Literature DB >> 16468739

General method for synthesizing pyranoid glycals. A new route to allal and gulal derivatives.

Omar Boutureira1, Miguel Angel Rodríguez, M Isabel Matheu, Yolanda Díaz, Sergio Castillón.   

Abstract

[reaction: see text] Pyranoid glycals of all configurations can be obtained from pentoses through an olefination-cyclization-elimination sequence. The elimination can be carried out with excellent yields under radical conditions or by using common reductive reagents such as Zn/Cu, TiCl(4)/LiAlH(4), or lithium naphthalenide. The proposed method is appropriate for the synthesis of glycals with allo or gulo configurations because the cyclization step is more efficient for these substrates.

Entities:  

Year:  2006        PMID: 16468739     DOI: 10.1021/ol052866l

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


  3 in total

1.  Highly reactive 2-deoxy-2-iodo-d-allo and d-gulo pyranosyl sulfoxide donors ensure β-stereoselective glycosylations with steroidal aglycones.

Authors:  Jordi Mestre; David Collado; David Benito-Alifonso; Miguel A Rodríguez; M Isabel Matheu; Yolanda Díaz; Sergio Castillón; Omar Boutureira
Journal:  RSC Adv       Date:  2018-08-24       Impact factor: 4.036

2.  P(v) intermediate-mediated E1cB elimination for the synthesis of glycals.

Authors:  Fen Liu; Haiyang Huang; Longgen Sun; Zeen Yan; Xiao Tan; Jing Li; Xinyue Luo; Haixin Ding; Qiang Xiao
Journal:  Chem Sci       Date:  2022-04-22       Impact factor: 9.969

3.  The convergent total synthesis and antibacterial profile of the natural product streptothricin F.

Authors:  Matthew G Dowgiallo; Brandon C Miller; Mintesinot Kassu; Kenneth P Smith; Andrew D Fetigan; Jason J Guo; James E Kirby; Roman Manetsch
Journal:  Chem Sci       Date:  2022-02-25       Impact factor: 9.969

  3 in total

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