Literature DB >> 17551632

An efficient method for the synthesis of enol ethers and enecarbamates. Total syntheses of isoindolobenzazepine alkaloids, lennoxamine and chilenine.

Haruhiko Fuwa1, Makoto Sasaki.   

Abstract

An efficient method for the synthesis of enol ethers and enecarbamates has been developed based on catalytic hydrosilane reduction of alpha-phosphonoxy enol ethers and alpha-phosphonoxy enecarbamates. This method has been applied to the total syntheses of two isoindolobenzazepine alkaloids, lennoxamine and chilenine.

Entities:  

Mesh：

Substances：

Year:  2007        PMID： 17551632     DOI： 10.1039/b706087d

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN： 1477-0520            Impact factor:   3.876


  3 in total

1.  A ring expansion strategy towards diverse azaheterocycles.

Authors:  Ruirui Li; Bo Li; Hongpeng Zhang; Cheng-Wei Ju; Ying Qin; Xiao-Song Xue; Dongbing Zhao
Journal:  Nat Chem       Date:  2021-07-19       Impact factor: 24.427

2.  Efficient synthesis of a (Z)-3-methyleneisoindolin-1-one library using Cu(OAc)₂•H₂O/DBU under microwave irradiation.

Authors:  Li Zhang; Yongliang Zhang; Xin Wang; Jingkang Shen
Journal:  Molecules       Date:  2013-01-04       Impact factor: 4.411

3.  Facile synthesis of α-alkoxymethyltriphenylphosphonium iodides: new application of PPh3/I2.

Authors:  Humaira Yasmeen Gondal; Zain Maqsood Cheema; Javid Hussain Zaidi; Sammer Yousuf; M Iqbal Choudhary
Journal:  Chem Cent J       Date:  2018-05-17       Impact factor: 4.215
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.