Literature DB >> 15255693

Stereoselective iodocyclization of 3-acylamino-2-methylene alkanoates: synthesis of analogues of N-benzoyl-syn-phenylisoserine.

Roberta Galeazzi1, Gianluca Martelli, Giovanna Mobbili, Mario Orena, Samuele Rinaldi.   

Abstract

[reaction: see text] A convenient approach to racemic analogues of N-benzoyl-syn-phenylisoserine was realized via the stereoselective iodocyclization of amides obtained from Baylis-Hillman adducts.

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Year:  2004        PMID： 15255693     DOI： 10.1021/ol049146j

Source DB:  PubMed          Journal:  Org Lett        ISSN： 1523-7052            Impact factor:   6.005


  4 in total

1.  Enzymatic deprotection of the cephalosporin 3'-acetoxy group using Candida antarctica lipase B.

Authors:  Leslie D Patterson; Marvin J Miller
Journal:  J Org Chem       Date:  2010-02-19       Impact factor: 4.354

2.  Enantiopure derivatives of aza-Baylis-Hillman adducts by subsequent SN'-SN' reactions of acylcarbamates bearing a chiral auxiliary.

Authors:  Gianluca Martelli; Eleonora Marcucci; Mario Orena; Samuele Rinaldi
Journal:  Molecules       Date:  2009-07-30       Impact factor: 4.411

3.  Fluorocyclisation via I(I)/I(III) catalysis: a concise route to fluorinated oxazolines.

Authors:  Felix Scheidt; Christian Thiehoff; Gülay Yilmaz; Stephanie Meyer; Constantin G Daniliuc; Gerald Kehr; Ryan Gilmour
Journal:  Beilstein J Org Chem       Date:  2018-05-09       Impact factor: 2.883

4.  Asymmetric synthesis of multifunctional aryl allyl ethers by nucleophilic catalysis.

Authors:  Shuai Zhao; Lei Jin; Zhi-Li Chen; Xue Rui; Jia-Yi He; Ran Xia; Ke Chen; Xiang-Xiang Chen; Zi-Jian Yin; Xin Chen
Journal:  RSC Adv       Date:  2019-04-12       Impact factor: 4.036
  4 in total

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