Total Synthesis of (+)-Erogorgiaene using Lithiation-Borylation Methodology, and Stereoselective Synthesis of Each of its Diastereoisomers

TG Elford; S Nave; RP Sonawane; VK Aggarwal

doi:10.1021/ja207869f

Total Synthesis of (+)-Erogorgiaene using Lithiation-Borylation Methodology, and Stereoselective Synthesis of Each of its Diastereoisomers

TG Elford, S Nave, RP Sonawane, VK Aggarwal

School of Chemistry

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

63 Citations (Scopus)

Translated title of the contribution	Total Synthesis of (+)-Erogorgiaene using Lithiation-Borylation Methodology, and Stereoselective Synthesis of Each of its Diastereoisomers
Original language	English
Pages (from-to)	16798 - 16801
Journal	Journal of the American Chemical Society
Volume	133
DOIs	https://doi.org/10.1021/ja207869f
Publication status	Published - 2011

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10.1021/ja207869f

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NEW ASSYMETRIC REACTIONS AND THEIR APPLICATION IN TOTAL SYNTHESIS
Aggarwal, V. K. (Principal Investigator)
1/10/05 → 1/10/10
Project: Research

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title = "Total Synthesis of (+)-Erogorgiaene using Lithiation-Borylation Methodology, and Stereoselective Synthesis of Each of its Diastereoisomers",

author = "TG Elford and S Nave and RP Sonawane and VK Aggarwal",

year = "2011",

doi = "10.1021/ja207869f",

language = "English",

volume = "133",

pages = "16798 -- 16801",

journal = "Journal of the American Chemical Society",

issn = "1520-5126",

publisher = "American Chemical Society",

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T1 - Total Synthesis of (+)-Erogorgiaene using Lithiation-Borylation Methodology, and Stereoselective Synthesis of Each of its Diastereoisomers

AU - Elford, TG

AU - Nave, S

AU - Sonawane, RP

AU - Aggarwal, VK

PY - 2011

Y1 - 2011

U2 - 10.1021/ja207869f

DO - 10.1021/ja207869f

M3 - Article (Academic Journal)

C2 - 21936552

SN - 1520-5126

VL - 133

SP - 16798

EP - 16801

JO - Journal of the American Chemical Society

JF - Journal of the American Chemical Society

ER -

Total Synthesis of (+)-Erogorgiaene using Lithiation-Borylation Methodology, and Stereoselective Synthesis of Each of its Diastereoisomers

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Projects

NEW ASSYMETRIC REACTIONS AND THEIR APPLICATION IN TOTAL SYNTHESIS

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