Concise Synthesis of Spirocyclic, Bridged γ-Butyrolactones via Stereospecific, Dyotropic Rearrangements of β-Lactones Involving 1,2-Acyl and δ-Lactone Migrations-Reference-Cited by-同舟云学术

Concise Synthesis of Spirocyclic, Bridged γ-Butyrolactones via Stereospecific, Dyotropic Rearrangements of β-Lactones Involving 1,2-Acyl and δ-Lactone Migrations

Published:2008-07-16 Issue:32 Volume:130 Page:10478-10479
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Purohit Vikram C.¹,Matla Andrea S.¹,Romo Daniel¹

Affiliation:

1. Department of Chemistry, Texas A&M University, College Station, Texas 77842-3012

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja803579z

Reference29 articles.

1. Dyotropic Rearrangements, a New Class of Orbital-Symmetry Controlled Reactions. Type I

2. Mechanismus der Mutarotation von 5,6-Dibromcholestan

3. 196. Long-range effects in alicyclic systems. Part I. The rates of rearrangement of some steroidal dibromides

4. Stereoelectronic Effects on Type I 1,2-Dyotropic Rearrangements in Vicinal Dibromides

5. Reactions of β-lactones with Lewis acids: Ring enlargement versus β-elimination

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