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Second approach to the construction of a pentacyclic ring system for neosurugatoxin

DOI: 10.1248/cpb.40.1110

Source and publish data:

Chemical and Pharmaceutical Bulletin p. 1110 - 1115 (1992)

Update date:2022-08-04

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Authors:

OkadaOkada

MizunoMizuno

TaninoTanino

KakoiKakoi

InoueInoue

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Article abstract of DOI:10.1248/cpb.40.1110

The Diels-Alder adduct obtained from (E)-6-bromo-3-ethoxycarbonylmethylene-2-oxoindoline and trans-1,3-pentadiene was successfully transformed into the diacetate of the aglycone of neosurugatoxin, which is the key intermediate in our first total synthesis

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Full text of DOI:10.1248/cpb.40.1110

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Products guided by the article

Product name:2-(methylsulfonyl)ethyl 6'-bromo-1',2'-dihydro-5-methyl-3-<<<5-nitro-2,6-bis(phenylmethoxy)-4-pyrimidinyl>amino>methyl>-2'-oxospiro<3-cyclopentene-1,3'-<3H>indole>-2-carboxylate

Cas No:123973-57-9

123973-57-9

R&D Labs maybe for 123973-57-9

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