نتایج جستجو برای: 2 propenyl moiety

تعداد نتایج: 2535721  

Journal: :The Journal of the Society of Chemical Industry, Japan 1960

2000
S. Krompiec M. Antoszczyszyn T. Bieg

The allyl and propenyl ethers of diols and polyols have recently attracted increasing attention as monomers and comonomers [1–2]. Most convenient method of the preparation of propenyl ethers consists in isomerization of the corresponding, readily available allyl ethers. Moreover, this isomerization is a key step of deprotection of hydroxyl group, protected as allyl ether [3,4]. Particularly con...

Journal: :Chemical & pharmaceutical bulletin 2002
Akito Yasuhara Naoyuki Suzuki Takao Sakamoto

Furostifoline, a furo[3,2-a]carbazole alkaloid, was synthesized in 10% overall yield in four steps from 2-acetyl-3-bromofuran. The key step of this synthesis was the 2-substituted indole formation with tetrabutylammonium fluoride (TBAF) from 2-(2-propenyl)-3-((2-ethoxycarbonylamino)phenylethynyl)furan, which was easily prepared from ethyl 2-ethynylphenylcarbamate with 3-bromo-2-(2-propenyl)fura...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1999
H Mao N C Schnetz-Boutaud J P Weisenseel L J Marnett M P Stone

The primary DNA lesion induced by malondialdehyde, a byproduct of lipid peroxidation and prostaglandin synthesis, is 3-(2'-deoxy-beta-D-erythro-pentofuranosyl)-pyrimido[1, 2-a]purin-10(3H)-one (M1G). When placed opposite cytosine (underlined) at neutral pH in either the d(GGTMTCCG).d(CGGACACC) or d(ATCGCMCGGCATG). d(CATGCCGCGCGAT) duplexes, M1G spontaneously and quantitatively converts to the r...

Journal: :Bioorganic & medicinal chemistry 2012
L W Lawrence Woo Bertrand Leblond Atul Purohit Barry V L Potter

Estrone sulfamate (EMATE) is a potent irreversible inhibitor of steroid sulfatase (STS). In order to further expand SAR, the compound was substituted at the 2- and/or 4-positions and its 17-carbonyl group was also removed. The following general order of potency against STS in two in vitro systems is observed for the derivatives: The 4-NO(2) > 2-halogens, 2-cyano > EMATE (unsubstituted)>17-deoxy...

Journal: :Inorganics (Basel) 2022

The efficient regio- and stereoselective syntheses of (Z,Z)-bis(3-amino-3-oxo-1-propenyl) selenides diselenides in high yields based on the nucleophilic addition sodium selenide to 2-propynamides diselenide 3-(trimethylsilyl)-2-propynamides have been developed. first examples a selenium-centered nucleophile with terminal triple bond anion carried out. Bis(3-amino-3-oxo-1-propenyl) are novel fam...

Journal: :PLoS ONE 2007
Gordon V. Louie Thomas J. Baiga Marianne E. Bowman Takao Koeduka John H. Taylor Snejina M. Spassova Eran Pichersky Joseph P. Noel

Phenylpropenes, a large group of plant volatile compounds that serve in multiple roles in defense and pollinator attraction, contain a propenyl side chain. Eugenol synthase (EGS) catalyzes the reductive displacement of acetate from the propenyl side chain of the substrate coniferyl acetate to produce the allyl-phenylpropene eugenol. We report here the structure determination of EGS from basil (...

Journal: :Environmental Health Perspectives 1995
Gordon V. Louie Thomas J. Baiga Marianne E. Bowman Takao Koeduka John H. Taylor Snejina M. Spassova Eran Pichersky Joseph P. Noel

Phenylpropenes, a large group of plant volatile compounds that serve in multiple roles in defense and pollinator attraction, contain a propenyl side chain. Eugenol synthase (EGS) catalyzes the reductive displacement of acetate from the propenyl side chain of the substrate coniferyl acetate to produce the allyl-phenylpropene eugenol. We report here the structure determination of EGS from basil (...

Journal: :Organic & biomolecular chemistry 2009
Jun-Ming Mo Yang-Guang Ma Ying Cheng

2-(2-Alkoxycarbonyl-1-arylamino-1-propenyl)benzimidazolium and 5-(2-alkoxycarbonyl-1-arylamino-1-propenyl)triazolium salts were synthesized in good yields from the reaction of benzimidazole and triazole carbenes with ketenimines. Upon treatment with a base, both salts were converted into novel 1,3-dipoles which underwent [3+2] cycloaddition reactions with electron-deficient alkynes and allenes ...

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