3-exo,3'-exo-(1R,1'R)-Bithiocamphor - a Versatile Source for Functionally Different 3,3'-Bibornane Derivatives - I. Ring-Closure Reactions and Prototropic Rearrangements

DOI: 10.1016/0040-4020(95)00852-Y

Source and publish data:

Tetrahedron p. 13247 - 13260 (1995)

Update date:2022-09-26

Topics:

Authors:

Schroth, Werner

Hintzsche, Ekkehard

Spitzner, Roland

Stroehl, Dieter

Sieler, Joachim

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Article abstract of DOI:10.1016/0040-4020(95)00852-Y

The title compound 3, derived from (+)-camphor, allows preparatively useful conversions to be carried out at the 3,3'-bibornane skeleton.The reactions are characterized by steric factors.Despite the increasing steric strain in the bicyclic units, ring-clo

Full text of DOI:10.1016/0040-4020(95)00852-Y

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