Addition reactions of allyl stannanes to an indolo[2',3':3,4]pyrido[1,2-b]isoquinoline imminium salt

DOI: 10.1002/jhet.5570370510

Source and publish data:

Journal of Heterocyclic Chemistry p. 1081 - 1087 (2000)

Update date:2022-08-04

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Authors:

Unangst Unangst

Bratton Bratton

Connor Connor

Roth Roth

Rubin Rubin

Trivedi Trivedi

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Article abstract of DOI:10.1002/jhet.5570370510

The addition of organometallic reagents to the 13b-position of the indolo[2',3':3,4]pyrido[1,2-b]isoquinoline imminium salt 4 is described. Reaction of 4 with tetraallyl tin in 2-methoxyethanol gave the allyl adduct 7 in moderate yield. Further elaboratio

Full text of DOI:10.1002/jhet.5570370510

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Product name:[4aS-(2E,4aα,13β,14aβ)]-13b-allyl-3-benzylidene-3,4,4a,5,7,8,13,13b,14,14a-decahydro-1H-indolo[2',3':3,4]pyrido[1,2-b]isoquinolin-2-one

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