Total synthesis of sanjoinine-G1

Byung Hoon Han; Yong Chul Kim; Man Ki Park; Jeong Hill Park; Hyun Jung Go; Hyun Ok Yang; Dae Yeon Suh; Young Hwa Kang

doi:10.3987/com-95-7142

Total synthesis of sanjoinine-G1

Byung Hoon Han, Yong Chul Kim, Man Ki Park, Jeong Hill Park, Hyun Jung Go, Hyun Ok Yang, Dae Yeon Suh, Young Hwa Kang

Department of Horticultural Science

Seoul National University

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

30 Scopus citations

Abstract

Sanjoinine-G1 (1), a 14-membered cyclopeptide, was synthesized with stereoselective reactions. Started from d-serine, a cyclic precursor for various frangulanine type 14-membered cyclopeptide alkaloids was synthesized and the side chain acylation product was identical with the natural sanjoinine-G1 (17 steps, overall yield 1.36%).

Original language	English
Pages (from-to)	1909-1914
Number of pages	6
Journal	Heterocycles
Volume	41
Issue number	9
DOIs	https://doi.org/10.3987/com-95-7142
State	Published - 1 Sep 1995

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title = "Total synthesis of sanjoinine-G1",

abstract = "Sanjoinine-G1 (1), a 14-membered cyclopeptide, was synthesized with stereoselective reactions. Started from d-serine, a cyclic precursor for various frangulanine type 14-membered cyclopeptide alkaloids was synthesized and the side chain acylation product was identical with the natural sanjoinine-G1 (17 steps, overall yield 1.36\%).",

author = "Han, \{Byung Hoon\} and Kim, \{Yong Chul\} and Park, \{Man Ki\} and Park, \{Jeong Hill\} and Go, \{Hyun Jung\} and Yang, \{Hyun Ok\} and Suh, \{Dae Yeon\} and Kang, \{Young Hwa\}",

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doi = "10.3987/com-95-7142",

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AU - Han, Byung Hoon

AU - Kim, Yong Chul

AU - Park, Man Ki

AU - Park, Jeong Hill

AU - Go, Hyun Jung

AU - Yang, Hyun Ok

AU - Suh, Dae Yeon

AU - Kang, Young Hwa

PY - 1995/9/1

Y1 - 1995/9/1

N2 - Sanjoinine-G1 (1), a 14-membered cyclopeptide, was synthesized with stereoselective reactions. Started from d-serine, a cyclic precursor for various frangulanine type 14-membered cyclopeptide alkaloids was synthesized and the side chain acylation product was identical with the natural sanjoinine-G1 (17 steps, overall yield 1.36%).

AB - Sanjoinine-G1 (1), a 14-membered cyclopeptide, was synthesized with stereoselective reactions. Started from d-serine, a cyclic precursor for various frangulanine type 14-membered cyclopeptide alkaloids was synthesized and the side chain acylation product was identical with the natural sanjoinine-G1 (17 steps, overall yield 1.36%).

UR - https://www.scopus.com/pages/publications/0000077645

U2 - 10.3987/com-95-7142

DO - 10.3987/com-95-7142

M3 - Article

AN - SCOPUS:0000077645

SN - 0385-5414

VL - 41

SP - 1909

EP - 1914

JO - Heterocycles

JF - Heterocycles

IS - 9

ER -

Total synthesis of sanjoinine-G1

Abstract

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