Generation of the new quirogane skeleton by a vinylogous retro-Michael type rearrangement of longipinene derivatives-Reference-Cited by-同舟云学术

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Generation of the new quirogane skeleton by a vinylogous retro-Michael type rearrangement of longipinene derivatives

Published:2001-08 Issue:34 Volume:57 Page:7269-7275
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Román Luisa U,Rebeca Morales N,Hernández Juan D,Cerda-Garcı́a-Rojas Carlos M,Gerardo Zepeda L,Flores-Sandoval César A,Joseph-Nathan Pedro

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference16 articles.

1. Studies in sesquiterpenes-lx reversion of longipinane to himachalane system : revision of structure of isocentdarol

2. Wagner-Meerwein rearrangements of longipinane derivatives

3. Molecular Rearrangements in the Longipinene Series

4. Molecular Rearrangement of Rastevione Mesylate into Arteagane Derivatives

5. Mechanistic Studies of the Longipinane to Arteagane Rearrangement

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3. Novel Sesquiterpenoid Skeletons by Wagner–Meerwein Rearrangements of Longipinane-9,13-diol-1-one Derivatives;Journal of Natural Products;2021-03-18

4. Synthesis of 2-chromanone-fused [3.2.0] bicycles through a phosphine-mediated tandem [3 + 2] cyclization/intramolecular Wittig reaction;Organic Chemistry Frontiers;2021

5. Novel Sesquiterpene Skeletons by Multiple Wagner–Meerwein Rearrangements of a Longipinane-1,9-diol Derivative;Journal of Natural Products;2019-11-27

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