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Combining Organocatalyzed Aldolization and Reductive Amination: An Efficient Reaction Sequence for the Synthesis of Iminosugars
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- المصدر:
European Journal of Organic Chemistry
- نوع التسجيلة:
Electronic Resource
- الدخول الالكتروني :
info:eu-repo/grantAgreement/MESTD/inst-2020/200168/RS
Serbian Academyof Sciences and Arts, Project No F193.
- معلومة اضافية
- Publisher Information:
Wiley 2021
- Added Details:
Ferjančić, Zorana
Saičić, Radomir
- نبذة مختصرة :
Over the past two decades, organocatalytic aldol reaction emerged as a powerful method for the enantioselective carbon–carbon bond formation, often offering more efficient, economical and environmentally friendly synthesis of chiral molecules. On the other hand, reductive amination is one of the most important reactions in synthesis of biologically active compounds and drug candidates. Coupling these two reactions results in a powerful combination that allows for a rapid, stereoselective access to substituted, highly functionalized five- and six-membered N-heterocycles. This minireview illustrates the applicability of this approach as the key feature in syntheses of various iminosugars – a class of polyhydroxylated alkaloids with a range of interesting biological activities and high pharmacological potential.
- الموضوع:
- Note:
European Journal of Organic Chemistry
- Other Numbers:
RSPST oai:cherry.chem.bg.ac.rs:123456789/4576
1434-193X
https://onlinelibrary.wiley.com/doi/abs/10.1002/ejoc.202100398
https://cherry.chem.bg.ac.rs/handle/123456789/4576
000664610800012
10.1002/ejoc.202100398
2-s2.0-85108284643
1269080239
- Contributing Source:
UIVERSITY OF BELGRADE
From OAIster®, provided by the OCLC Cooperative.
- الرقم المعرف:
edsoai.on1269080239
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