Erratum: Corrected Structure of Natural Hyacinthacine C1 via Total Synthesis (Journal of Natural Products (2019) 82: 2 (358−367) DOI: 10.1021/acs.jnatprod.8b00879)

Anthony W. Carroll; Anthony C. Willis; Masako Hoshino; Atsushi Kato; Stephen G. Pyne

doi:10.1021/acs.jnatprod.0c00389

Erratum: Corrected Structure of Natural Hyacinthacine C₁ via Total Synthesis (Journal of Natural Products (2019) 82: 2 (358−367) DOI: 10.1021/acs.jnatprod.8b00879)

Anthony W. Carroll, Anthony C. Willis, Masako Hoshino, Atsushi Kato, Stephen G. Pyne^*

^*Corresponding author for this work

Hospital Pharmacy

Research output: Contribution to journal › Comment/debate

Abstract

Metrics & More. Article Recommendations. Page 365, For the synthesis of (3aR,4R,6R,7R,8S,8aS,8bS)-7,8-Bisbenzyloxy-6-[(benzyloxy)-methyl]-4-methylhexahydro-4H-[1,3,2]dioxathiolo[4,5-a]-pyrrolizine 2,2-dioxide (26), the reagent SOCl2 should be replaced by SO2Cl2. This reagent (SO2Cl2) is correctly shown in the Scheme. The correct text is: (3aR,4R,6R,7R,8S,8aS,8bS)-7,8-Bisbenzyloxy-6-[(benzyloxy)-methyl]-4-methylhexahydro-4H-[1,3,2]dioxathiolo[4,5-a]-pyrrolizine 2,2-dioxide (26). To a solution of the diol 25 (25 mg, 0.0511 mmol) in anhydrous CH2Cl2 (5 mL) under a nitrogen atmosphere was added at 0 °C Et3 N (18 μL, 0.128 mmol), then SO2Cl2 (1.0 M solution in CH2Cl2, 0.0766 μL, 0.0766 mmol) dropwise.

Original language	English
Pages (from-to)	1733
Number of pages	1
Journal	Journal of Natural Products
Volume	83
Issue number	5
DOIs	https://doi.org/10.1021/acs.jnatprod.0c00389
State	Published - 2020/05/22

ASJC Scopus subject areas

Analytical Chemistry
Molecular Medicine
Pharmacology
Pharmaceutical Science
Drug Discovery
Complementary and alternative medicine
Organic Chemistry

Access to Document

10.1021/acs.jnatprod.0c00389

Cite this

@article{f90cf19a39b5477aadb32780147b2af2,

title = "Erratum: Corrected Structure of Natural Hyacinthacine C1 via Total Synthesis (Journal of Natural Products (2019) 82: 2 (358−367) DOI: 10.1021/acs.jnatprod.8b00879)",

abstract = "Metrics & More. Article Recommendations. Page 365, For the synthesis of (3aR,4R,6R,7R,8S,8aS,8bS)-7,8-Bisbenzyloxy-6-[(benzyloxy)-methyl]-4-methylhexahydro-4H-[1,3,2]dioxathiolo[4,5-a]-pyrrolizine 2,2-dioxide (26), the reagent SOCl2 should be replaced by SO2Cl2. This reagent (SO2Cl2) is correctly shown in the Scheme. The correct text is: (3aR,4R,6R,7R,8S,8aS,8bS)-7,8-Bisbenzyloxy-6-[(benzyloxy)-methyl]-4-methylhexahydro-4H-[1,3,2]dioxathiolo[4,5-a]-pyrrolizine 2,2-dioxide (26). To a solution of the diol 25 (25 mg, 0.0511 mmol) in anhydrous CH2Cl2 (5 mL) under a nitrogen atmosphere was added at 0 °C Et3 N (18 μL, 0.128 mmol), then SO2Cl2 (1.0 M solution in CH2Cl2, 0.0766 μL, 0.0766 mmol) dropwise.",

author = "Carroll, {Anthony W.} and Willis, {Anthony C.} and Masako Hoshino and Atsushi Kato and Pyne, {Stephen G.}",

note = "Publisher Copyright: {\textcopyright} 2020 American Chemical Society and American Society of Pharmacognosy.",

year = "2020",

month = may,

day = "22",

doi = "10.1021/acs.jnatprod.0c00389",

language = "英語",

volume = "83",

pages = "1733",

journal = "Journal of Natural Products",

issn = "0163-3864",

publisher = "American Chemical Society",

number = "5",

}

TY - JOUR

T1 - Erratum

T2 - Corrected Structure of Natural Hyacinthacine C1 via Total Synthesis (Journal of Natural Products (2019) 82: 2 (358−367) DOI: 10.1021/acs.jnatprod.8b00879)

AU - Carroll, Anthony W.

AU - Willis, Anthony C.

AU - Hoshino, Masako

AU - Kato, Atsushi

AU - Pyne, Stephen G.

PY - 2020/5/22

Y1 - 2020/5/22

N2 - Metrics & More. Article Recommendations. Page 365, For the synthesis of (3aR,4R,6R,7R,8S,8aS,8bS)-7,8-Bisbenzyloxy-6-[(benzyloxy)-methyl]-4-methylhexahydro-4H-[1,3,2]dioxathiolo[4,5-a]-pyrrolizine 2,2-dioxide (26), the reagent SOCl2 should be replaced by SO2Cl2. This reagent (SO2Cl2) is correctly shown in the Scheme. The correct text is: (3aR,4R,6R,7R,8S,8aS,8bS)-7,8-Bisbenzyloxy-6-[(benzyloxy)-methyl]-4-methylhexahydro-4H-[1,3,2]dioxathiolo[4,5-a]-pyrrolizine 2,2-dioxide (26). To a solution of the diol 25 (25 mg, 0.0511 mmol) in anhydrous CH2Cl2 (5 mL) under a nitrogen atmosphere was added at 0 °C Et3 N (18 μL, 0.128 mmol), then SO2Cl2 (1.0 M solution in CH2Cl2, 0.0766 μL, 0.0766 mmol) dropwise.

AB - Metrics & More. Article Recommendations. Page 365, For the synthesis of (3aR,4R,6R,7R,8S,8aS,8bS)-7,8-Bisbenzyloxy-6-[(benzyloxy)-methyl]-4-methylhexahydro-4H-[1,3,2]dioxathiolo[4,5-a]-pyrrolizine 2,2-dioxide (26), the reagent SOCl2 should be replaced by SO2Cl2. This reagent (SO2Cl2) is correctly shown in the Scheme. The correct text is: (3aR,4R,6R,7R,8S,8aS,8bS)-7,8-Bisbenzyloxy-6-[(benzyloxy)-methyl]-4-methylhexahydro-4H-[1,3,2]dioxathiolo[4,5-a]-pyrrolizine 2,2-dioxide (26). To a solution of the diol 25 (25 mg, 0.0511 mmol) in anhydrous CH2Cl2 (5 mL) under a nitrogen atmosphere was added at 0 °C Et3 N (18 μL, 0.128 mmol), then SO2Cl2 (1.0 M solution in CH2Cl2, 0.0766 μL, 0.0766 mmol) dropwise.

UR - http://www.scopus.com/inward/record.url?scp=85084312835&partnerID=8YFLogxK

U2 - 10.1021/acs.jnatprod.0c00389

DO - 10.1021/acs.jnatprod.0c00389

M3 - コメント/討論

C2 - 32315182

AN - SCOPUS:85084312835

SN - 0163-3864

VL - 83

SP - 1733

JO - Journal of Natural Products

JF - Journal of Natural Products

IS - 5

ER -