INTRAMOLECULAR ADDITION OF AMINES TO CHIRAL VINYL SULFOXIDES, TOTAL SYNTHESIS OF (R)-(+)-CANADINE

DOI: 10.1016/S0040-4039(00)96613-9

Source and publish data:

Tetrahedron Letters p. 4737 - 4740 (1987)

Update date:2022-07-29

Topics:: Authors:

Pyne, Stephen G.

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Article abstract of DOI:10.1016/S0040-4039(00)96613-9

The intramolecular conjugate addition of an amine to the chiral vinyl sulfoxides 3 and 4 to give chiral isoquinolines 5 and 6 is reported.Isoquinoline 5 is converted to (R)-(+)-Canadine via an intramolecular Pummerer reaction.

Full text of DOI:10.1016/S0040-4039(00)96613-9

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Article Doi

INTRAMOLECULAR ADDITION OF AMINES TO CHIRAL VINYL SULFOXIDES, TOTAL SYNTHESIS OF (R)-(+)-CANADINE

DOI: 10.1016/S0040-4039(00)96613-9

Source and publish data:

Authors:

Article abstract of DOI:10.1016/S0040-4039(00)96613-9

Full text of DOI:10.1016/S0040-4039(00)96613-9

Products guided by the article

R&D Labs maybe for 116120-17-3

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Enhanced Glutathione Peroxidase Activity of Water-Soluble and Polyethylene Glycol-Supported Selenides, Related Spirodioxyselenuranes, and Pincer Selenuranes

Synthesis of novel 1,2,3,4-tetrahydrobenzo[c]-1,5-naphthyridines from pyrrolo[1,2-b]isoquinolines

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