Stereocontrolled Synthesis of Cyclic Ethers by Intramolecular Hetero-Michael Addition. 6. A Computational Study of the Annelation to 2,3-Disubstituted Tetrahydropyrans-Reference-Cited by-同舟云学术

Stereocontrolled Synthesis of Cyclic Ethers by Intramolecular Hetero-Michael Addition. 6. A Computational Study of the Annelation to 2,3-Disubstituted Tetrahydropyrans

Published:1997-07-01 Issue:14 Volume:62 Page:4584-4590
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Ramírez Miguel A.¹,Padrón José M.¹,Palazón José M.¹,Martín Víctor S.¹

Affiliation:

1. Instituto Universitario de Bio-Orgánica “Antonio González”, Universidad de La Laguna, Carretera de La Esperanza, 2, 38206 La Laguna, Tenerife, Spain

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo961925t

Reference57 articles.

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2. 24. A general stereoselective synthesis of olefins

3. Asymmetric Induction. A Model for Additions to Carbonyls Directly Bonded to Asymmetric Carbons

4. Torsional strain involving partial bonds. The stereochemistry of the lithium aluminium hydride reduction of some simple open-chain ketones

5. Torsional strain involving partial bonds. The steric course of the reaction between allyl magnesium bromide and 4-t-butyl-cyclohexanone

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