Literature DB >> 17956115

Total synthesis of amaminol A: establishment of the absolute stereochemistry.

Esa T T Kumpulainen1, Ari M P Koskinen, Kari Rissanen.   

Abstract

The first synthetic route to amaminol A with use of an organocatalytic intramolecular Diels-Alder reaction is reported. The absolute stereochemistry is proven with a crystallographic image of a cyclic carbamate of amaminol A.

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Year:  2007        PMID： 17956115     DOI： 10.1021/ol7022856

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


  2 in total

1.  Solid-phase synthesis of cyclic hexapeptides wollamides A, B and desotamide B.

Authors:  Lissa S Tsutsumi; Ghee T Tan; Dianqing Sun
Journal:  Tetrahedron Lett       Date:  2017-05-25       Impact factor: 2.415

Review 2.  Advances in the Asymmetric Total Synthesis of Natural Products Using Chiral Secondary Amine Catalyzed Reactions of α,β-Unsaturated Aldehydes.

Authors:  Zhonglei Wang
Journal:  Molecules       Date:  2019-09-19       Impact factor: 4.411
  2 in total

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