First stereoselective total synthesis of (−)-Inohanalactone
Publication type: Journal Article
Publication date: 2020-12-01
scimago Q3
wos Q3
SJR: 0.334
CiteScore: 3.2
Impact factor: 1.5
ISSN: 00404039, 18733581
Organic Chemistry
Drug Discovery
Biochemistry
Abstract
The first stereoselective total synthesis of (−)-Inohanalactone is reported. The salient features of this synthesis are highly Z-selective Wittig olefination and chemoselective oxidation of 1,4 diol to the γ-butyrolactone. The synthesis was accomplished from readily available 2,3-O-isopropylidene- l -erythrose derived from d -ribose in eight steps with 32% overall yield.
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GOST
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Sharma K., Surineni N., Gholap S. L. First stereoselective total synthesis of (−)-Inohanalactone // Tetrahedron Letters. 2020. Vol. 61. No. 50. p. 152608.
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Sharma K., Surineni N., Gholap S. L. First stereoselective total synthesis of (−)-Inohanalactone // Tetrahedron Letters. 2020. Vol. 61. No. 50. p. 152608.
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RIS
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TY - JOUR
DO - 10.1016/j.tetlet.2020.152608
UR - https://doi.org/10.1016/j.tetlet.2020.152608
TI - First stereoselective total synthesis of (−)-Inohanalactone
T2 - Tetrahedron Letters
AU - Sharma, Kapil
AU - Surineni, Naresh
AU - Gholap, Shivajirao L
PY - 2020
DA - 2020/12/01
PB - Elsevier
SP - 152608
IS - 50
VL - 61
SN - 0040-4039
SN - 1873-3581
ER -
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BibTex (up to 50 authors)
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@article{2020_Sharma,
author = {Kapil Sharma and Naresh Surineni and Shivajirao L Gholap},
title = {First stereoselective total synthesis of (−)-Inohanalactone},
journal = {Tetrahedron Letters},
year = {2020},
volume = {61},
publisher = {Elsevier},
month = {dec},
url = {https://doi.org/10.1016/j.tetlet.2020.152608},
number = {50},
pages = {152608},
doi = {10.1016/j.tetlet.2020.152608}
}
Cite this
MLA
Copy
Sharma, Kapil, et al. “First stereoselective total synthesis of (−)-Inohanalactone.” Tetrahedron Letters, vol. 61, no. 50, Dec. 2020, p. 152608. https://doi.org/10.1016/j.tetlet.2020.152608.