1-Oxaspiro[4.4]nonan-6-ones. Synthetic Access via Oxonium Ion Technology, Optical Resolution, and Conversion into Enantiopure Spirocyclic α,β-Butenolides-Reference-Cited by-同舟云学术

1-Oxaspiro[4.4]nonan-6-ones. Synthetic Access via Oxonium Ion Technology, Optical Resolution, and Conversion into Enantiopure Spirocyclic α,β-Butenolides

Published:2001-03-22 Issue:8 Volume:66 Page:2828-2834
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Paquette Leo A.¹,Owen Dafydd R.¹,Bibart Richard Todd¹,Seekamp Christopher K.¹,Kahane Alexandra L.¹,Lanter James C.¹,Corral Miriam Alvarez¹

Affiliation:

1. Evans Chemical Laboratories, The Ohio State University, Columbus, Ohio 43210

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo010026o

Reference46 articles.

1. Response of 2-Lithio-4,5-dihydrofuran — Ketone Adducts to Acid Catalysis

2. The pinacol rearrangement

3. Regio- and stereochemical course of the ring expansion of bridged bicyclic ketones to spirocyclic .alpha.-keto tetrahydrofurans.

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