Asymmetric synthesis of druglike six-membered spirooxindoles through an amino enyne catalysis

D. B. Ramachary; Chintalapudi Venkaiah; R. Madhavachary

doi:10.1021/ol401227q

Asymmetric synthesis of druglike six-membered spirooxindoles through an amino enyne catalysis

D. B. Ramachary^*
, Chintalapudi Venkaiah
, R. Madhavachary

^*Corresponding author for this work

School of Chemistry

Research output: Contribution to journal › Article (Academic Journal) › peer-review

99 Citations (Scopus)

Abstract

An effective reflexive-Michael (r-M) reaction has been disclosed to access drug-like six-membered spirooxindoles in good yields and excellent enantioselectivities by using an aminoenyne-catalysis.

Original language	English
Pages (from-to)	3042-3045
Number of pages	4
Journal	Organic Letters
Volume	15
Issue number	12
DOIs	https://doi.org/10.1021/ol401227q
Publication status	Published - 21 Jun 2013

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@article{409e1444130541fbbc4b2eee99bb2a1b,

title = "Asymmetric synthesis of druglike six-membered spirooxindoles through an amino enyne catalysis",

abstract = "An effective reflexive-Michael (r-M) reaction has been disclosed to access drug-like six-membered spirooxindoles in good yields and excellent enantioselectivities by using an aminoenyne-catalysis.",

author = "Ramachary, \{D. B.\} and Chintalapudi Venkaiah and R. Madhavachary",

year = "2013",

month = jun,

day = "21",

doi = "10.1021/ol401227q",

language = "English",

volume = "15",

pages = "3042--3045",

journal = "Organic Letters",

issn = "1523-7060",

publisher = "American Chemical Society",

number = "12",

}

TY - JOUR

T1 - Asymmetric synthesis of druglike six-membered spirooxindoles through an amino enyne catalysis

AU - Ramachary, D. B.

AU - Venkaiah, Chintalapudi

AU - Madhavachary, R.

PY - 2013/6/21

Y1 - 2013/6/21

N2 - An effective reflexive-Michael (r-M) reaction has been disclosed to access drug-like six-membered spirooxindoles in good yields and excellent enantioselectivities by using an aminoenyne-catalysis.

AB - An effective reflexive-Michael (r-M) reaction has been disclosed to access drug-like six-membered spirooxindoles in good yields and excellent enantioselectivities by using an aminoenyne-catalysis.

UR - https://www.scopus.com/pages/publications/84879346998

U2 - 10.1021/ol401227q

DO - 10.1021/ol401227q

M3 - Article (Academic Journal)

C2 - 23724824

AN - SCOPUS:84879346998

SN - 1523-7060

VL - 15

SP - 3042

EP - 3045

JO - Organic Letters

JF - Organic Letters

IS - 12

ER -

Asymmetric synthesis of druglike six-membered spirooxindoles through an amino enyne catalysis

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