Facile Method for Stereoselective Synthesis of New Chiral (1R,4aR,8aR)‐1,3,4,4a,5,7,8,8a‐Octahydro‐2‐methylene‐naphthalene‐6‐one‐1‐propanenitrile, an Important Precursor of Solanapyrones-Reference-Cited by-同舟云学术

Facile Method for Stereoselective Synthesis of New Chiral (1R,4aR,8aR)‐1,3,4,4a,5,7,8,8a‐Octahydro‐2‐methylene‐naphthalene‐6‐one‐1‐propanenitrile, an Important Precursor of Solanapyrones

Published:2006-02-01 Issue:2 Volume:36 Page:237-248
ISSN:0039-7911
Container-title:Synthetic Communications
language:en
Short-container-title:Synthetic Communications

Author:

Shi Haijian¹

Affiliation:

1. a College of Chemistry and Chemical Engineering, Key Laboratory of Material‐Oriented Chemical Engineering of Jiangsu Provience , Nanjing University of Technology , Nanjing , China

Publisher

Informa UK Limited

Subject

Organic Chemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/00397910500334611

Reference31 articles.

1. First Total Syntheses of the Phytotoxins Solanapyrones D and E via the Domino Michael Protocol

2. The First Total Synthesis of (−)-Solanapyrone E Based on Domino Michael Strategy

3. Structure and absolute configuration of solanapyrone D: a new clue to the occurrence of biological Diels–Alder reactions

4. Synthesis of (±)-solanapyrones A and B

5. Involvement of Diels–Alder reactions in the biosynthesis of secondary natural products: the late stage of the biosynthesis of the phytotoxins solanapyrones

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