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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