[3,3] Sigmatropic rearrangement of allylic alcohols with ethyl β,β-diethoxyacrylate: Regiospecific synthesis of substituted allylmalonates-Reference-Cited by-同舟云学术

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[3,3] Sigmatropic rearrangement of allylic alcohols with ethyl β,β-diethoxyacrylate: Regiospecific synthesis of substituted allylmalonates

Published:1985 Issue:51 Volume:26 Page:6261-6264
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Raucher Stanley,Chi Ki-Whan,Jones David S.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference34 articles.

1. Stereo- and regiochemistry of the Claisen rearrangement: applications to natural products synthesis

2. The Claisen Rearrangement in Organic Synthesis; 1967 to January 1977

3. Simple stereoselective version of the Claisen rearrangement leading to trans-trisubstituted olefinic bonds. Synthesis of squalene

4. Indole alkaloid synthesis via Claisen rearrangement. Total synthesis of secodine

Cited by 12 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Synthesis of the tricyclic core of manzamine A;Organic & Biomolecular Chemistry;2015

2. Ethyl 3,3-diethoxyacrylate;Fieser and Fieser's Reagents for Organic Synthesis;2006-12-15

3. An approach to the synthesis of phomactins using a Wittig rearrangement;Arkivoc;2003-01-06

4. 2,4,6-Trimethylbenzoic Acid;Encyclopedia of Reagents for Organic Synthesis;2001-04-15

5. Ethyl 3,3-Diethoxyacrylate;Encyclopedia of Reagents for Organic Synthesis;2001-04-15

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