Reptilian chemistry: Enantioselective syntheses of novel components from a crocodile exocrine secretion

Z. Yang; A. B. Attygalle; J. Meinwald

doi:10.1055/s-2000-8229

Reptilian chemistry: Enantioselective syntheses of novel components from a crocodile exocrine secretion

Z. Yang, A. B. Attygalle, J. Meinwald

Department of Chemistry and Chemical Biology

Cornell University

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

8 Scopus citations

Abstract

Enantioselective syntheses of the two naturally-occurring diastereomers of dianeackerone (1a and 1b) and of a closely related steroidal β-oxo ester (2), characterized from the paracloacal glandular secretion of the African dwarf crocodile, Osteolaemus tetraspis, are described.

Original language	English
Pages (from-to)	1936-1943
Number of pages	8
Journal	Synthesis
Issue number	13
DOIs	https://doi.org/10.1055/s-2000-8229
State	Published - 2000

Keywords

Crocodile
Dianeackerone
Enantioselective alkylation
Natural products
Steroids

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10.1055/s-2000-8229

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title = "Reptilian chemistry: Enantioselective syntheses of novel components from a crocodile exocrine secretion",

abstract = "Enantioselective syntheses of the two naturally-occurring diastereomers of dianeackerone (1a and 1b) and of a closely related steroidal β-oxo ester (2), characterized from the paracloacal glandular secretion of the African dwarf crocodile, Osteolaemus tetraspis, are described.",

keywords = "Crocodile, Dianeackerone, Enantioselective alkylation, Natural products, Steroids",

author = "Z. Yang and Attygalle, \{A. B.\} and J. Meinwald",

year = "2000",

doi = "10.1055/s-2000-8229",

language = "English",

pages = "1936--1943",

number = "13",

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TY - JOUR

T1 - Reptilian chemistry

T2 - Enantioselective syntheses of novel components from a crocodile exocrine secretion

AU - Yang, Z.

AU - Attygalle, A. B.

AU - Meinwald, J.

PY - 2000

Y1 - 2000

N2 - Enantioselective syntheses of the two naturally-occurring diastereomers of dianeackerone (1a and 1b) and of a closely related steroidal β-oxo ester (2), characterized from the paracloacal glandular secretion of the African dwarf crocodile, Osteolaemus tetraspis, are described.

AB - Enantioselective syntheses of the two naturally-occurring diastereomers of dianeackerone (1a and 1b) and of a closely related steroidal β-oxo ester (2), characterized from the paracloacal glandular secretion of the African dwarf crocodile, Osteolaemus tetraspis, are described.

KW - Crocodile

KW - Dianeackerone

KW - Enantioselective alkylation

KW - Natural products

KW - Steroids

UR - https://www.scopus.com/pages/publications/0033694262

UR - https://www.scopus.com/inward/citedby.url?scp=0033694262&partnerID=8YFLogxK

U2 - 10.1055/s-2000-8229

DO - 10.1055/s-2000-8229

M3 - Article

AN - SCOPUS:0033694262

SN - 0039-7881

SP - 1936

EP - 1943

JO - Synthesis

JF - Synthesis

IS - 13

ER -

Reptilian chemistry: Enantioselective syntheses of novel components from a crocodile exocrine secretion

Abstract

Keywords

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