Base-Induced Rearrangement of Perhydronaphthalene-1,4-diol Monosulfonate Esters to 11-Oxatricyclo[5.3.1.02,6]undecanes. Total Synthesis of Furanether B-Reference-Cited by-同舟云学术

Base-Induced Rearrangement of Perhydronaphthalene-1,4-diol Monosulfonate Esters to 11-Oxatricyclo[5.3.1.02,6]undecanes. Total Synthesis of Furanether B

Published:1998-01-01 Issue:1 Volume:63 Page:122-128
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Bell Roel P. L.¹,Sobolev Arkadij¹,Wijnberg Joannes B. P. A.¹,de Groot Aede¹

Affiliation:

1. Laboratory of Organic Chemistry, Agricultural University, Dreijenplein 8, 6703 HB Wageningen, The Netherlands

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo971545n

Reference40 articles.

1. Intramolecular alkoxide induced heterolysis of perhydronaphthalene-1,4-diol monosulfonate esters through orbital interactions over three carbon-carbon single bonds

2. Rearrangement vs Homofragmentation: Chemical Consequences of Different .sigma.-Relays on the Heterolysis of Sulfonate Esters Induced by Through-Bond Interactions

3. Chemical Consequences of Long-Range Orbital Interactions in Norbornane-Based 1,4-Diol Monosulfonate Esters

4. Base-induced and -directed rearrangements of 4-monotosylated perhydronaphthalene-1,4-diols. Synthesis of (.+-.)-5-epi-nardol

5. Total Synthesis of Dictamnol, a Trinor-Guaiane Type Sesquiterpene from the Roots of Dictamnus dasycarpus TURCZ.

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