Cycloproparenes /

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Cycloproparenes /

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Xehetasun bibliografikoak
Egile nagusia:	Halton, Brian.
Formatua:	Artikulua
Hizkuntza:	English
Gaiak:	Cyclopropane derivatives Organic chemistry
Etiketak:	Etiketa erantsi Etiketarik gabe, Izan zaitez lehena erregistro honi etiketa jartzen!

Thư viện lưu trữ:	Thư viện Trường Đại học Đà Lạt

Antzeko izenburuak

Structure, synthesis, chemical reactions of fluorinated cyclopropanes and cyclopropenes /
nork: Dolbier, William R., Jr.

Syntheses of gem-dihalocyclopropanes and their use in organic synthesis /
nork: Fedorynski, Michal.

Allenes from cyclopropanes and their use in organic synthesis-recent developments /
nork: Sydnes, Leiv K.

Donor-acceptor-substituted cyclopropane derivatives and their alication in organic synthesis /
nork: Reissig, Hans-Ulrich.

Thermal rearrangements of vinylcyclopropanes to cyclopentenes /
nork: Baldwin, John E.

Heterocycles from alkylidenecyclopropanes /

Cyclopropenone acetals - synthesis and reactions /
nork: Nakamura, Masaharu.

Cyclopropenylium cations, cyclopropenones, heteroanalogues-recent advances /
nork: Komatsu, Koichi.

Enantiomerically pure cyclobutane derivatives and their use in organic synthesis /
nork: Lee-Ruff, Edward.

Cyclobutarenes and related compounds /
nork: Sadana, Anil K.

Synthesis and alications of beta-aminocarboxylic acids containing a cyclopropane ring /
nork: Gnad, Frieder.

The chemistry of cyclopropanols /
nork: Kulinkovich, Oleg G.

Thermally induced cyclopropene-carbene rearrangements : An overview/
nork: Baird, Mark S.

Photoelectron spectra of cyclopropane and cyclopropene compounds /
nork: Rademacher, Paul.

Synthesis and properties of oligocyclopropyl-containing natural products and model compounds /
nork: Pietruszka, Joerg.

Biosynthesis and metabolism of cyclopropane rings in natural compounds /
nork: Wessjohann, Ludger A.

Stereoselective cyclopropanation reactions /

Introduction : Cyclopropanes and related rings /
nork: Meijere, Armin de.

The alication of cyclobutane derivatives in organic synthesis /
nork: Namyslo, Jan C.

Construction of pyridine rings by metal-mediated [2+2+2] cycloaddition /
nork: Varela, Jesus A.

Peptide nucleic acids :
Argitaratua: (2002)

A field-dependent organic LED consisting of two new high Tg blue light emitting organic layers : A possibility of attainment of a white light source /
nork: Cha, Soon Wook.

Novel heterocycle-based organic molecules with two-photon induced blue fluorescent emission /

Liquid crystalline cyclic tetramethyltetrasiloxanes containing coumarin moieties /
nork: Tian, Yanqing.

Congener-specific composition of polychlorinated naphthalenes, coplanar PCBs, dibenzo-p-dioxins, dibenzofurans in the halowax series /
nork: Noma, Yukio.

Formation of dioxins in the catalytic combustion of chlorobenzene and a micropollutant-like mixture on Pt/gamma-Al2O3 /
nork: Jong, Vincent De.

Derivatives markets
nork: McDonald, Robert L.
Argitaratua: (2003)

Credit derivatives :
Argitaratua: (2004)

Financial derivatives :
nork: Baz, Jamil
Argitaratua: (2003)

Study guide and manual for Organic chemistry /
nork: Schore, Neil E.
Argitaratua: (1999)

Organic chemistry : structure and function /
nork: Vollhardt, K. Peter C.
Argitaratua: (1999)

Organic chemistry /
nork: McMurry, John.
Argitaratua: (2000)

Fundamentals of organic chemistry /
nork: McMurry, John.
Argitaratua: (1998)

Synthesis, photoluminescence and electroluminescence of new 1H-pyrazolo[3,4-b]quinoxaline derivatives /

Assessing influence of experimental parameters on formation of PCDD/F from ash derived from fires of CCA-treated wood /
nork: Tame, N. W.

Formation of dioxins from incineration of foods found in domestic garbage /
nork: Katami, Takeo.

Latent ultraviolet light absorbers /
nork: Kocher, Christoph.

Derivative securities /
nork: Jarrow, Robert A.
Argitaratua: (2000)

Electronic Effects in Organic Chemistry
nork: Kirchner, Barbara
Argitaratua: (2020)

Quantitative source identification of dioxin-like PCBs in Yokohama, Japan, by temperature dependence of their atmospheric concentrations /
nork: Ogura, Isamu.