نتایج جستجو برای: ring substitution

تعداد نتایج: 177743  

Journal: :علوم 0

in this note we introduce the notion of weak mccoy rings as a generalization of mccoy rings, and investigate their properties. also we show that, if is a semi-commutative ring, then is weak mccoy if and only if is weak mccoy.

Journal: :The Biochemical journal 2010
Noriyo Mitome Sakurako Ono Hiroki Sato Toshiharu Suzuki Nobuhito Sone Masasuke Yoshida

In F(o)F(1) (F(o)F(1)-ATP synthase), proton translocation through F(o) drives rotation of the oligomer ring of F(o)-c subunits (c-ring) relative to F(o)-a. Previous reports have indicated that a conserved arginine residue in F(o)-a plays a critical role in the proton transfer at the F(o)-a/c-ring interface. Indeed, we show in the present study that thermophilic F(o)F(1s) with substitution of th...

Journal: :SIAM Journal on Applied Algebra and Geometry 2021

We provide a reduction of the Ring-LWE problem to problems in subrings, presence samples restricted form (i.e., $(a,b)$ such that $a$ is multiplicative coset subring). To create and exploit samples, we propose Ring-BKW, version Blum--Kalai--Wasserman (BKW) algorithm which respects ring structure. Off-the-shelf BKW dimension (including coded-BKW sieving) can be used for phase. Its primary advant...

2015
Christina Schjoeth-Eskesen Paul Robert Hansen Andreas Kjaer Nic Gillings

Aziridines can undergo a range of ring-opening reactions with nucleophiles. The regio- and stereochemistry of the products depend on the substituents on the aziridine. Aziridine ring-opening reactions have rarely been used in radiosynthesis. Herein we report the ring opening of activated aziridine-2-carboxylates with [(18)F]fluoride. The aziridine was activated for nucleophilic attack by substi...

Journal: :Bioscience, biotechnology, and biochemistry 2003
Mitsuru Ito Hideshi Okui Harumi Nakagawa Shigeru Mio Ayako Kinoshita Takashi Obayashi Takako Miura Junko Nagai Shinji Yokoi Reiji Ichinose Keiji Tanaka Seiichiro Kodama Toshiaki Iwasaki Takaaki Miyake Miho Takashio Jun Iwabuchi

A series of 5-spirocyclohexyl-3-(2,6-dimethylphenyl)-1,5-dihydro-2H-pyrrol-2-one derivatives (3) with various substituents on the spirocyclohexyl ring was synthesized and evaluated for its insecticidal activity against the aphid, Myzus persicae. Substituents at the 1- and 4-positions of the dihydropyrrole ring were also varied to optimize the activity. An investigation of the structure-activity...

Journal: :Molecules 2012
Saioa Ancizu Nerea Castrillo Silvia Pérez-Silanes Ignacio Aldana Antonio Monge Philippe Delagrange Daniel-Henry Caignard Silvia Galiano

Ever since the idea arose that melatonin might promote sleep and resynchronize circadian rhythms, many research groups have centered their efforts on obtaining new melatonin receptor ligands whose pharmacophores include an aliphatic chain of variable length united to an N-alkylamide and a methoxy group (or a bioisostere), linked to a central ring. Substitution of the indole ring found in melato...

2012
Xiangdong Zhang Junwei Ye Weitao Gong Yuan Lin Guiling Ning

The racemic title compound, C(54)H(38)O(2), consists of two C-linked penta-leno[1,2,3-ij]naphthalenone moieties, the crowded aryl ring substitution on the cyclo-pentane rings forcing the two segments to assume a conformation which has pseudo-twofold rotational symmetry, with a dihedral angle between the naphthalene substituent groups of 55.30 (8)°. In each segment, the two phenyl rings have dif...

2013
Jun Tan Chul-Ho Kim Hyun-Joo Lee Jing Chen Qing Zhong Chen In-Ho Jeon

BACKGROUND Current examination methods to assess the anatomical variations of flexor digitorum superficialis (FDS) tendon in the little finger necessitate a strong external force applied by the examiner and cause false negatives. A new examination method was designed to detect the variations more accurately. METHODS We examined the little fingers of 220 adult hands (110 subjects) by 2 methods...

Journal: :Asian Journal of Organic Chemistry 2021

An N-heterocyclic carbene-catalyzed [3+3] cycloaddition reaction of acylthioureas with ynals is reported. Both N atoms in the thiourea substrate are activated as nucleophiles and incorporated inside ring system product. Pyrimidinthione derivatives bearing various substituents substitution patterns afforded products moderate to good yields.

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