ChemInform Abstract: Cyclization Reactions of βγ‐Unsaturated Derivatives of Carbonic Acid. Part 11. Investigation of the Stereochemistry of the Cyclofunctionalization of βγ‐Unsaturated Carbamic Acid Esters.

Abstract The urethane (I) reacts with the sulfenyl chloride (II) to afford the racemic oxazolidines (III) with (5S,6R)‐ and (5R,6S)‐configuration.

Bibliographic Details
Published in:ChemInform
Main Authors: MUEHLSTAEDT, M. +, MEUSINGER, R., OLK, B., WEBER, L., WIDERA, R.
Format: Article in Journal/Newspaper
Language:English
Published: Wiley 1987
Subjects:
Carbonic acid
Online Access:http://dx.doi.org/10.1002/chin.198709169
http://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fchin.198709169
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fchin.198709169
https://onlinelibrary.wiley.com/doi/pdf/10.1002/chin.198709169
Description
Summary:Abstract The urethane (I) reacts with the sulfenyl chloride (II) to afford the racemic oxazolidines (III) with (5S,6R)‐ and (5R,6S)‐configuration.

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