Results 61 to 70 of about 2,138 (143)
We report herein two stereocomplementary approaches to erythro/trans and threo/cis vicinal amino diol subunits containing 2-pyrrolidinones (9 and 10) starting from the known enamides 7, easily available from malimides.
Jian-Liang Ye (1883158) +3 more
core +2 more sources
A versatile and highly diastereoselective four-step approach to (4S,5R)-N-benzyl-4-benzyloxy-5-(alpha-hydroxyalkyl)-2-pyrrolidinones 2, which starts from readily available (S)-N,O-dibenzylmalimide (5), is reported.
Zhang, Pan-Yuan +8 more
core +1 more source
5-trans-Substituted 2-pyrrolidinones 6a, 6c and 6d and 5,5-disubstituted 2-pyrrolidinones 6e-k were regio- and diastereoselectively formed through the addition of organolithium species to imides 1a,b derived from malic acid, followed by addition of ...
Pilli, RA, Schuch, CM
core +1 more source
Controlled hydrolysis of aryltellurium trichlorides using 2-pyrrolidinones: Isolation and structural characterization of monomeric aryltellurium(IV ...
R Butcher (12222107) +4 more
core
Treatment of N-allyl-N¢,N¢-dimethyl-2,2-dichlorohydrazides with CuCl/TMEDA in ethyl acetate35is a mild and easy method for preparing N-(dimethylamino)-2-pyrrolidinones.
Parsons AF +3 more
core +1 more source
The halogen atom transfer radical cyclization of a N-allyl-N-benzyl-2,2-dihaloamides to 2-pyrrolidinones has been carried out in high yields under mild conditions, in a reaction promoted by CuCl-TMEDA or Fe-0-FeCl3 in acetonitrile or N,N ...
Franco Ghelfi +9 more
core +1 more source
Enols are used for the first time in a condensation with aldehydes and isocyanides to selectively give three- or pseudo-four-component adducts, depending on the reaction conditions. These new transformations have proven to be a convenient alternative for
Carlos F. Marcos (1580926) +3 more
core +1 more source
Synthesis of new optically active 2-pyrrolidinones.
A new class of optically active 2-pyrrolidinones was synthesized, starting from S-pyroglutamic acid, a well known natural chiral synthon. The synthetic design followed led to the insertion of various substituents at positions 1 and 5 of the 2 ...
T. Mavromoustakos +2 more
core
Studies on the Asymmetric Synthesis of cis-5-Alkyl-4-hydroxy-2–pyrrolidinones and Studies on the New Method for Reduction of Amide [PDF]
本论文包含以下各自独立的三方面内容:1,顺式-4-羟基-5-烷基-2-吡咯烷酮4的不对称合成研究;2,CytosporoneB类单羟基衍生物的合成;3,酰胺还原新方法研究。 一、顺式-4-羟基-5-烷基-2-吡咯烷酮4的不对称合成研究: 很多天然产物中含有顺式-4-羟基-5-烷基-2-吡咯烷酮亚结构,它们大多数具有很好的生理活性。此结构开环后得到的γ-氨基-β-羟基酸是一类特种氨基酸,它们是许多具有重要生理活性天然产物的结构单元。因此,关于此类化合物的研究一直吸引着人们的兴趣 ...
向少华
core
Synthesis and structural investigation of some 1,4-disubstituted-2-pyrrolidinones
Kristina Brokaite +2 more
doaj +1 more source

