Rearrangement of isodigitoxigenin

George Pettit; J. C. Knight; T. R. Kasturi

doi:10.1039/C19670000688

Rearrangement of isodigitoxigenin

George Pettit, J. C. Knight, T. R. Kasturi

Research output: Contribution to journal › Article › peer-review

Original language	English (US)
Pages (from-to)	688-689
Number of pages	2
Journal	Chemical Communications (London)
Issue number	14
DOIs	https://doi.org/10.1039/C19670000688
State	Published - 1967

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Chemistry(all)

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@article{b51984d789ac48ac9618a02e2c3d62a6,

title = "Rearrangement of isodigitoxigenin",

author = "George Pettit and Knight, {J. C.} and Kasturi, {T. R.}",

note = "Funding Information: Lactone (11) (0.42 g.) was subjected to alcoholysis using toluene-p-sulphonic acid (0.0 1 g.) in refluxing t Previous Paper : see ref 1. This investigation was supported by Public Health Service Grants from the National All new compounds have been adequately characterized by elemental analyses and 'H n.m.r. measurements Optical rotations were measured Acetylation reactions were conducted employing 1 : 1 acetic anhydride-pyridine at room Cancer Institute. (Varian A-60 spectrometer with CDC1, as solvent and Me,Si as internal standard). in chloroform solution. temperature.CHEMICAL COMMUNICATIONS, 1967 689 RO{\textquoteright} - - (I) a; R=H, b; R=Ac (26 hr.) methanol-water.l Following acetylation, acetals (Va) [0.26 g., m.p. 103-105”, lH n.m.r. Copyright: Copyright 2007 Elsevier B.V., All rights reserved.",

year = "1967",

doi = "10.1039/C19670000688",

language = "English (US)",

pages = "688--689",

journal = "Chemical Communications (London)",

issn = "0009-241X",

number = "14",

}

TY - JOUR

T1 - Rearrangement of isodigitoxigenin

AU - Pettit, George

AU - Knight, J. C.

AU - Kasturi, T. R.

N1 - Funding Information: Lactone (11) (0.42 g.) was subjected to alcoholysis using toluene-p-sulphonic acid (0.0 1 g.) in refluxing t Previous Paper : see ref 1. This investigation was supported by Public Health Service Grants from the National All new compounds have been adequately characterized by elemental analyses and 'H n.m.r. measurements Optical rotations were measured Acetylation reactions were conducted employing 1 : 1 acetic anhydride-pyridine at room Cancer Institute. (Varian A-60 spectrometer with CDC1, as solvent and Me,Si as internal standard). in chloroform solution. temperature.CHEMICAL COMMUNICATIONS, 1967 689 RO’ - - (I) a; R=H, b; R=Ac (26 hr.) methanol-water.l Following acetylation, acetals (Va) [0.26 g., m.p. 103-105”, lH n.m.r. Copyright: Copyright 2007 Elsevier B.V., All rights reserved.

PY - 1967

Y1 - 1967

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UR - http://www.scopus.com/inward/citedby.url?scp=37049117675&partnerID=8YFLogxK

U2 - 10.1039/C19670000688

DO - 10.1039/C19670000688

M3 - Article

AN - SCOPUS:37049117675

SN - 0009-241X

SP - 688

EP - 689

JO - Chemical Communications (London)

JF - Chemical Communications (London)

IS - 14

ER -

Rearrangement of isodigitoxigenin

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