Enantioselective Synthesis of the Bottom Half of Chlorothricolide. 3. Studies of the Steric Directing Group Strategy for Stereocontrol in Intramolecular Diels-Alder Reactions

DOI: 10.1021/jo00003a049

Source and publish data:

Journal of Organic Chemistry p. 1192 - 1210 (1991)

Update date:2022-08-04

Topics:

Authors:

Roush, William R.

Kageyama, Masanori

Riva, Renata

Brown, Bradley B.

Warmus, Joseph S.

Moriarty, Kevin J.

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Article abstract of DOI:10.1021/jo00003a049

The intramolecular Diels-Alder reactions of a series of C(7)-alkoxy-substituted 2(E),8(Z),10(E)-undecatrienoates and trienals containing removable C(9)-Br or C(9)-SiMe3 substituents (11, 12, 13, 33, 42, 43, 44, 45) were studied as part of a programm direc

Full text of DOI:10.1021/jo00003a049

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