Literature DB >> 10822567

Synthesis of four diastereomeric 3,5-dialkoxy-2,4-dimethylalkanals by a simple extension of the non-aldol aldol process to bis(propionates).

M E Jung1, W S Lee, D Sun.   

Abstract

[formula: see text] The synthesis of all four diastereomers of bis(propionates), 3,5-dialkoxy-2,4-dimethylalkanals, by non-aldol aldol chemistry is described. The epoxy alcohols (3, 4) were converted into the mesylates (9, 11) which were cleanly rearranged to the desired 3,5-bis(oxygenated)-2,4-dimethylalkanals (10, 12) in high yield. The epoxy mesylates (13, 16) gave the desired products (14, 17) in good yield on treatment with TMSOTf and a hindered base.

Entities:  

Mesh:

Substances:

Year:  1999        PMID: 10822567     DOI: 10.1021/ol990619+

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


  4 in total

1.  Computational elucidation of the origins of reactivity and selectivity in non-aldol aldol rearrangements of cyclic epoxides.

Authors:  Hao Wang; K N Houk; Damian A Allen; Michael E Jung
Journal:  Org Lett       Date:  2011-05-13       Impact factor: 6.005

2.  Total synthesis of auripyrone B using a non-aldol aldol-cuprate opening process.

Authors:  Michael E Jung; Manon Chaumontet; Ramin Salehi-Rad
Journal:  Org Lett       Date:  2010-06-18       Impact factor: 6.005

3.  Asymmetric synthesis of anti-aldol segments via a nonaldol route: synthetic applications to statines and (-)-tetrahydrolipstatin.

Authors:  Arun K Ghosh; Khriesto Shurrush; Sarang Kulkarni
Journal:  J Org Chem       Date:  2009-06-19       Impact factor: 4.354

Review 4.  Total Syntheses of Pladienolide-Derived Spliceosome Modulators.

Authors:  Jaehoon Sim; Eunbin Jang; Hyun Jin Kim; Hongjun Jeon
Journal:  Molecules       Date:  2021-09-30       Impact factor: 4.411

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.