡CUnder pyrolytic conditions, 3-(4-methoxystyryl)thiophene could get a radical intermediate and gave 3-(4-hydroxystyryl)thiophene, or it gave contractive tricyclic compounds which having signals on spectrum but inseparable, like as indene structures.
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FLASH Industry Analysis and Competitive Strategic ResearchChang, Ming-Che 21 July 2006 (has links)
The CAGR (Compound Annual Growth Rate) of FLASH has been just like DRAMs in the past year. This product has become a typical product in the semiconductor industry. There have already been a lot of theses to study DRAM. Based on FLASH development in recent years, this thesis will determine what the successful key factors are and how Taiwan¡¦s companies have entered into this industry.
Collecting data from second hand information, this thesis will discuss Moore¡¦s law to study the impact and innovation of semiconductor in the past 40 years. According to Porter¡¦s Five Forces Model (1980), in practice this research will probe the technological evolution, industry structure, market demand, and competition relative to three success key factors- Intellectual Property, Technology Node and Economies of Scale.
Following Porter's Diamond(1990), we reveal that Taiwan¡¦s FLASH industry should cooperate with a DRAM partner and develop critical intelligent property in order to exchange licenses with a leading company.
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1. Pyrolytic Study of Arylmethylazides 2. Pyrolytic Study of 2-Amino-3-methylpyridine and its DerivativesLee, Chin-Fan 27 June 2001 (has links)
Flash vacuum pyrolysis(FVP) of azidomethylthiophene,via a nitrene intermediate,gave two products,a dimer (thienylmethylidene-thienylamine) and a trimer (N,N`-dithienyl methylidene-thienylmethylidene diamine).The trimer underwent cyclization and dehydrogenation to afford 2,4,5-trithienylimidazole. However by the same route, FVP of azidomethylbenzo[b]furan produced only a trimer(dibenzo[b]furylmethylidene-N,N'-benzo[b]furylmethyl amine).
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Pyrolytic Study of Benzoic 5-Benzyl-2-furoic Anhydride and 2-(2-Azidoethyl)thiopheneShiue, Jiing-Chyuan 30 July 2001 (has links)
(1)
The pyrolysis of benzoic 5-benzyl-2-furoic anhydride by using SS-FVP method can obtain the ring-opened product naphthalene, and no ring-contracted product and its further derivatives.
(2)
Flash vacuum pyrolysis (FVP) of 2-(2-azidoethyl)thiophene, via a nitrene intermediate gave 1,2-di(2-thienyl)ethane, 3,5-di(2-thienyl)pyridine, and 2-methylthiophene as the main products.
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1. Pyrolytic Study of (5-Methyl-2-selenophenyl)methyl Benzoate 2. Pyrolytic Study of 2-AzidomethylselenopheneChu, Chung-chen 27 June 2002 (has links)
(1) Flash vacuum pyrolysis (FVP) of (5-methyl-2-selenophenyl)methyl benzoate gave 4-methylene-4H-selenopyran. The structure was confirmed by trapping experiment. The mechanism for the 4-methylene-4H-selenopyran will be discussed.
(2) Flash vacuum pyrolysis of 2-Azidomethylselenophene, via a nitrene intermediate, gave a trimer (N,N¡¦-di-2-selenophenylmethylidene-2-selenophenylmethylidene diamine).
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Pyrolytic Study of 2-Azidoacetophenone and 2-Azido-1-(2-thienyl)ethanoneLin, Tsung-Te 02 July 2002 (has links)
Flash vacuum pyrolysis (FVP) of 2-azidoacetophenone gave the dimer 2-benzoyl-4- phenylimidazole and the trimer: 2,3-dibenzoyl-5-phenylpyrazine.
Flash vacuum pyrolysis of 2-azido-1-(2-thienyl)ethanone gave the dimer: 2-(2-fromylthienyl)-4-(2-thienyl)imidazole and 2-formylthiophene.
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Pyrolytic Study of 2-Azido-1-(1-methyl-2-pyrryl)ethanone and 2-Azido-1-(2-benzo[b]thienyl)ethanoneLin, Hsiao-Yu 26 June 2003 (has links)
Flash vacuum pyrolysis (FVP) of 2-azido-1-(1-methyl-2-pyrryl)ethanone and 2-azido-1- (2-benzo[b]thienyl)ethanone gave nitrene by elimination of one nitrogen molecule.
When 2-azido-1-(1-methyl-2-pyrryl)ethanone as a precorsor, the reactive nitrene readily underwent self-condensation to give 2-(1-methyl-2-formylpyrryl)-4-(1-methyl-2- pyrryl)imidazole, it¡¦s isomer and 2,4,5-tri(1-methyl-2-formylpyrryl) imidazole. While 2-azido-1-(2-benzo[b]thienyl)ethanone as a precorsor, the reactive nitrene readily underwent self-condensation to give 2-2-formylbenzo[b]thienyl-5-(2-benzo[b]thiophen-2-yl)imidazole.
The mechanism for the formation of products of self-condensation reaction from FVP of 2-azido-1-(1-methyl-2-pyrryl)ethanone and 2-azido-1-(2-benzo[b]thienyl) ethanone will be discussed.
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(¤@) Pyrolytic and Photolytic Studies of o-Thiomethoxystilbene and Its Derivatives (¤G) Synthetic Study of Thieno-Fused Derivatives of TruxeneLiou, Yi-Ke 01 July 2008 (has links)
Abstract¡G
¤@¡B trans o-Thiomethoxystilbene and its derivatives 19a-c had been studied by means of pyrolysis and photolysis. Under pyrolytic conditions, compounds 19a-c gave not only the products 24¡B30¡B33,but also their corresponding isomers 26¡B31¡B34 . Furthermore, compound 19c gave dibenzothiophene (32) as the major product by opening the furan ring at higher temperature. Under photolytic conditions, compounds 19a-c gave the corresponding photocyclic products 40¡B44¡B46. With the exception of 19c, photolysis of 19a and 19b also gave 24 and 30, respectively.
¤G¡B For synthetic study of thieno-fused derivatives 4 and 5 of truxene, preparation monomer 6 and 7 can be accomplished in two steps by means of flash vacuum pyrolysis.
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