Literature DB >> 15554251

Functional divergency oriented synthesis of azoninones as the key intermediates for bioactive indolizidine alkaloids analogs.

Jae-Kyung Jung1, Nam-Song Choi, Young-Ger Suh.   

Abstract

A functional divergency oriented synthetic approach to the azoninone (9-membered lactams), key intermediate for the indolizidine alkaloids library, using amide enolate induced aza-Claisen rearrangement has been achieved.

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Year:  2004        PMID： 15554251     DOI： 10.1007/bf02975418

Source DB:  PubMed          Journal:  Arch Pharm Res        ISSN： 0253-6269            Impact factor:   4.946


  2 in total

1.  Unexpected Rearrangement of N-Allyl-2-phenyl-4,5-Dihydrooxazole-4-Carboxamides to Construct Aza-Quaternary Carbon Centers.

Authors:  Goyeong Choi; Seoyoung Jo; Juyeon Mun; Yonguk Jeong; Seok-Ho Kim; Jong-Wha Jung
Journal:  Molecules       Date:  2019-12-08       Impact factor: 4.411

2.  Asymmetric Synthesis of (-)-6-Desmethyl-Fluvirucinine A₁ via Conformationally-Controlled Diastereoselective Lactam-Ring Expansions.

Authors:  Hyunyoung Moon; Hojong Yoon; Changjin Lim; Jaebong Jang; Jong-Jae Yi; Jae Kyun Lee; Jeeyeon Lee; Younghwa Na; Woo Sung Son; Seok-Ho Kim; Young-Ger Suh
Journal:  Molecules       Date:  2018-09-14       Impact factor: 4.411
  2 in total

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